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	<title>LABOKLIN aktuell 2020 &#8211; LABOKLIN Europe</title>
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		<title>Function and significance of certain electrolytes and their informative value: sodium (Na), potassium (K) and chloride (Cl)</title>
		<link>https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-sodium-na-potassium-k-and-chloride-cl/</link>
		
		<dc:creator><![CDATA[Laboklin &#124; Bad Kissingen]]></dc:creator>
		<pubDate>Tue, 13 Oct 2020 09:30:33 +0000</pubDate>
				<category><![CDATA[LABOKLIN aktuell 2020]]></category>
		<guid isPermaLink="false">https://staging.laboklin.com/int/en/?p=1301633</guid>

					<description><![CDATA[Sodium is the most important cation in the extracellular fluid. Hence, it is essential for maintaining osmolality or the distribution of water between the extracellular space (ECS) and the intracellular space (ICS).]]></description>
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			<h2>Sodium (Na)</h2>
<p>Sodium is the most important cation in the extracellular fluid. Hence, it is essential for maintaining osmolality or the distribution of water between the extracellular space (ECS) and the intracellular space (ICS). Hypo- and hypernatraemia occur when the sodium/water ratio in the ECS shifts towards water or sodium. This is often caused by an increase or decrease in total body water without an absolute change in electrolytes. But since Na is the main component of osmotically active substances in the ECS, hypo- and hypernatraemia are associated with changes in osmolality.</p>
<p>Na is the major electrolyte in the ECS and potassium (K) in the ICS. This asymmetric distribution of the electrolytes across the cell membrane requires active exchange of both cations by the Na/K-ATPase.</p>
<p>As a result, body fluids are in osmotic equilibrium. The distribution of water between the ECS and the ICS is normally constant and only shows slight fluctuations of just 1 – 2%. Acute changes in serum Na concentration which are not accompanied by a corresponding change in intracellular K concentration cause permeation of water from the ECS to the ICS. Cellular oedema occurs.</p>
<p>Concentrations of Na in serum and in the interstitial fluid are almost identical. Na causes about 95% of the osmotic pressure. The organism regulates the plasma Na concentration by adjusting the water content of the ECS and keeping the total body Na and Na in serum constant within a narrow range. This is done by drinking or by renal excretion of free water.</p>
<p>&nbsp;</p>
<h2>Examples of diseases and causes which can lead to hyponatraemia</h2>
<p>(Tab. 1)</p>
<p>&nbsp;</p>
<h2 class="bodytext">Examples of diseases and causes which can lead to hypernatraemia</h2>
<p>(Tab. 2)</p>
<p>&nbsp;</p>
<h2 class="bodytext">Potassium (K)</h2>
<p>In terms of quantity, potassium is the most important intracellular cation. More than 98% of the potassium in the body is found inside the cells. The serum potassium concentration is regulated within narrow limits. It is very important for membrane potentials; disorders of potassium balance lead to dysfunctions of skeletal muscles, heart and nerve cells. Potassium homeostasis is regulated by oral intake, distribution between the ECS and the ICS and renal elimination.</p>
<p>The regulation by the Na/K-ATPase is an important control mechanism for the movement of potassium between the ECS and the ICS. About 90% of the potassium is excreted via the kidneys, only a small part via the intestines.</p>
<p>Even though the plasma K concentration is only a moderate indicator of total body potassium, it is physiologically important for assessing the transmembrane electrochemical gradient.</p>

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<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-sodium-na-potassium-k-and-chloride-cl/table-1-examples-of-diseases-and-causes-which-can-lead-to-hyponatraemia/'><img fetchpriority="high" decoding="async" width="300" height="210" src="https://laboklin.com/wp-content/uploads/2020/10/Table-1-Examples-of-diseases-and-causes-which-can-lead-to-hyponatraemia-300x210.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of diseases and causes which can lead to hyponatraemia" srcset="https://laboklin.com/wp-content/uploads/2020/10/Table-1-Examples-of-diseases-and-causes-which-can-lead-to-hyponatraemia-300x210.jpg 300w, https://laboklin.com/wp-content/uploads/2020/10/Table-1-Examples-of-diseases-and-causes-which-can-lead-to-hyponatraemia-768x538.jpg 768w, https://laboklin.com/wp-content/uploads/2020/10/Table-1-Examples-of-diseases-and-causes-which-can-lead-to-hyponatraemia.jpg 964w" sizes="(max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-sodium-na-potassium-k-and-chloride-cl/table-2-examples-of-diseases-and-causes-which-can-lead-to-hypernatraemia/'><img decoding="async" width="300" height="94" src="https://laboklin.com/wp-content/uploads/2020/10/Table-2-Examples-of-diseases-and-causes-which-can-lead-to-hypernatraemia-300x94.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of diseases and causes which can lead to hypernatraemia" srcset="https://laboklin.com/wp-content/uploads/2020/10/Table-2-Examples-of-diseases-and-causes-which-can-lead-to-hypernatraemia-300x94.jpg 300w, https://laboklin.com/wp-content/uploads/2020/10/Table-2-Examples-of-diseases-and-causes-which-can-lead-to-hypernatraemia-768x240.jpg 768w, https://laboklin.com/wp-content/uploads/2020/10/Table-2-Examples-of-diseases-and-causes-which-can-lead-to-hypernatraemia.jpg 964w" sizes="(max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-sodium-na-potassium-k-and-chloride-cl/table-3-examples-of-diseases-and-conditions-which-can-lead-to-hypokalaemia/'><img decoding="async" width="300" height="116" src="https://laboklin.com/wp-content/uploads/2020/10/Table-3-Examples-of-diseases-and-conditions-which-can-lead-to-hypokalaemia-300x116.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of diseases and conditions which can lead to hypokalaemia" srcset="https://laboklin.com/wp-content/uploads/2020/10/Table-3-Examples-of-diseases-and-conditions-which-can-lead-to-hypokalaemia-300x116.jpg 300w, https://laboklin.com/wp-content/uploads/2020/10/Table-3-Examples-of-diseases-and-conditions-which-can-lead-to-hypokalaemia-768x298.jpg 768w, https://laboklin.com/wp-content/uploads/2020/10/Table-3-Examples-of-diseases-and-conditions-which-can-lead-to-hypokalaemia.jpg 966w" sizes="(max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-sodium-na-potassium-k-and-chloride-cl/table-4-examples-of-diseases-and-conditions-which-can-lead-to-hyperkalaemia/'><img loading="lazy" decoding="async" width="300" height="132" src="https://laboklin.com/wp-content/uploads/2020/10/Table-4-Examples-of-diseases-and-conditions-which-can-lead-to-hyperkalaemia-300x132.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of diseases and conditions which can lead to hyperkalaemia" srcset="https://laboklin.com/wp-content/uploads/2020/10/Table-4-Examples-of-diseases-and-conditions-which-can-lead-to-hyperkalaemia-300x132.jpg 300w, https://laboklin.com/wp-content/uploads/2020/10/Table-4-Examples-of-diseases-and-conditions-which-can-lead-to-hyperkalaemia-768x338.jpg 768w, https://laboklin.com/wp-content/uploads/2020/10/Table-4-Examples-of-diseases-and-conditions-which-can-lead-to-hyperkalaemia.jpg 966w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-sodium-na-potassium-k-and-chloride-cl/figure-1-chloride-fractions/'><img loading="lazy" decoding="async" width="300" height="260" src="https://laboklin.com/wp-content/uploads/2020/10/Figure-1-Chloride-fractions-300x260.jpg" class="attachment-medium size-medium" alt="Laboklin: Chloride fractions" srcset="https://laboklin.com/wp-content/uploads/2020/10/Figure-1-Chloride-fractions-300x260.jpg 300w, https://laboklin.com/wp-content/uploads/2020/10/Figure-1-Chloride-fractions.jpg 497w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-sodium-na-potassium-k-and-chloride-cl/table-5-example-of-diseases-associated-with-an-increase-in-serum-chloride/'><img loading="lazy" decoding="async" width="300" height="24" src="https://laboklin.com/wp-content/uploads/2020/10/Table-5-Example-of-diseases-associated-with-an-increase-in-serum-chloride-300x24.jpg" class="attachment-medium size-medium" alt="Laboklin: Example of diseases associated with an increase in serum chloride" srcset="https://laboklin.com/wp-content/uploads/2020/10/Table-5-Example-of-diseases-associated-with-an-increase-in-serum-chloride-300x24.jpg 300w, https://laboklin.com/wp-content/uploads/2020/10/Table-5-Example-of-diseases-associated-with-an-increase-in-serum-chloride-768x61.jpg 768w, https://laboklin.com/wp-content/uploads/2020/10/Table-5-Example-of-diseases-associated-with-an-increase-in-serum-chloride.jpg 966w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-sodium-na-potassium-k-and-chloride-cl/table-6-examples-of-diseases-associated-with-a-decrease-in-serum-chloride/'><img loading="lazy" decoding="async" width="300" height="63" src="https://laboklin.com/wp-content/uploads/2020/10/Table-6-Examples-of-diseases-associated-with-a-decrease-in-serum-chloride-300x63.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of diseases associated with a decrease in serum chloride" srcset="https://laboklin.com/wp-content/uploads/2020/10/Table-6-Examples-of-diseases-associated-with-a-decrease-in-serum-chloride-300x63.jpg 300w, https://laboklin.com/wp-content/uploads/2020/10/Table-6-Examples-of-diseases-associated-with-a-decrease-in-serum-chloride-768x161.jpg 768w, https://laboklin.com/wp-content/uploads/2020/10/Table-6-Examples-of-diseases-associated-with-a-decrease-in-serum-chloride.jpg 966w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>


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			<h2>Examples of diseases and conditions which can lead to hypokalaemia</h2>
<p>(Tab. 3)</p>
<p>&nbsp;</p>
<h2 class="bodytext">Examples of diseases and conditions which can lead to hyperkalaemia</h2>
<p>(Tab. 4)</p>
<p>&nbsp;</p>
<h2>Chloride (Cl)</h2>
<p class="bodytext">Chloride is one of the most important anions in the ECS. To a large extent, it is bound to sodium and present as common salt (NaCl). As a counterion of Na, it plays an important role in maintaining the water distribution between the ECS and the ICS, hence, in the plasma osmolality.</p>
<p class="bodytext">As a vital electrolyte, more than half of the chloride is found in the ECS (about 55%), approximately one third in the bones (about 30%) and only a small part inside the cells (about 15%).</p>
<p>&nbsp;</p>
<h2>Chloride fractions</h2>
<p>Chloride is mainly taken in through common salt (sodium chloride) in food. It is excreted via the kidneys and regulated by the hormone aldosterone, which causes reabsorption of the anion if there is a lack of chloride (Fig. 1).</p>
<p>&nbsp;</p>
<h2>Example of diseases associated with an increase in serum chloride</h2>
<p>(Tab. 5)</p>
<p>&nbsp;</p>
<h2 class="bodytext">Examples of diseases associated with a decrease in serum chloride</h2>
<p>(Tab. 6)</p>
<p style="text-align: right;"><em>Dr. Anja Cölfen</em></p>

