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NEUROLOGY 1974;24:237
© 1974 American Academy of Neurology

Pargyline-induced myopathy with histochemical characteristics of Duchenne muscular dystrophy

MARIO K. YU, M.D., THOMAS L. WRIGHT, B.S., WOLF-D. DETTBARN, M.D. and WILLIAM H. OLSON, M.D.

In Sprague-Dawley rats, daily intraperitoneal injections of pargyline, a monoamine oxidase inhibitor, produces a myopathy with grouped lesions, excess connective tissue, and sarcoplasmic fluorescence by the Falck-Hillarp technique. The myopathy is prevented by prior denervation and appears to be slightly accentuated by prior aortic ligation. A possible mechanism is thought to be an intraneuronal or intrafibrillar, or both, accumulation of catecholamines, resulting in the release of excessive acetylcholine or other substances at the myoneural junction. The experiments support the possibility of a relationship between Duchenne muscular dystrophy and biogenic arnine metabolism by showing that pargyline produces a myopathy with the histopathologic: characteristics of Duchenne muscular dystrophy.

Dr. Olson's address Department of Neurolog, Vanderbilt University School of Medicine, Nashville, TN 37232.

Read at the twenty-fifth annual meeting of the American Academy of Neurology, Boston, Massachusetts, April, 1973.

This study was supported by grants from the Unitcd States Public Health Service (I POINS 10175) and the Muscular Dystrophy Associations of America.

Received for publicatinn June 26, 1973.







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