INCREASED SERUM ALANINE AMINOTRANSFERASE ACTIVITY ASSOCIATED WITH MUSCLE NECROSIS IN THE DOG

被引:73
作者
VALENTINE, BA
BLUE, JT
SHELLEY, SM
COOPER, BJ
机构
[1] Department of Pathology, New York State College of Veterinary Medicine, Cornell University, Ithaca, New York
关键词
D O I
10.1111/j.1939-1676.1990.tb00886.x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Serum activity of alanine aminotransferase (ALT) was consistently increasedin dogs with canine X‐linked muscular dystrophy (CXMD), a primary myopathy characterized by profound and on‐going skeletal muscle necrosis. In order to determine whether the ALT was of liver origin, serum activity of creatine kinase (CK), aspartate aminotransferase (AST), ALT, and sorbitol dehydrogenase (SDH) obtained from dystrophic dogs was compared with enzyme activity present in clinically normal dogs. In dystrophic dogs at all ages tested, serum activity of CK, AST, and ALT was increased, and significant increases were present in dogs four weeks or older. In contrast, SDH activity in dystrophic dogs was not statistically different from values in clinically normal dogs. Ultrastructural examination of liver tissue revealed no evidence of hepatic degeneration in dystrophic dogs. It was concluded that increased serum activity of ALT in the dog may be associated with severe skeletal muscle degeneration, without concurrent hepatocellular necrosis. (Journal of Veterinary Internal Medicine 1990; 4:140–143) Copyright © 1990, Wiley Blackwell. All rights reserved
引用
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页码:140 / 143
页数:4
相关论文
共 19 条
[1]  
Cooper BJ, Winand NJ, Stedman H., Et al., The homologue of the Duchenne locus is defective in X‐linked muscular dystrophy of dogs, Nature, 334, pp. 154-156, (1988)
[2]  
Hoffman EP, Hudecki MS, Rosenberg PA, Et al., Cell and fibertype distribution of dystrophin, Neuron, 1, pp. 411-420, (1988)
[3]  
Koenig M., Hoffman EP, Bertelson CJ, Et al., Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organizationof theDMD gene in normal and affected individuals, Cell, 50, pp. 509-517, (1987)
[4]  
Zubrzycka-Gaarn EE, Bulman DE, Karpati G., Et al., The Duchenne muscular dystrophy gene product is localized in sarco‐lemma of human skeletal muscle, Nature, 333, pp. 466-469, (1988)
[5]  
Watkins SC, Hoffman EP, Slayter HS, Et al., Immunoelectron microscopic localization of dystrophin in myofibres, Nature, 333, pp. 863-866, (1988)
[6]  
Hunter S., The heart in muscular dystrophy, Br Med Bull, 36, pp. 133-134, (1980)
[7]  
Valentine BA, Cooper BJ, de Lahunta A., Et al., Canine X‐linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: Clinical studies, J Neurol Sci, 88, pp. 69-81, (1988)
[8]  
Bevans M., Changes in the musculature of the gastrointestinal tract and in the myocardium in progressive muscular dystrophy, Arch Pathol Lab Med, 40, pp. 225-238, (1945)
[9]  
Kramer JW., Clinical enzymology, Clinical Biochemistry of Domestic Animals, pp. 175-199, (1980)
[10]  
Boyd JW., The mechanisms relating to increases in plasma enzymes and isoenzymes in diseases of animals, Veterinary Clinical Pathology, 12, pp. 9-24, (1983)