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			<p><strong><a href="https://laboklin.com/wp-content/uploads/2020/10/LA_Oktober_2020_ENG_FINAL.pdf" target="_blank" rel="noopener">Function and significance of certain electrolytes and their informative value: sodium (Na), potassium (K) and chloride (Cl)</a></strong></p>

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		<title>Function and significance of certain electrolytes and their informative value: calcium (Ca), phosphorus (P) and magnesium (Mg)</title>
		<link>https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-calcium-ca-phosphorus-p-and-magnesium-mg/</link>
		
		<dc:creator><![CDATA[Laboklin &#124; Bad Kissingen]]></dc:creator>
		<pubDate>Thu, 03 Sep 2020 13:09:05 +0000</pubDate>
				<category><![CDATA[LABOKLIN aktuell 2020]]></category>
		<guid isPermaLink="false">https://staging.laboklin.com/int/en/?p=1301732</guid>

					<description><![CDATA[98% of the calcium (Ca) is contained in the bones and ensures their stability. In addition, it is also important for blood coagulation and muscle contraction.]]></description>
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			<h2>Calcium</h2>
<p>98% of the calcium (Ca) is contained in the bones and ensures their stability. In addition, it is also important for blood coagulation and muscle contraction. It is ingested with the food: bones, bone meal and egg shells contain calcium. Calcium is excreted in urine, faeces and, to a small extent, in sweat. The calcium and phosphorus balance is regulated by absorption from the small intestine, incorporation in or demineralisation of the bones and renal excretion. Parathyroid hormone (PTH), which is produced in the parathyroid gland, plays a central role here.</p>
<p>Despite the influence of many exogenous factors, such as varying mineral supply, this regulatory system can maintain homeostasis for a long time. <strong>Especially calcium is regulated very tightly. This means that a calcium level which is not within the normal range should always be verified, even if it deviates only slightly. </strong>Determination of calcium in the blood: Calcium consists of 3 fractions: 50% as free or ionised calcium, 45% protein-bound calcium, 5% calcium bound to anions, particularly to P and citrate complex (Fig. 1).</p>
<h2>Protein-bound calcium (routine diagnostics)</h2>
<p>In serum, protein-bound calcium is often measured as it can be determined more easily than ionised calcium because it is less influenced by pre-analytics.</p>
<p>However, its concentration in serum is influenced by the total protein, especially albumin. A drop in albumin levels causes a decrease in serum calcium.</p>
<h2>Ionised calcium</h2>
<p>This is a better indicator of the biologically active calcium because serum or plasma concentrations are directly controlled by PTH and calcitriol. It is therefore the more sensitive method for measuring disturbances of calcium balance.</p>
<p>However, pre-analysis is much more complex. Ionised calcium can only be determined if collected under exclusion of air (sampling instructions are available from Laboklin).</p>
<p>&nbsp;</p>
<h2>Examples of hypocalcaemia</h2>
<p>(Tab. 1)</p>
<p>&nbsp;</p>
<h2>Examples of hypercalcaemia</h2>
<p>(Tab. 2)</p>

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<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-calcium-ca-phosphorus-p-and-magnesium-mg/figure-1-calcium-fractions/'><img loading="lazy" decoding="async" width="300" height="226" src="https://laboklin.com/wp-content/uploads/2020/09/Figure-1-Calcium-fractions-300x226.jpg" class="attachment-medium size-medium" alt="Laboklin: Calcium fractions" srcset="https://laboklin.com/wp-content/uploads/2020/09/Figure-1-Calcium-fractions-300x226.jpg 300w, https://laboklin.com/wp-content/uploads/2020/09/Figure-1-Calcium-fractions.jpg 456w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-calcium-ca-phosphorus-p-and-magnesium-mg/table-1-examples-of-hypocalcaemia/'><img loading="lazy" decoding="async" width="300" height="187" src="https://laboklin.com/wp-content/uploads/2020/09/Table-1-Examples-of-hypocalcaemia-300x187.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of hypocalcaemia" srcset="https://laboklin.com/wp-content/uploads/2020/09/Table-1-Examples-of-hypocalcaemia-300x187.jpg 300w, https://laboklin.com/wp-content/uploads/2020/09/Table-1-Examples-of-hypocalcaemia.jpg 763w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-calcium-ca-phosphorus-p-and-magnesium-mg/table-2-examples-of-hypercalcaemia/'><img loading="lazy" decoding="async" width="300" height="118" src="https://laboklin.com/wp-content/uploads/2020/09/Table-2-Examples-of-hypercalcaemia-300x118.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of hypercalcaemia" srcset="https://laboklin.com/wp-content/uploads/2020/09/Table-2-Examples-of-hypercalcaemia-300x118.jpg 300w, https://laboklin.com/wp-content/uploads/2020/09/Table-2-Examples-of-hypercalcaemia.jpg 763w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-calcium-ca-phosphorus-p-and-magnesium-mg/table-3-examples-of-hypophosphataemia/'><img loading="lazy" decoding="async" width="300" height="102" src="https://laboklin.com/wp-content/uploads/2020/09/Table-3-Examples-of-hypophosphataemia-300x102.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of hypophosphataemia" srcset="https://laboklin.com/wp-content/uploads/2020/09/Table-3-Examples-of-hypophosphataemia-300x102.jpg 300w, https://laboklin.com/wp-content/uploads/2020/09/Table-3-Examples-of-hypophosphataemia.jpg 765w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-calcium-ca-phosphorus-p-and-magnesium-mg/table-4-examples-of-hyperphosphataemia-physiological-in-young-animals/'><img loading="lazy" decoding="async" width="300" height="48" src="https://laboklin.com/wp-content/uploads/2020/09/Table-4-Examples-of-hyperphosphataemia-physiological-in-young-animals-300x48.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of hyperphosphataemia (physiological in young animals)" srcset="https://laboklin.com/wp-content/uploads/2020/09/Table-4-Examples-of-hyperphosphataemia-physiological-in-young-animals-300x48.jpg 300w, https://laboklin.com/wp-content/uploads/2020/09/Table-4-Examples-of-hyperphosphataemia-physiological-in-young-animals.jpg 765w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/function-and-significance-of-certain-electrolytes-and-their-informative-value-calcium-ca-phosphorus-p-and-magnesium-mg/table-5-examples-of-hypomagnesaemia/'><img loading="lazy" decoding="async" width="300" height="64" src="https://laboklin.com/wp-content/uploads/2020/09/Table-5-Examples-of-hypomagnesaemia-300x64.jpg" class="attachment-medium size-medium" alt="Laboklin: Examples of hypomagnesaemia" srcset="https://laboklin.com/wp-content/uploads/2020/09/Table-5-Examples-of-hypomagnesaemia-300x64.jpg 300w, https://laboklin.com/wp-content/uploads/2020/09/Table-5-Examples-of-hypomagnesaemia.jpg 765w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>


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			<h2>Inorganic phosphorus (P)</h2>
<p>The terms phosphorus and phosphate are used interchangeably in laboratory medicine. For clinical purposes, this is irrelevant because the phosphate content is measured as inorganic phosphorus. 85% of the phosphate is located in the bones in combination with calcium and 14% exists intracellularly. There, it is present as an anion or as a component of lipids, proteins and nucleic acids. 1% of the P content is located in plasma or in other body fluids, yet in most pathological conditions, the concentration in serum correlates with the phosphate content of the body. Renal reabsorption is an important indicator of the phosphate level in the serum. If phosphate absorption is increased or GFR is decreased, renal reabsorption is decreased. Renal reabsorption is regulated by fibroblast growth factor (FGF) and parathyroid hormone.</p>
<p>&nbsp;</p>
<h2>Examples of hypophosphataemia</h2>
<p>(Tab. 3)</p>
<p>&nbsp;</p>
<h2>Hyperphosphataemia</h2>
<p>Hyperphosphataemia lowers the concentration of 1.25(OH) vit D and increases the secretion of PTH and FGF. These hormones have a phosphaturic effet.</p>
<p>&nbsp;</p>
<h2>Examples of hyperphosphataemia (physiological in young animals)</h2>
<p>(Tab. 4)</p>
<p>&nbsp;</p>
<h2>Magnesium</h2>
<p>1% of the magnesium (Mg) is found in the extracellular fluid. The Mg fractions in serum and plasma are present as ionised magnesium, protein-bound magnesium, mostly to albumin, and complex-bound magnesium in form of salt. The skeletal system, the gastrointestinal tract and the kidneys regulate the magnesium concentration in the plasma. Magnesium depends on the albumin concentration and the pH value. If there is alkalosis, the Mg level is reduced by increased protein binding. However, a reduction may also be seen with normal serum levels. Magnesium has many different tasks: It is essential for electrolyte balance, energy metabolism (activation of ATP), neural conduction, protein synthesis, bone matrix formation and mineralisation of the skeleton as well as for cell division.</p>
<p>&nbsp;</p>
<h2>Examples of hypomagnesaemia</h2>
<p>(Tab. 5)</p>
<p>&nbsp;</p>
<h2>Hypermagnesaemia</h2>
<p>Except for severe CRI, hypermagnesaemia is unlikely to occur with adequate substitution.</p>
<h2>Serum electrolytes and nutrition</h2>
<p>When evaluating serum electrolytes, special attention should be paid to nutrition. Calcium is only ingested with the food through bones, bone meal and egg shells. Muscles and innards, vegetables and fruit are significantly lower in calcium. Ca deficiency in the diet results in increased PTH secretion. This leads to mobilisation of Ca from the bones and increased absorption from the intestine. In the long term, bone demineralisation develops and even bone deformation, particularly of the long bones, as well as other changes in the skeletal system. A typical sign is the so-called “rubber jaw&#8221;. Ca oversupply, on the other hand, which occurs much less frequently for nutritional reasons, leads to tissue calcification, stomach ulcers and impaired muscle contraction up to tetany. Severely disturbed bone metabolism, especially in the long bones, and increased urinary excretion of calcium are signs of Ca oversupply. Phosphate is present in many food products (meat, vegetables and fat). This means that phosphorus intake from food is usually sufficient. Phosphate is stored in the skeletal system and regulated by the kidneys. Food should have a Ca/P ratio of 2:1 or maybe 1.5:1. Inadequate supply, even inverse Ca/P ratios, are often seen in individual rations. Magnesium is mainly found in green vegetables, nuts, cereals, seafood and meat. But also drinking water, especially hard water, contains magnesium.</p>
<h2>Conclusion</h2>
<p>Concerning serum levels and nutrition, it is particularly important to note that serum levels in the normal range do not necessarily reflect a balanced diet. Serum electrolyte levels in the reference range do not imply that the ration sufficiently meets the needs for these parameters. A balanced ration calculation is required instead.</p>
<p class="bodytext" style="text-align: right;"><i>Dr. Anja Cölfen</i></p>

