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Azoturia, new thoughts on an old conditionAzoturia is a problem that affects the muscles of many horses. The signs associated with the condition range from stiffness and mild cramp to the horse becoming unable to move at all. Other terms that have been used for the problem are Monday Morning Disease, Tying-Up, Myositis and Setfast. It is unlikely that a single process can explain all the clinical types, but the term Equine Rhabdomyolysis Syndrome is probably the most accurate description. Azoturia can affect any horse of any age but is much more common in fillies
and mares than geldings and stallions. This condition affects all breeds
and sizes of horses and is traditionally seen in animals that have been
exercised following a period of rest without a reduction in feed intake,
hence the old name called Monday morning disease as most work
horses were never exercised on a Sunday. It is particularly seen in horse
on a high carbohydrate diet (in particular horses feed straights (barley
and oats). The signs develop particularly at the end of strenuous
exercise and the horse may pull itself up or the rider becomes aware that
the horse is reluctant to go forward. Forcing the horse to move
only exacerbates the problem as it causes further muscle damage. Horses
suffering from azoturia have intense muscle cramps and pain and are reluctant
to move. In extreme cases horses can have such severe muscle tissue
damage that breakdown products from the muscles result in severe (occasionally
irreparable) kidney damage. The products of muscle damage cause
the urine often to have a red tinge. The amount of muscle damage
is usually assessed by a blood sample and the levels of two enzymes (CK
and AST) are an indicator of the amount of damage. The same enzymes
can also be monitored to assess how the muscles are repairing. A mutation in a gene has been highly associated with presence of abnormal polysaccharide in muscle biopsy in several horse breeds. This supports the hereditary nature of the disease, foals from affected parents are more likely to have the condition themselves. There is a genetic test for this mutation which can be obtained from a blood sample from a horse you are suspicious has the disease. A diagnosis of EPSM is confirmed following histopathology of a muscle biopsy from either the semimembranosus or semitendinosus muscles to the side of the tail. Using special stains it is possible to examine the muscle cells and horses with EPSM have very high levels of glycogen and polysaccharides in the affected cells . A laboratory has recently been set up at the University of Edinburgh to investigate equine nerve and muscle problems like EPSM. Providing a high fat, low carbohydrate diet is the most important part
of treatment. There are now proprietary foods available with high fat
concentrations. Selenium and Vitamin E may help reduce the
chance of further attacks due to their anti-oxidant affect although their
usefullness has been over-rated in the past. Grass or legume (alfalfa)
is also a good feed stuff. It is also critical that horses with
EPSM get as much daily turnout and as much regular work as possible. Because
the muscles are loaded with excessive carbohydrates it often take many
months of the high fat diet for the signs to decrease. References
DISCLAIMER The material contained in this website is presented for information purposes only . The material is in no way intended to replace professional veterinary care or attention from a professional veterinary surgeon. The advice given in any of our web pages cannot be used as the basis for a diagnosis or choice of treatment. Clyde Vet Group advises that you should always consult a veterinary surgeon about any queries with animals under your care.
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