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Peer-reviewed veterinary case report

Muscle weakness and wasting in young adult Great Danes explained

By Chang, Kin-Chow et al.·Published in Veterinary journal (London, England : 1997)·2010·School of Veterinary Medicine and Science, United Kingdom·View original on PubMed

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Original publication title: Molecular and cellular insights into a distinct myopathy of Great Dane dogs.

Species:
dog
Movement & jointsDogs

Plain-English summary

A young adult Great Dane was reported to have progressive weakness and muscle wasting. Researchers studied the dog's muscle tissue and found signs of damage, including changes in muscle structure and an unusual buildup of certain cell components. The affected muscles showed a shift in gene expression that might be the body's way of coping with ongoing muscle damage. This condition is different from similar muscle diseases seen in humans. Unfortunately, the abstract does not provide information on treatment or recovery outcomes for the affected dogs.

People also search for: Great Dane muscle weakness · dog myopathy symptoms · treatment for dog muscle atrophy

Abstract

A myopathy in the Great Dane dog with characteristic pathological and molecular features is reported. Young adults present with progressive weakness and generalised muscle atrophy. To better define this condition, an investigation using histopathology, confocal microscopy, biochemistry and microarray analysis was undertaken. The skeletal muscles of affected dogs exhibited increased oxidative fibre phenotype and core fibre lesions characterised by the disruption of the sarcomeric architecture and the accumulation of mitochondrial organelles. Affected muscles displayed co-ordinated expression of genes consistent with a slow-oxidative phenotype, which was possibly a compensatory response to chronic muscle damage. There was disruption of Z-lines in affected muscles which, at the molecular level, manifested as transcriptional dysregulation of several Z-line associated genes, including alpha-actinin, myotilin, desmin, vimentin and telethonin. The pathology of this canine myopathy is distinct from that of human central core myopathies that are characterised by cores devoid of mitochondria and by the presence of myofibrillar breakdown products.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/19135395/