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			<p><strong><a href="https://laboklin.com/wp-content/uploads/2020/09/LA_September_2020_EN_FINAL.pdf" target="_blank" rel="noopener">Function and significance of certain electrolytes and their informative value: calcium (Ca), phosphorus (P) and magnesium (Mg)</a></strong></p>

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		<title>Diarrhoeal diseases in rabbits and guinea pigs –  laboratory diagnostic options</title>
		<link>https://laboklin.com/en/diarrhoeal-diseases-in-rabbits-and-guinea-pigs-laboratory-diagnostic-options/</link>
		
		<dc:creator><![CDATA[Laboklin &#124; Bad Kissingen]]></dc:creator>
		<pubDate>Tue, 18 Aug 2020 14:56:13 +0000</pubDate>
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					<description><![CDATA[Diarrhoeal diseases are a common problem in small mammals. As in other animal species, too, diarrhoea is characterised by defaecation with higher water content and/or increased frequency.]]></description>
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			<p>Diarrhoeal diseases are a common problem in small mammals. As in other animal species, too, diarrhoea is characterised by defaecation with higher water content and/or increased frequency. Especially in rabbits, it is not uncommon for the owner to confuse cecotropes with diarrhoea – here, a typical preliminary report is “intermittent diarrhoea”. Misinterpretation can also occur in obese, weakened and/or ataxic/paretic animals which are not able to reingest their cecotropes, as well as in cases of urinary contamination of the anogenital region.</p>
<p>The causes of diarrhoea are manifold, but can easily be determined with thorough and structured diagnostic workup.</p>
<p>A complete medical history (duration, course, amount, admixtures) should always be taken at first, followed by a full clinical examination (weight, adspection, auscultation, palpation). In order to exclude gastrointestinal causes, a targeted faecal examination is the best diagnostic option and therefore the method of choice when working up a diarrhoeal disease. If extragastrointestinal causes (organic, metabolic-toxic, neoplastic) are suspected, a haematological blood test should be carried out, the clinical-chemical parameters should be determined and, if necessary, imaging techniques should be used (Fig.1).<sup>1</sup></p>
<h2>Faecal examination</h2>
<p>The collection of faecal samples is very simple. To facilitate the collection, use as little absorbent bedding as possible. For shipment to a laboratory, it is recommended to use suitable sample containers (1 sample tube per animal, approx. ¾ full) and to send them in an appropriate outer packaging to ensure hygienic shipment (Fig. 2).</p>
<h2>Diagnostic options in the veterinary practice/fresh faeces</h2>
<p>In the practice, you can already get a first indication of the cause of diarrhoea if you carry out a macroscopic faecal analysis (species-specific size and shape as well as colour, consistency and admixtures) and also examine the fresh (!) faecal sample microscopically directly on site.</p>

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<a href='https://laboklin.com/en/diarrhoeal-diseases-in-rabbits-and-guinea-pigs-laboratory-diagnostic-options/figure-1-causes-of-diarrhoea-in-rabbits-and-guinea-pigs-gp-modified-after-hein-2017/'><img loading="lazy" decoding="async" width="300" height="196" src="https://laboklin.com/wp-content/uploads/2020/08/Figure-1-Causes-of-diarrhoea-in-rabbits-and-guinea-pigs-GP-modified-after-Hein-2017-300x196.jpg" class="attachment-medium size-medium" alt="Laboklin: Causes of diarrhoea in rabbits and guinea pigs (GP) (modified after Hein 2017)" srcset="https://laboklin.com/wp-content/uploads/2020/08/Figure-1-Causes-of-diarrhoea-in-rabbits-and-guinea-pigs-GP-modified-after-Hein-2017-300x196.jpg 300w, https://laboklin.com/wp-content/uploads/2020/08/Figure-1-Causes-of-diarrhoea-in-rabbits-and-guinea-pigs-GP-modified-after-Hein-2017-768x501.jpg 768w, https://laboklin.com/wp-content/uploads/2020/08/Figure-1-Causes-of-diarrhoea-in-rabbits-and-guinea-pigs-GP-modified-after-Hein-2017.jpg 956w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/diarrhoeal-diseases-in-rabbits-and-guinea-pigs-laboratory-diagnostic-options/figure-2-faeces-tube-with-outer-packaging/'><img loading="lazy" decoding="async" width="300" height="279" src="https://laboklin.com/wp-content/uploads/2020/08/Figure-2-Faeces-tube-with-outer-packaging-300x279.jpg" class="attachment-medium size-medium" alt="Laboklin: Faeces tube with outer packaging" srcset="https://laboklin.com/wp-content/uploads/2020/08/Figure-2-Faeces-tube-with-outer-packaging-300x279.jpg 300w, https://laboklin.com/wp-content/uploads/2020/08/Figure-2-Faeces-tube-with-outer-packaging.jpg 329w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/diarrhoeal-diseases-in-rabbits-and-guinea-pigs-laboratory-diagnostic-options/table-1-endoparasites-in-rabbits-and-guinea-pigs/'><img loading="lazy" decoding="async" width="300" height="149" src="https://laboklin.com/wp-content/uploads/2020/08/Table-1-Endoparasites-in-rabbits-and-guinea-pigs-300x149.jpg" class="attachment-medium size-medium" alt="Laboklin: Endoparasites in rabbits and guinea pigs" srcset="https://laboklin.com/wp-content/uploads/2020/08/Table-1-Endoparasites-in-rabbits-and-guinea-pigs-300x149.jpg 300w, https://laboklin.com/wp-content/uploads/2020/08/Table-1-Endoparasites-in-rabbits-and-guinea-pigs-768x381.jpg 768w, https://laboklin.com/wp-content/uploads/2020/08/Table-1-Endoparasites-in-rabbits-and-guinea-pigs.jpg 955w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/diarrhoeal-diseases-in-rabbits-and-guinea-pigs-laboratory-diagnostic-options/table-2-pathogenic-bacteria-in-rabbits-and-guinea-pigs/'><img loading="lazy" decoding="async" width="300" height="56" src="https://laboklin.com/wp-content/uploads/2020/08/Table-2-Pathogenic-bacteria-in-rabbits-and-guinea-pigs-300x56.jpg" class="attachment-medium size-medium" alt="Laboklin: Pathogenic bacteria in rabbits and guinea pigs" srcset="https://laboklin.com/wp-content/uploads/2020/08/Table-2-Pathogenic-bacteria-in-rabbits-and-guinea-pigs-300x56.jpg 300w, https://laboklin.com/wp-content/uploads/2020/08/Table-2-Pathogenic-bacteria-in-rabbits-and-guinea-pigs-768x143.jpg 768w, https://laboklin.com/wp-content/uploads/2020/08/Table-2-Pathogenic-bacteria-in-rabbits-and-guinea-pigs.jpg 955w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>


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			<p><strong>Fresh specimen</strong></p>
<p>For a fresh specimen, a pea-sized amount of fresh faeces is usually sufficient. With – ideally warm – physiological saline solution or water, a faecal suspension is prepared. For the microscopic examination, a drop is placed on a slide and covered with a cover glass. Testing from a smaller sample quantity is generally possible, but carries the risk of reduced sensitivity.</p>
<p>Yeasts, such as <em>Cyniclomyces guttulatus</em>, as well as protozoa (Tab. 1) and occasionally worm eggs can be detected very well in the fresh specimen.</p>
<p>One of the most frequent causes of diarrhoea is dysbiosis – a shift in the rather gram-positive intestinal flora towards more gram-negative bacteria, clostridia and yeasts. Causes are often of dietary origin (inappropriate feeding, resulting in a lack of crude fibres and/or excess carbohydrates), any kind of malpositioned teeth or even parasitosis. A first and quick indication of a dysbiotic condition is the increased occurrence of yeast (&gt;15/visual field) at 100-fold magnification.</p>
<p>Although flagellates, such as giardia, can be diagnosed in fresh faeces, they are very rarely found. Such findings in fresh faecal samples are only conclusive in positive cases. A more suitable test procedure for this is the giardia ELISA.</p>
<h2>Tape test method</h2>
<p>The tape test method – perianal tape impression using adhesive strips – is a quick and simple test method which may as well be carried out on site. It is particularly recommended for the detection of oxyurid eggs and larvae (<em>Passalurus ambiguus</em>). Detection by flotation is often negative, as oxyurid eggs tend to sink due to their high density. Sometimes, however, larval fragments of <em>Passalurus ambiguus</em> can be found in the flotation.</p>
<h2>Pooled faeces</h2>
<p>A 3-day pooled faecal sample generally increases the sensitivity of the faecal analysis for parasites (except for flagellates). When submitting faecal samples from rabbits or guinea pigs, different test methods are available: flotation, sedimentation (SAFC method), bacteriological examination, giardia ELISA and PCR (pathogen specific).</p>
<p><strong>Flotation</strong></p>
<p>The principle of the flotation test is based on the fact that parasite stages with a low density are transported to the surface of solutions which have a higher specific gravity. In rabbits and guinea pigs, this test method is suitable for the enrichment of coccidian oocysts as well as for the enrichment of species-specific nematode and cestode eggs (Tab. 1) and can be carried out in the practice, too, using commercially available test kits.</p>
<p><strong>Sedimentation</strong></p>
<p>During sedimentation, parasite stages with a high density settle in the sediment of a lighter solution. With this test method, especially trematode eggs (<em>Fasciola hepatica</em>, <em>Dicrocoelium dendriticum</em>) can be detected in rabbits. To some extent, the detection of nematode eggs is also possible, although flotation is to be preferred here due to its higher sensitivity. Trematode eggs have not yet been described in guinea pigs.</p>
<p><strong>Bacteriological examination</strong></p>
<p>The culture of faecal bacteria provides information on the pathogenesis and allows for targeted treatment through the creation of an antibiogram. Rabbits and guinea pigs as herbivorous caecal digesters physiologically have a mainly gram-positive flora with several hundred different bacterial species, yeasts, anaerobes and protozoa. Pathogen differentiation with a subsequent creation of an antibiogram is advisable for them, especially in food-producing animals and if human pathogenic organisms are suspected, but is of little use in the typical cases of diet-induced dysbiosis.</p>
<p>Shifts towards a gram-negative intestinal flora should always be considered in the context of feeding mistakes and/or parasitosis. This is because the detection of a certain species of bacteria is no proof that it is the actual cause of diarrhoea – except for pathogenic bacteria (particularly toxigenic ones) (Tab. 2).</p>
<p><strong>Polymerase chain reaction</strong></p>
<p>Polymerase chain reaction (PCR) is a method for the detection of specific pathogens, such as <em>Lawsonia intracellularis</em>. The advantage is its high sensitivity, the disadvantage is that it must be known beforehand which pathogen to look for and that only a positive result confirms it. A negative result cannot completely rule out an infection.</p>
<h2>Blood test</h2>
<p>Diarrhoea in rabbits and guinea pigs may also have extragastrointestinal causes. Depending on the animal species, various causes need to be considered, such as organic, metabolic or toxic disorders as well as hypovolaemia or neoplasia (Fig. 1). A blood test (Rodent Profile incl. a complete blood count) covers almost all differential diagnoses and should thus be part of the routine diagnosis of diarrhoea if the previous faecal examination was negative.</p>
<p>During the haematological examination of dysbiotic patients and patients with diarrhoea, a so-called pseudo left shift (shift from lymphocytic to neutrophil blood count) is often seen. Here, too, a differential blood count can help in making a diagnosis. In guinea pigs, leukocytosis with lymphocytosis indicates lymphoma and eosinophilia indicates parasitosis as a possible cause of diarrhoea. Unfortunately, this is not the case in rabbits; they usually have aleukaemic lymphoma and do not show eosinophilia due to parasites. A blood test is also suitable to clarify organic-metabolic or endocrine causes of diarrhoea (e.g. hyperthyroidism in guinea pigs). Hepatopathies (GLDH, AST, ALT, bilirubin, bile acids, triglycerides, cholesterol) and nephropathies (urea, creatinine) as a cause of diarrhoea as well as electrolyte shifts (Na, K, P), protein losses (total protein, albumin) and/or blood losses (erythrocyte count, haematocrit, total protein, albumin, urea) can easily be determined.</p>
<p>A blood test may also be very helpful in serious conditions such as ileus or obstruction: The glucose level serves as a prognostic factor in this case. The higher the level, the more likely it is that ileus is the cause and the worse the prognosis.<sup>2</sup> If sodium is additionally considered in the interpretation, an even more precise prognosis can be made, because additional hyponatraemia doubles the mortality rate.<sup>3</sup></p>
<h2>Conlcusion</h2>
<p>The faecal analysis combined with a haematological and clinical-chemical examination covers almost all the differential diagnoses of a diarrhoeal disease and can thus serve to initiate quick and targeted treatment.</p>

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			<h5 class="bodytext"><b>Literatur:</b></h5>
<ul>
<li>
<h6><span style="color: #808080;"><strong><sup>1</sup><i>Hein J. (2017): Durchfallerkrankungen bei Kleinsäugern. </i><i>Hannover, Schlütersche.</i></strong></span></h6>
</li>
<li>
<h6><span style="color: #808080;"><strong><sup>2</sup><i>Harcourt-Brown F M, Harcourt-Brown S F (2012): </i><i>Clinical value of blood glucose measurement in pet </i><i>rabbits. Vet Rec., 170(26):674.</i></strong></span></h6>
</li>
<li>
<h6><span style="color: #808080;"><strong><sup>3</sup><i>Bonvehi C et al. (2014): Prevalence and types of hyponatraemia, </i><i>its relationship with hyperglycaemia and </i><i>mortality in ill pet rabbits. Vet Rec., 174(22):554.</i></strong></span></h6>
</li>
</ul>

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			<p><strong><a href="https://laboklin.com/wp-content/uploads/2020/08/La_August_2020_EN_FINAL-.pdf" target="_blank" rel="noopener">Diarrhoeal diseases in rabbits and guinea pigs – laboratory diagnostic options</a></strong></p>

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		<title>Laboratory tests for dogs and cats with behavioural problems</title>
		<link>https://laboklin.com/en/laboratory-tests-for-dogs-and-cats-with-behavioural-problems/</link>
		
		<dc:creator><![CDATA[Laboklin &#124; Bad Kissingen]]></dc:creator>
		<pubDate>Sun, 05 Jul 2020 11:30:44 +0000</pubDate>
				<category><![CDATA[LABOKLIN aktuell 2020]]></category>
		<guid isPermaLink="false">https://staging.laboklin.com/int/en/?p=1301782</guid>

					<description><![CDATA[Patients who display unwanted behaviour are normally only presented to the practice late in their history of suffering, since behaviour is usually not associated with an illness, but solely with the animal’s circumstances and its nature.]]></description>
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			<h2>If it is not a matter of education</h2>
<p>Patients who display unwanted behaviour are normally only presented to the practice late in their history of suffering, since behaviour is usually not associated with an illness, but solely with the animal’s circumstances and its nature (Fig. 1).</p>
<p>However, abnormal behaviour can be caused by a wide variety of disorders. Increased aggressiveness can, for example, be caused by pain or hormones, but also infectious diseases – think of rabies, at worst – should be considered.</p>
<p>To differentiate, possible organic, hormonal, infectious, orthopaedic, genetic, autoimmune and allergic causes should be clarified. Furthermore, poisoning can also lead to problematic behaviour.</p>
<p>Among the many possible causes, the most common underlying diseases in our clinical laboratory consultation are listed here.</p>
<h2>Organic diseases</h2>
<p><strong>Liver:</strong> Patients with portosystemic shunt may be presented to the practice for the first time because of apathy. Even if the affected dogs start behaving conspicuously by showing circular movements or by having epileptiform seizures, symptoms can be significantly milder and less specific, especially in case of an intrahepatic shunt. Clinical chemistry can become challenging as not all shunt patients show changes in liver values. Frequently, an isolated increase in ALT is observed. Diagnosis should thus be made by means of a bile acid stimulation test or – if possible in-house – by measuring ammonia and also include an ultrasound scan.</p>
<p><strong>Kidney and bladder:</strong> Diseases affecting these organs can also lead to unwanted behaviour. If, for example, puppies show signs of uncleanliness, congenital or acquired kidney or bladder problems should be considered, too. In addition to medical imaging, a urinalysis (status/sediment and urine culture) as well as the determination of the protein-creatinine ratio (UPC) are recommended. The determination of urea, creatinine and SDMA in serum is not always effective in puppies, as the growing organism has highly variable concentrations of these substrates in serum. Adult cats may show kidney-related uncleanliness which is often misinterpreted as a behavioural problem.</p>

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<a href='https://laboklin.com/en/laboratory-tests-for-dogs-and-cats-with-behavioural-problems/figure-1-game-or-aggression/'><img loading="lazy" decoding="async" width="300" height="300" src="https://laboklin.com/wp-content/uploads/2020/07/Figure-1-Game-or-aggression-300x300.jpg" class="attachment-medium size-medium" alt="Laboklin: &quot;Game or aggression&quot;?" srcset="https://laboklin.com/wp-content/uploads/2020/07/Figure-1-Game-or-aggression-300x300.jpg 300w, https://laboklin.com/wp-content/uploads/2020/07/Figure-1-Game-or-aggression-150x150.jpg 150w, https://laboklin.com/wp-content/uploads/2020/07/Figure-1-Game-or-aggression.jpg 366w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/laboratory-tests-for-dogs-and-cats-with-behavioural-problems/figure-2-abnormal-and-normal-behaviour/'><img loading="lazy" decoding="async" width="300" height="160" src="https://laboklin.com/wp-content/uploads/2020/07/Figure-2-Abnormal-and-normal-behaviour-300x160.jpg" class="attachment-medium size-medium" alt="Laboklin: Effect of a leck of serotonin to the behaviour" srcset="https://laboklin.com/wp-content/uploads/2020/07/Figure-2-Abnormal-and-normal-behaviour-300x160.jpg 300w, https://laboklin.com/wp-content/uploads/2020/07/Figure-2-Abnormal-and-normal-behaviour.jpg 372w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/laboratory-tests-for-dogs-and-cats-with-behavioural-problems/table-1-primary-laboratory-parameters-to-be-determined-relating-to-the-most-common-behavioural-problems/'><img loading="lazy" decoding="async" width="300" height="266" src="https://laboklin.com/wp-content/uploads/2020/07/Table-1-Primary-laboratory-parameters-to-be-determined-relating-to-the-most-common-behavioural-problems-300x266.jpg" class="attachment-medium size-medium" alt="Laboklin: Primary laboratory parameters to be determined relating to the most common behavioural problems" srcset="https://laboklin.com/wp-content/uploads/2020/07/Table-1-Primary-laboratory-parameters-to-be-determined-relating-to-the-most-common-behavioural-problems-300x266.jpg 300w, https://laboklin.com/wp-content/uploads/2020/07/Table-1-Primary-laboratory-parameters-to-be-determined-relating-to-the-most-common-behavioural-problems.jpg 763w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>


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			<h2>Hormonal imbalances</h2>
<p>Behaviour is regulated by a variety of hormones and hormonal interactions. Changes in a single hormone level can trigger profound behavioural changes.</p>
<p><strong>Thyroid gland:</strong> Diseases of the thyroid gland frequently occur in dogs and cats. In dogs, both cause and symptoms differ with age. In young dogs, it is autoimmune thyroiditis which leads to behavioural changes, whereas in older dogs these changes are caused by follicular atrophy.</p>
<p>In young dogs, anxious or aggressive behaviour with hyperactivity and severe educational problems is often associated with thyroid dysfunction. If these patients really suffer from thyroid-related behavioural problems, these are due to initial episodes of <strong>autoimmune thyroiditis</strong> with fluctuating hormone secretions. The diagnosis is confirmed by measuring the T4 and TSH levels but, above all, by determining the thyroglobulin antibodies (TgAb) as well as T3- and T4-antibodies.</p>
<p>In older dogs, <strong>hypothyroidism</strong> is one of the most common known endocrine disorders. Some of the first changes that are observed are increasing reluctance to move and lethargy. As the function of the thyroid gland can be influenced by many other diseases, it is necessary to determine the T4 and TSH levels and to rule out other conditions in order to confirm the diagnosis.</p>
<p>The clinical signs triggered by <strong>hyperthyroidism</strong> in older cats (weight loss, hyperactivity) often lead to a quick diagnosis. Only rarely, hyperthyroid cats are apathetic. In most cases, measuring the T4 level in serum is sufficient; in uncertain cases, TSH can be measured.</p>
<p><strong>Gonads/adrenal gland:</strong> Sex steroids are responsible for a complex system of behaviours. The <strong>castration</strong> of domesticated animals and, thus, the suppression of gonadal function is frequently performed and significantly influences the behaviour. Not only the reproductive ability but especially aggressive behaviour against conspecifics should be suppressed. In case of dominance problems, it is also expected that castration will make it easier to guide the dogs.</p>
<p>If the dog or the cat continues to show sexual behaviour despite being neutered, the question arises as to whether there is still some gonadal tissue present. Determining the luteinising hormone (LH) as well as steroid hormones and particularly the measurement of the anti-Müllerian hormone (AMH) level in both male and female animals can help to answer this question.</p>
<p>Endocrine <strong>neoplasms</strong> can also manifest themselves through behavioural change. In the early phase, this may even be the only clinical sign. <strong>Sertoli cell tumours</strong> cause male dogs to become attractive to other males and to behave more like being neutered due to increased oestrogen secretion. <strong>Granulosa cell tumours</strong> in female dogs can mimic the behaviour of a pregnant bitch with nest-building behaviour and carrying around soft toys if hormone secretion, especially progesterone, is low but constant. It is alarming for the owner that no previous heat was observed and, thus, a false pregnancy is unlikely.</p>
<p>Endocrine active adrenal tumours lead to various behavioural changes depending on the hormonal secretion pattern. While <strong>Cushing’s syndrome</strong>, which is common in dogs, is primarily associated with increased appetite up to allotriophagia, other tumours of the adrenal cortex are rare. A rather common tumour of the adrenal medulla is the catecholamine-secreting <strong>phaeochromocytoma</strong>. The permanently elevated level of catecholamine in the blood results in increased restlessness and anxiety in patients. Determining the catecholamines normetanephrine and metanephrine in blood plasma or the normetanephrine- and metanephrine-creatinine ratio in urine helps to confirm the diagnosis.</p>
<h2>Neurotransmitters</h2>
<p>Recently, clinical laboratory testing of dogs with behavioural problems has started to focus on the “happiness hormone” <strong>serotonin</strong>. Serotonin is a neurotransmitter whose effects in the CNS include the inhibition of fear and aggression. A lack of serotonin in the CNS therefore leads to fearful-aggressive behaviour. Although serotonin cannot cross the blood-brain barrier, low serotonin levels in the blood correlate with certain behavioural problems. This correlation has been confirmed by our own research (Fig. 2).</p>
<p>Therefore, measuring serotonin in serum is recommended for dogs with fearful-aggressive behaviour. In addition to food supplementation with tryptophan, treatment can be carried out with serotonin analogues or serotonin reuptake inhibitors. A return to normal behaviour can be expected after a few weeks.</p>
<h2>Infectious causes</h2>
<p>It is the tactic of some infectious agents to manipulate their host’s behaviour with the aim of being transferred to a new host more quickly. A typical example for this is an infection with the rabies virus. Fortunately, rabies only plays a very minor role in Germany. Nevertheless, it may be a differential diagnosis in animals from uncontrolled imports and should be considered if dogs are aggressive.</p>
<p>But even less dramatic and much more frequent infections can also lead to behavioural changes. Especially ectoparasites living in the fur or on the skin can lead to increased restlessness without causing massive itching at the same time. Infected hair can be sent in to identify the parasite.</p>
<h2>Poisoning</h2>
<p>The intake of foreign substances is another way in which unwanted behaviour can be triggered. Lead poisoning manifests itself in various ways with restlessness, agitation, increased barking or biting and depression. If the dog ingests nicotine through cigarette butts, it leads to agitation and hyperactivity. It also frequently happens that animals take drugs if the owner does not handle the drugs carefully. Depending on the drug and dosage, behaviour can vary and range from hyperexcitability to somnolence. A single intake of poison results in a sudden change in behaviour and, at a higher dose, is usually associated with further symptoms.</p>
<h2>Genetic behavioural problems</h2>
<p>Particularly in pedigree animals, there are various genetic defects that are associated with behavioural change. These include, for example, neuronal ceroid lipofuscinosis (restlessness, aggressiveness, anxiety), acral mutilation syndrome (paw chewing), glycogen storage disease (lethargy), necrotising meningoencephalitis (disorientation, head shaking, circling), dopamine transporter polymorphism (hereditary behavioural abnormality in Malinois dogs: reduced excitability, episodic aggression) and many more. The causative mutations have already been identified in numerous breeds, which is why the option of diagnosing hereditary diseases in pedigree dogs with behavioural problems should also be taken into account. Especially for dogs, we offer an extensive and constantly growing range of tests. For more information, see <a href="https://shop.labogen.com/" target="_blank" rel="noopener">https://shop.labogen.com/</a></p>
<p>Primary laboratory parameters to be determined relating to the most common behavioural problems (Tab. 1).</p>
<p>(1)  Send in cooled (possibly frozen) and protected from light<br />
(2)  Frozen EDTA plasma, urine acidified with HCI to pH &lt; 2, send in frozen and protected from light<br />
(3)  EDTA whole blood<br />
(4)  Only possible from urine; always state clinical history.</p>
<p style="text-align: right;"><em>Dr. Ruth Klein</em></p>

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			<p><strong><a href="https://laboklin.com/wp-content/uploads/2020/07/LA_Juli_2020_EN.pdf" target="_blank" rel="noopener">Laboratory tests for dogs and cats with behavioural problems</a></strong></p>

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		<title>Introducing the “Feline Travel Profile”</title>
		<link>https://laboklin.com/en/introducing-the-feline-travel-profile/</link>
		
		<dc:creator><![CDATA[Laboklin &#124; Bad Kissingen]]></dc:creator>
		<pubDate>Tue, 12 May 2020 08:50:15 +0000</pubDate>
				<category><![CDATA[LABOKLIN aktuell 2020]]></category>
		<guid isPermaLink="false">https://staging.laboklin.com/int/en/?p=1301803</guid>

					<description><![CDATA[In Germany, vector-borne infections are becoming more important in dogs and cats for the following reasons ...]]></description>
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			<p>In Germany, vector-borne infections are becoming more important in dogs and cats for the following reasons:</p>
<ul>
<li>Import of dogs and cats from abroad.</li>
<li>Increase in tourism and transport of goods in Europe and worldwide.</li>
<li>Changes in climate.</li>
</ul>
<p>As a result of global warming, vectors which were previously endemic in warmer regions of the Mediterranean or in Southeastern Europe may be able to survive all year round in countries in Central and Northern Europe, such as Germany, and may even establish stable transmission cycles. Since April 2012, we have been offering a “Feline Travel Profile” for cats with suspected vector-borne infections related to a medical history of being abroad. This profile has been established in our range of services for cats that were imported into Germany from Mediterranean countries or Southeastern Europe or which have stayed in these countries as a travel companion (Fig. 1).</p>
<p>The “Feline Travel Profile” includes direct PCR detection of dirofilaria and hepatozoon and indirect antibody IFAT detection of leishmania, ehrlichia and rickettsia. More than a quarter of the cats (172/606; 28.4%) tested positive for at least one pathogen (Tab. 1).</p>
<h2>Description of the tested pathogens</h2>
<p><span style="color: #000000;"><em><strong>Hepatozoonosis</strong></em></span></p>
<p><em>Hepatozoon (H.) felis</em> is most frequently found in cats worldwide. In Europe, the pathogen has been detected in ticks (<em>Rhipicephalus sanguineus</em>, <em>Ixodes hexagonus</em>) and fleas (<em>Ctenocephalides felis</em>). The vector competence in cats is unclear. Transplacental infections with <em>H. felis</em> have also been described in cats. Recently, a first case report about an autochthonous infection with <em>H. felis</em> in a clinically affected domestic cat in Austria was published. Hepatozoonosis should, thus, also be considered in cats which have not had a history of staying abroad.</p>

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<a href='https://laboklin.com/en/introducing-the-feline-travel-profile/figure-1-number-of-cats-tested-between-042012-and-122019-using-the-feline-travel-profile-with-the-percentage-of-cats-tested-positive-per-year/'><img loading="lazy" decoding="async" width="300" height="206" src="https://laboklin.com/wp-content/uploads/2020/05/Figure-1-Number-of-cats-tested-between-042012-and-122019-using-the-Feline-Travel-Profile-with-the-percentage-of-cats-tested-positive-per-year-300x206.jpg" class="attachment-medium size-medium" alt="Laboklin: Number of cats tested between 04/2012 and 12/2019 using the “Feline Travel Profile” with the percentage of cats tested positive per year." srcset="https://laboklin.com/wp-content/uploads/2020/05/Figure-1-Number-of-cats-tested-between-042012-and-122019-using-the-Feline-Travel-Profile-with-the-percentage-of-cats-tested-positive-per-year-300x206.jpg 300w, https://laboklin.com/wp-content/uploads/2020/05/Figure-1-Number-of-cats-tested-between-042012-and-122019-using-the-Feline-Travel-Profile-with-the-percentage-of-cats-tested-positive-per-year.jpg 705w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/introducing-the-feline-travel-profile/table-1-vector-borne-pathogens-in-the-feline-travel-profile-with-prevalence-in-the-period-042012-122019/'><img loading="lazy" decoding="async" width="300" height="205" src="https://laboklin.com/wp-content/uploads/2020/05/Table-1-Vector-borne-pathogens-in-the-Feline-Travel-Profile-with-prevalence-in-the-period-042012-–-122019-300x205.jpg" class="attachment-medium size-medium" alt="Laboklin: Vector-borne pathogens in the “Feline Travel Profile” with prevalence in the period 04/2012 – 12/2019." srcset="https://laboklin.com/wp-content/uploads/2020/05/Table-1-Vector-borne-pathogens-in-the-Feline-Travel-Profile-with-prevalence-in-the-period-042012-–-122019-300x205.jpg 300w, https://laboklin.com/wp-content/uploads/2020/05/Table-1-Vector-borne-pathogens-in-the-Feline-Travel-Profile-with-prevalence-in-the-period-042012-–-122019.jpg 707w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/introducing-the-feline-travel-profile/figure-2-collected-hard-tick-symbolic-image/'><img loading="lazy" decoding="async" width="300" height="179" src="https://laboklin.com/wp-content/uploads/2020/05/Figure-2-Collected-hard-tick-symbolic-image-300x179.jpg" class="attachment-medium size-medium" alt="Laboklin: Collected hard tick (symbolic image)" srcset="https://laboklin.com/wp-content/uploads/2020/05/Figure-2-Collected-hard-tick-symbolic-image-300x179.jpg 300w, https://laboklin.com/wp-content/uploads/2020/05/Figure-2-Collected-hard-tick-symbolic-image.jpg 705w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>


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			<p><em><strong>Leishmaniasis</strong></em></p>
<p>In cats, <em>Leishmania infantum</em> is most likely transmitted by sand flies (<em>Phlebotomus spp.</em>). Dogs are considered the main reservoir, but cats can also become infected. However, it is assumed that cats are more resistant to infections than dogs. The pathogenesis of feline leishmaniasis is unclear, just like the role of the cat in the transmission cycle of the pathogen.</p>
<p>In cats, infections are often subclinical. When clinical signs occur, mainly nodular and ulcerative skin lesions are seen as well as enlarged lymph nodes, weight loss and ophthalmologic symptoms. To confirm infection, quantitative serological tests such as IFAT should be carried out in cats. In case titres are negative or low, a parasitological detection method (e.g. PCR, culture, histology, cytology) should be used to diagnose the pathogen if there is a clinical suspicion as seroconversion of the pathogen may be delayed for years.</p>
<p><em><strong>Ehrlichiosis</strong></em></p>
<p>In Europe, <em>Ehrlichia (E.) canis</em> is transmitted by the tick <em>Rhipicephalus sanguineus</em>. In Germany, the vector can only survive temporarily within certain temperature ranges or as populations in buildings heated throughout the year. Case studies on infections with <em>E. canis</em> in cats are rare and the clinical picture is non-specific. A single positive antibody detection by IFAT most likely indicates a pathogen contact in an endemic foreign country.</p>
<p><strong><em>Rickettsiosis/Mediterranean spotted fever</em></strong></p>
<p>More than 20 species belong to the “Spotted fever group”, with <em>Rickettsia conorii </em>being the most important zoonotic agent in Europe. <em>Rickettsia conorii </em>is transmitted by ticks (<em>Rhipicephalus sanguineus</em>) and can cause clinical signs in dogs; its significance in cats is not clear.</p>
<p><em>Rickettsia felis</em> is transmitted by fleas. Seroconversion occurs in cats after contact with infected fleas. Bacteraemia is assumed to be short, as cats with confirmed antibodies usually had negative PCR results in blood. Antibody detection was often positive in cats in which several vector-borne infectious agents were found. This also reflects what is known about pathogen detection in dogs or in human medicine.</p>
<p><em><strong>Dirofilariasis</strong></em></p>
<p><em>Diroflaria (D.) immitis </em>(heartworm) is a pathogenic species in cats, while <em>D. repens</em>, as the causative agent of subcutaneous dirofilariasis, also plays an important role as a zoonotic agent. Both pathogens are transmitted by mosquitoes. Prevalence in cats is only about one tenth of that in dogs. In cats, infections with <em>D. immitis</em> may be self-limiting, however, there may also be fatal courses with sudden death and clinical signs such as shortness of breath, coughing and vomiting. Yet, cats are more resistant than dogs and only occasionally develop transient microfilaraemia. Since larvae are only temporarily detectable in the blood and/or the number of larvae is below the detection limit of the <em>D. immitis</em> antigen detection test or the Knott’s test, false negative results often occur in cats. Heat treatment of the serum before performing the test increases the probability of pathogen detection.</p>
<p>We offer this method after prior consultation. Furthermore, a cardiac ultrasound should be performed to detect worms in the pulmonary artery as well as in the right atrium and the right ventricle of the heart. <em>Diroflaria repens</em> can cause skin lesions such as subcutaneous nodules.</p>
<p>Severe courses with itching, pustules, ulcerations and exfoliative dermatitis are rare. Microfilaria PCR has a low sensitivity in cats. If pathogen detection is positive, it should be followed by species differentiation to decide on the treatment (Fig. 2).</p>
<h2>Summary</h2>
<p>In cats with the appropriate medical history, vector contact and the respective clinical signs, vector-borne infections should also be considered in the differential diagnosis. Some vector-borne infections are probably underdiagnosed in cats. The role of the cat as a reservoir host and the clinical relevance of many vector-borne infections are not yet sufficiently understood. Preventive measures such as vector control throughout the year with suitable acaricidal and insecticidal preparations are also recommended for cats. The prepatent period of dirofilaria and leishmania is long. In case of negative test results within six months after import or return to Germany, it is thus recommended to repeat the test at the time when the cat has exclusively been in Germany for at least six months.</p>

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			<p><strong><a href="https://laboklin.com/wp-content/uploads/2020/05/LA_Mai_2020_EN.pdf" target="_blank" rel="noopener">Introducing the “Feline Travel Profile”</a></strong></p>

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		<title>Feline Upper Respiratory Disease</title>
		<link>https://laboklin.com/en/feline-upper-respiratory-disease/</link>
		
		<dc:creator><![CDATA[Laboklin &#124; Bad Kissingen]]></dc:creator>
		<pubDate>Mon, 20 Apr 2020 10:25:22 +0000</pubDate>
				<category><![CDATA[LABOKLIN aktuell 2020]]></category>
		<guid isPermaLink="false">https://staging.laboklin.com/int/en/?p=1301818</guid>

					<description><![CDATA[Infections with the various causative agents of feline upper respiratory disease complex occur regularly despite available vaccines.]]></description>
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			<p>Infections with the various causative agents of feline upper respiratory disease complex occur regularly despite available vaccines. Particularly with high population densities and the resulting high infection pressure, as is often the case in boarding or breeding catteries and animal shelters, the occurrence of diseases can be a serious problem. The five primary causative agents of feline upper respiratory disease are feline herpesvirus 1 (FHV1), feline calicivirus (FCV), <em>Chlamydia </em>(<em>C.</em>)<em> felis</em>,<em> Bordetella </em>(<em>B.</em>)<em> bronchiseptica</em> and <em>Mycoplasma</em> (<em>M.</em>) <em>felis</em>. The symptoms are manifold and can therefore often not be clearly assigned to one pathogen or the other. They can range from mild, watery nasal discharge to severe, fatal systemic disease. Rhinitis, conjunctivitis, lesions of the oral cavity and the cornea, fever and pneumonia are observed. In addition to the primary causative agents mentioned above, there are often non-specific secondary bacterial pathogens. Mixed infections with two or more different pathogens of the feline upper respiratory disease complex are common.</p>
<p><strong>Feline calicivirus</strong> is highly contagious, and due to its high variability and mutation rate, there are multiple virus variants with greatly varying virulence, some of which cause severe systemic disease with a high fatality rate. Symptoms depend on the virulence of the virus variant as well as on the immune status of the particular cat. Possible signs include ulcers in the oral cavity, problems with the upper respiratory tract, high fever and occasional lameness caused by transient arthritis. The virus is shed in oronasal and conjunctival secretions for up to four weeks and is transmitted both directly and indirectly. It is environmentally stable for a long time and remains infectious on dry surfaces for up to one month. Even after overcoming the disease, many cats continue to shed the virus, sometimes for several years. Virus detection by PCR is very sensitive, so that in individual cases, vaccine viruses are also detected which may be shed in very small quantities for a few weeks after vaccination. On the other hand, the high mutation rate of the virus can also lead to false negative results.</p>
<p>Following an infection with <strong>feline herpesvirus 1</strong>, the animals remain latent carriers of the virus for life. Stress or immunosuppression can lead to a reactivation of the disease. Symptoms consist of acute rhinitis and conjunctivitis with fever, blepharospasm and anorexia; especially in young cats, particularly severe pneumonia with fatal outcome may sometimes occur. Herpesviruses have been described as being associated with ulcerative dendritic keratitis and are considered the main cause of this disease. Symptoms normally subside after two weeks. The virus is usually only shed for a short period of time, in some cases up to three weeks, in oral, nasal and conjunctival secretions. PCR detection has a very high sensitivity and even very low-level shedders are reliably detected.</p>

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<a href='https://laboklin.com/en/feline-upper-respiratory-disease/abbildung-1-bearb/'><img loading="lazy" decoding="async" width="300" height="191" src="https://laboklin.com/wp-content/uploads/2020/04/Abbildung-1-bearb-300x191.jpg" class="attachment-medium size-medium" alt="Laboklin: Pathogens detected (%) in the Respiratory Profile I (cat) in 2018" srcset="https://laboklin.com/wp-content/uploads/2020/04/Abbildung-1-bearb-300x191.jpg 300w, https://laboklin.com/wp-content/uploads/2020/04/Abbildung-1-bearb.jpg 481w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/feline-upper-respiratory-disease/abbildung-2-bearb/'><img loading="lazy" decoding="async" width="300" height="199" src="https://laboklin.com/wp-content/uploads/2020/04/Abbildung-2-bearb-300x199.jpg" class="attachment-medium size-medium" alt="Laboklin: Number of different pathogens in mixed infections" srcset="https://laboklin.com/wp-content/uploads/2020/04/Abbildung-2-bearb-300x199.jpg 300w, https://laboklin.com/wp-content/uploads/2020/04/Abbildung-2-bearb.jpg 556w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/feline-upper-respiratory-disease/table-1-number-of-mixed-infections-in-the-respiratory-profile-i-cat-in-2018-total-number-of-samples-n-1897/'><img loading="lazy" decoding="async" width="300" height="52" src="https://laboklin.com/wp-content/uploads/2020/04/Table-1-Number-of-mixed-infections-in-the-Respiratory-Profile-I-cat-in-2018-total-number-of-samples-n-1897-300x52.jpg" class="attachment-medium size-medium" alt="Laboklin: Number of mixed infections in the Respiratory Profile I (cat) in 2018 (total number of samples n = 1897)" srcset="https://laboklin.com/wp-content/uploads/2020/04/Table-1-Number-of-mixed-infections-in-the-Respiratory-Profile-I-cat-in-2018-total-number-of-samples-n-1897-300x52.jpg 300w, https://laboklin.com/wp-content/uploads/2020/04/Table-1-Number-of-mixed-infections-in-the-Respiratory-Profile-I-cat-in-2018-total-number-of-samples-n-1897.jpg 515w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/feline-upper-respiratory-disease/table-2-mixed-infections-and-frequency-of-occurrence-of-the-individual-pathogens-of-feline-upper-respiratory-disease-fcv-fhv-chlamydia-mycoplasma-b-bronchiseptica-in-2018/'><img loading="lazy" decoding="async" width="300" height="146" src="https://laboklin.com/wp-content/uploads/2020/04/Table-2-Mixed-infections-and-frequency-of-occurrence-of-the-individual-pathogens-of-feline-upper-respiratory-disease-FCV-FHV-chlamydia-mycoplasma-B.-bronchiseptica-in-2018-300x146.jpg" class="attachment-medium size-medium" alt="Laboklin: Mixed infections and frequency of occurrence of the individual pathogens of feline upper respiratory disease (FCV, FHV, chlamydia, mycoplasma, B. bronchiseptica) in 2018" srcset="https://laboklin.com/wp-content/uploads/2020/04/Table-2-Mixed-infections-and-frequency-of-occurrence-of-the-individual-pathogens-of-feline-upper-respiratory-disease-FCV-FHV-chlamydia-mycoplasma-B.-bronchiseptica-in-2018-300x146.jpg 300w, https://laboklin.com/wp-content/uploads/2020/04/Table-2-Mixed-infections-and-frequency-of-occurrence-of-the-individual-pathogens-of-feline-upper-respiratory-disease-FCV-FHV-chlamydia-mycoplasma-B.-bronchiseptica-in-2018.jpg 741w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>


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			<p><strong><em>Chlamydia felis</em></strong> is an obligate intracellular bacterium and a common cause of acute and chronic conjunctivitis. Symptoms on the eye also include hyperaemia of the nictitating membrane and ocular discharge. However, keratitis and ulcerations are rather uncommon. If they occur, it indicates the involvement of feline herpesvirus. In some cases, infection with FHV1 is accompanied by fever, inappetence, weight loss and respiratory symptoms, and in pregnant animals, abortion may occur. According to the literature, young cats under 9 months of age are most frequently affected, which is confirmed by our data. Transmission occurs through close contact, as the bacterium cannot survive outside the host. Shedding of the pathogen can last up to 60 days, occasionally, an even longer, persistent infection is possible. In individual cases, <em>C. felis</em> can be transmitted to humans and cause conjunctivitis. PCR is the most sensitive method for detecting <em>C. felis.</em></p>
<p><strong>Mycoplasmas</strong> are considered part of the normal microflora of the upper respiratory tract. Nevertheless, <em>Mycoplasma felis</em> plays an important role as a pathogen in feline conjunctivitis. Mycoplasmas are less frequently involved in lower respiratory tract infections, although they can also cause severe pneumonia in individual cases. Only very rarely, <em>M. felis</em> shows zoonotic potential in immunocompromised people. It is difficult to culture mycoplasmas; that is why here, too, detection by PCR is the method of choice.</p>
<p>Contrary to dogs (kennel cough complex), <strong><em>Bordetella bronchiseptica</em></strong> only plays a minor role in cats. The bacterium is a primary pathogen that colonises the ciliated epithelium of the host. It is rarely found in the lower respiratory tract of cats, if so, mainly younger animals are affected. Still, every coughing cat should also be tested for <em>B. bronchiseptica</em>. Bordetella can be transmitted from dog to cat and a zoonotic potential cannot be excluded. In addition to swabs of the nasal mucosa and the oropharynx, bronchoalveolar lavage can also be examined. Bacterial culture as well as PCR are suitable methods. However, performing an antibiogram is only possible after culture. If the pathogen is detected in the lavage sample, it is seen as proof of infection.</p>
<h2>Diagnosis</h2>
<p>In general, PCR is considered the standard method for the detection of the causative agents of feline upper respiratory disease complex. Conjunctival, oral and/or pharyngeal swabs are suitable sample materials for the detection of viral infections, mycoplasma and chlamydia. Ocular swabs should always be taken <strong>BEFORE</strong> fluorescein or rose bengal are applied. As chlamydia replication is obligate intracellular, they cannot be detected by routine bacteriological methods. Infections with <em>Bordetella bronchiseptica</em> are rather rarely found in cats; a fast and sensitive PCR detection is possible here as well. Since there are often bacterial co-infections, especially in cases involving the eyes, but also in chronic respiratory tract infections, an additional swab with transport medium should be sent in for bacteriological examination including the creation of an antibiogram, in order to be able to initiate a suitable local and/or systemic therapy. For the diagnosis of feline upper respiratory disease, antibody detection is less useful, because many cats are vaccinated or have had pathogen contact as kittens.</p>
<p>Since most infections are often acute as well, it is usually the pathogens which can be detected at the onset of the disease, but not the antibodies that are produced in the further course of the disease. In the literature, it is stated that 80% of upper respiratory tract infections in cats are, above all, caused by FHV1 and FCV. Laboklin offers various PCR profiles for the detection of the most common pathogens of feline upper respiratory disease. Over the past years, in the Respiratory Profile I (FCV, FHV1, chlamydia, mycoplasma, <em>B. bronchiseptica</em>), mycoplasma was found to be the most prevalent pathogen (in up to 50% of the Respiratory Profiles that were examined), followed by calicivirus and herpesvirus (each in about 20% of cats examined). Infections with chlamydia (7 – 9%) and Bordetella (2 – 3%) play a minor role. In the vast majority of cases, Bordetella was found in mixed infections (94.7%), there were only 2 cases (5.3%) in which it was found as single infection.</p>
<p>In total, there were hardly any differences in the occurrence of individual pathogens in each of the years of the evaluated period between 2011 and 1018.</p>
<p>In 2018, 951 (50.1%) of the 1897 total samples for the Respiratory Profile 1 (cat) were positive for mycoplasma, 305 (16.1%) for FHV1, 333 (17.6%) for FCV, 128 (6.7%) for chlamydia and 38 (2%) for <em>B. bronchiseptica</em> (Fig. 1). Of these 1897 total samples, 450 (23.7%) showed mixed infections with two or more causative agents of feline upper respiratory disease (Table 1). Mixed infections of mycoplasma and FCV/FHV1 were most common, followed by infections with mycoplasma and chlamydia and mixed infections with both viruses (Fig. 2).</p>
<p><strong>Table 1: Number of mixed infections in the Respiratory Profile I (cat) in 2018 (total number of samples n = 1897)</strong></p>
<p><strong>Table 2: Mixed infections and frequency of occurrence of the individual pathogens of feline upper respiratory disease (FCV, FHV, chlamydia, mycoplasma, <em>B. bronchiseptica</em>) in 2018</strong></p>

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			<p><strong><a href="https://laboklin.com/wp-content/uploads/2020/04/LA_-Katzenschnupfen_April_2020_EN.pdf" target="_blank" rel="noopener">Feline Upper Respiratory Disease</a></strong></p>

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		<title>Chronic diarrhoea, flatulence and recurrent parasitosis – intestinal microbial disorders in dogs and cats</title>
		<link>https://laboklin.com/en/chronic-diarrhoea-flatulence-and-recurrent-parasitosis-intestinal-microbial-disorders-in-dogs-and-cats/</link>
		
		<dc:creator><![CDATA[Laboklin &#124; Bad Kissingen]]></dc:creator>
		<pubDate>Sat, 21 Mar 2020 15:26:10 +0000</pubDate>
				<category><![CDATA[LABOKLIN aktuell 2020]]></category>
		<guid isPermaLink="false">https://staging.laboklin.com/int/en/?p=1301855</guid>

					<description><![CDATA[The body of mammals is colonised with countless microorganisms such as bacteria, fungi, protozoa and viruses.]]></description>
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			<p class="bodytext">The body of mammals is colonised with countless microorganisms such as bacteria, fungi, protozoa and viruses. Colonised areas include the oral and nasal cavities, the surface of the skin as well as the mucous membranes of the urogenital and gastrointestinal tracts. The individuals that form this collective are called the microbiota, the accumulated genetic information of each individual microbe is called the microbiome. With 10<sup>11</sup> – 10<sup>12</sup> bacteria per g of faeces, the primary colonisation site of the microbiota is the colon. Of these bacteria, more than 99% are strictly anaerobic and, thus, make up the main part of the intestinal flora.</p>
<p class="bodytext">If someone wanted to examine the composition of this community more closely, there were almost only microbiological-cultural methods available until the end of the nineties. Culturable intestinal bacteria could be detected this way, however, with less than 1%, they just represent a very small proportion of all microbes in the intestine. Thus, the much larger proportion of non-culturable microbes remained largely unnoticed. Only the development of new test methods on a molecular biological basis (e.g. next-generation sequencing) made it possible to also detect bacteria that could not be microbiologically cultivated. Thanks to this approach, the intestinal microbiome could be examined in all its complexity for the first time, which led to a real microbiome boom in science. By now, numerous studies have proven that intestinal microbes definitely make an important contribution to the health of the human host.</p>
<p>The most important tasks of the intestinal flora include: utilisation and digestion of food, synthesis of essential micronutrients (e.g. vitamin B12), maintenance of the intestinal mucosal barrier, regulation of the intestine-associated immune system, defence against pathogens and opportunistic pathogens and promotion of healthy digestion and intestinal motility.</p>
<h2>Intestinal microbiome of dogs and cats</h2>
<p>Compared to the human intestinal microbiome, scientist rather seldom focus on the intestinal microbiome of small animals such as dogs and cats. The pathomechanisms initiated and/or promoted by dysbioses of the intestinal flora are very similar. More and more often, diseases like chronic diarrhoea, IBD, food allergy, metabolic disorders and atopic diseases are seen in the veterinary practice (Fig. 1).</p>
<p>In fact, studies by an American research group show that the differences between human and canine microbiome are much smaller than previously assumed. The genetic information of all intestinal bacteria is 63% identical in people and dogs. (In mice or pigs, by contrast, the similarity is much lower, at 20% and 33%). One reason often mentioned for this is the close social bond pet owners build with their pets. In addition to spatial proximity, there is often similar nutrition (e.g. feeding from the table), which significantly increases the probability of a horizontal transfer of bacteria in both directions. Further proof of this hypothesis is that the overlap of intestinal microbiomes from dog owners to their own pets is significantly higher than to foreign dogs that do not live in the same household.</p>
<p>It is still quite unclear whether such similarities of the intestinal microbiome also exist in dogs and cats. Is the intestinal flora of a dog with dysbiosis comparable to that of a cat? And if this is not the case: How does a dysbiotic condition of a dog differ from that of a cat?</p>

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<a href='https://laboklin.com/en/chronic-diarrhoea-flatulence-and-recurrent-parasitosis-intestinal-microbial-disorders-in-dogs-and-cats/abb1/'><img loading="lazy" decoding="async" width="300" height="225" src="https://laboklin.com/wp-content/uploads/2020/03/Abb1-300x225.jpg" class="attachment-medium size-medium" alt="Laboklin: High-grade chronic histiocytic to mixed-cell colitis in a Boxer (haematoxylin-eosin stain, 4x)." srcset="https://laboklin.com/wp-content/uploads/2020/03/Abb1-300x225.jpg 300w, https://laboklin.com/wp-content/uploads/2020/03/Abb1-768x576.jpg 768w, https://laboklin.com/wp-content/uploads/2020/03/Abb1.jpg 830w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/chronic-diarrhoea-flatulence-and-recurrent-parasitosis-intestinal-microbial-disorders-in-dogs-and-cats/abb2-bearb/'><img loading="lazy" decoding="async" width="300" height="207" src="https://laboklin.com/wp-content/uploads/2020/03/Abb2-bearb-300x207.jpg" class="attachment-medium size-medium" alt="Laboklin: Microflora composition in dogs with chronic diarrhoea compared with the clinically healthy control group (n = 30, * p&lt;0.05, Wilcoxon-Mann-Whitney test). (b) Microflora composition in clinically healthy dogs in comparison with clinically healthy cats (n = 27, * p&lt;0.05, Wilcoxon-­Mann­Whitney test)." srcset="https://laboklin.com/wp-content/uploads/2020/03/Abb2-bearb-300x207.jpg 300w, https://laboklin.com/wp-content/uploads/2020/03/Abb2-bearb-1024x708.jpg 1024w, https://laboklin.com/wp-content/uploads/2020/03/Abb2-bearb-768x531.jpg 768w, https://laboklin.com/wp-content/uploads/2020/03/Abb2-bearb.jpg 1240w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/chronic-diarrhoea-flatulence-and-recurrent-parasitosis-intestinal-microbial-disorders-in-dogs-and-cats/abb3-bearb/'><img loading="lazy" decoding="async" width="300" height="110" src="https://laboklin.com/wp-content/uploads/2020/03/Abb3-bearb-300x110.jpg" class="attachment-medium size-medium" alt="Laboklin: Microflora composition in cats with chronic diarrhoea compared with the clinically healthy control group (n = 27, * p&lt;0.05, Wilcoxon-­Mann­Whitney test)." srcset="https://laboklin.com/wp-content/uploads/2020/03/Abb3-bearb-300x110.jpg 300w, https://laboklin.com/wp-content/uploads/2020/03/Abb3-bearb-1024x375.jpg 1024w, https://laboklin.com/wp-content/uploads/2020/03/Abb3-bearb-768x281.jpg 768w, https://laboklin.com/wp-content/uploads/2020/03/Abb3-bearb.jpg 1244w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>
<a href='https://laboklin.com/en/chronic-diarrhoea-flatulence-and-recurrent-parasitosis-intestinal-microbial-disorders-in-dogs-and-cats/abb4-bearb/'><img loading="lazy" decoding="async" width="300" height="118" src="https://laboklin.com/wp-content/uploads/2020/03/Abb4-bearb-300x118.jpg" class="attachment-medium size-medium" alt="Laboklin: Copy numbers of lactobacilli, bifidobacteria and enterococci in clinically healthy dogs and cats as well as in dogs and cats with chronic diarrhoea " srcset="https://laboklin.com/wp-content/uploads/2020/03/Abb4-bearb-300x118.jpg 300w, https://laboklin.com/wp-content/uploads/2020/03/Abb4-bearb-1024x401.jpg 1024w, https://laboklin.com/wp-content/uploads/2020/03/Abb4-bearb-768x301.jpg 768w, https://laboklin.com/wp-content/uploads/2020/03/Abb4-bearb.jpg 1245w" sizes="auto, (max-width: 300px) 100vw, 300px" /></a>


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			<h2>Intestinal dysbiosis in dogs</h2>
<p>Our own studies, which compared the copy numbers of important anaerobic bacterial markers for intestinal dysbiosis in dogs with chronic diarrhoea and a clinically healthy control group by means of quantitative real-time PCR, show clear differences (Fig. 2a). Particularly noticeable is a significant reduction in the anaerobic, carbohydrate-digesting intestinal flora, the saccharolytic bacteria (<em>Faecalibacterium prausnitzii</em>, <em>Blautia spp.</em>, <em>Turicibacter spp.</em>). An important function of these groups of bacteria is to metabolise fibre components in the food that are difficult to digest to short-chain fatty acids such as acetate, propionate and butyrate. They serve as the main source of energy for the enterocytes in the colon and are essential for the maintenance of the muscosal barrier. Regarding their diet, dogs are omnivores. Their digestive system and metabolism are therefore adapted to a high carbohydrate content in their food. This is why a shift in the intestinal flora towards proteolytic bacteria (e.g. <em>Clostridia</em>, <em>Proteus</em>, <em>Klebsiella</em>) and with reduced numbers of saccharolytic bacteria is not a physiological state but a sign of intestinal dysbiosis.</p>
<h2>… and in cats</h2>
<p>Although the anatomical similarities of the gastrointestinal tract suggest otherwise, the composition of the intestinal microbiota is very different in dogs and cats. Figure 2b shows a comparison of the intestinal microbiome of clinically healthy dogs and cats. There is a significant underrepresentation of saccharolytic intestinal microorganisms in cats (<em>E. coli</em>, <em>Fusobacterium spp.</em>, <em>Turicibacter spp.</em>). As in dogs, the reason for this is probably the diet. Domesticated cats are obligatory carnivores and need protein-rich animal tissue to meet their energy needs.</p>
<p>Therefore, their digestive system and metabolism are adapted to a higher protein and lower carbohydrate content in the food. The resulting nutrient supply in the intestine is an enormous selective advantage for proteolytic bacteria and a disadvantage for saccharolytic ones. A eubiotic status of the microbiome in a healthy feline gut is thus characterised by a lower number of saccharolytic and a higher amount of proteolytic bacteria.</p>
<h2>Disorders of the intestinal flora in cats</h2>
<p>Just as in dogs, there are also measurable differences in the composition of the intestinal microbiome between clinically healthy cats and animals with chronic diarrhoea. A comparison of the microbial dysbiosis markers of the two groups shows that the number of saccharolytic intestinal bacteria is significantly increased in cats with chronic diarrhoea compared to clinically healthy animals. This could mean that cats depend less than dogs on microbial fermentation products of saccharolytic bacteria. A shift in the bacterial balance towards saccharolytic intestinal bacteria is therefore more characteristic of a dysbiotic situation in the intestine.</p>
<h2>Similarities and differences</h2>
<p>Despite the differences between dogs and cats regarding their diet and intestinal microbiota, there seem to be certain intestinal bacteria in both species that are essential for maintaining intestinal homeostasis. An example of this is <em>Faecalibacterium prausnitzii</em>. This is a strictly anaerobic gram-positive bacterium with important anti-inflammatory and protective effects on the intestinal mucosa. Reduced copy numbers of this intestinal bacterium are a clear indication of intestinal dysbiosis in dogs and cats.</p>
<p>The opposite seems to be true for bacteria of the species <em>Fusobacterium</em>. In dogs, viable counts of <em>Fusobacterium spp.</em> are significantly higher in the clinically healthy control group than in animals with chronic diarrhoea; in cats, in contrast, this is only true in the affected group (Fig. 2b). It is not clear whether these are different bacterial counts of the same species or of different bacterial species. The environmental conditions in the dysbiotic cat gut may possibly promote the growth of fusobacteria with pro-inflammatory potential, which could favour the occurrence of clinical symptoms.</p>
<h2>Indications to test for dysbiosis</h2>
<p>Even though there are significant differences in the gastrointestinal tract between dogs and cats, the indications for a micro-ecological analysis of the intestinal microbiome are identical in both species. They include:</p>
<ul>
<li>gastrointestinal disorders of unknown origin, e.g. chronic diarrhoea and flatulence</li>
<li>digestive disorders, exocrine pancreatic insufficiency</li>
<li>recurrent parasitoses (e.g. Giardia)</li>
<li>food intolerances and allergies</li>
<li>status monitoring after antibiotic treatment</li>
</ul>
<p>A micro-ecological analysis of the intestinal flora can support the differential diagnosis and provide valuable new therapeutic approaches. However, only microbiological-cultural methods are often used for such tests, for example when determining the bacterial counts of enterococci, bifidobacteria or lactobacilli. For several reasons, these tests are not sufficiently suitable for a diagnosis. On the one hand, with less than 1%, only a very small proportion of the intestinal bacteria is detected. And on the other hand, when comparing the copy numbers of these bacteria in both dogs and cats, there are no significant differences (Fig. 4). This is also true when comparing clinically healthy animals and animals with chronic diarrhoea.</p>
<p>The microbiologically-based, culture- independent analysis of dysbiosis, in contrast, tests and quantifies essential, non-culturable bacterial markers for intestinal dysbacteria. If reference values are adapted, which consider the differences between the normal flora of dogs and cats, intestinal dysbioses can be detected quickly and reliably.</p>
<h2>Treatment of intestinal dysbiosis</h2>
<p>Changing to low-fat, highly digestible food while  taking into account the individual nutritional requirements is the most important step in the treatment of disorders of the intestinal flora. The risk of inflammatory responses and intolerance reactions can be reduced by avoiding raw food and allergen-rich food ingredients. In case of acute diarrhoea, faeces-forming, toxin-binding substances such as aluminosilicate clays or humic acids can effectively relieve the symptoms.</p>
<p>Ground psyllium husks added to the food have a prebiotic effect and promote the growth of the protective flora in a natural way. Additionally, in combination with water, they release mucilage that slows down the intestinal transit in case of diarrhoea and facilitates defaecation in case of constipation.</p>
<p>Only when the acute symptoms have subsided, the use of microbiological therapeutics is indicated. Attention should be paid to always use probiotics in a suitable dosage form (enteric-coated capsules or tablets, microencapsulated powder), high bacterial counts (&gt; 10<sup>9</sup> CFU per dose) and with a high diversity of bacterial species involved.</p>
<p>For all gastrointestinal disorders associated with chronic diarrhoea, oral immunotherapy with autovaccines is also a suitable therapeutic option. Through the increased production of specific antibodies and a supplementary supply of mucosa-nutritive metabolites, the mucosal barrier is supported and the immune defence is strengthened. Its use is recommended both in acute condition and as a cure to prevent recurrence.</p>

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			<h5 class="bodytext"><strong>Literatur</strong></h5>
<ul>
<li class="bodytext">
<h6><span style="color: #808080;"><strong>MK AlShawaqfeh, B Wajid et al.: A dysbiosis index to assess microbial changes in fecal samples of dogs with chronic inflammatory enteropathy. FEMS Microbiology Ecology 2017;11:136</strong></span></h6>
</li>
<li class="bodytext">
<h6><span style="color: #808080;"><strong>L Coelho, J Kultima et al.: Similarity of the dog and human gut microbiomes in gene content and response to diet. Microbiome 2018; volume 6, 72</strong></span></h6>
</li>
</ul>

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