McArdle's disease with non-insulin-dependent diabetes mellitus: The beneficial effects of hyperglycemia and hyperinsulinemia for exercise intolerance

Internal Medicine

Volumn 35, Issue 5, 1996, Pages 403-406

  Yamauchi, Akira ^a   Amano, Koichi ^a   Ichikawa, Yoichi ^a   Nakamoto, Shinya ^a   Takei, Izumi ^a   Maruyama, Hiroshi ^a   Kono, Norio ^b   Saruta, Takao ^a  

^a KEIO UNIVERSITY   (Japan)

^b OSAKA UNIVERSITY   (Japan)

Author keywords

Forearm ischemic exercise test (FIET); Lactic acid; Muscle phosphorylase

Indexed keywords

CREATINE KINASE; LACTIC ACID; MUSCLE PROTEIN; PHOSPHORYLASE;

ARTICLE; BIOPSY; BLOOD; BRAIN INFARCTION; CASE REPORT; DIET RESTRICTION; EATING; EXERCISE; EXERCISE TEST; FEMALE; GLUCOSE BLOOD LEVEL; GLYCOGEN STORAGE DISEASE TYPE 5; GLYCOLYSIS; HUMAN; HYPERGLYCEMIA; HYPERINSULINISM; METABOLISM; MIDDLE AGED; MUSCLE CRAMP; NON INSULIN DEPENDENT DIABETES MELLITUS; PATHOLOGY; PATHOPHYSIOLOGY; SKELETAL MUSCLE;

BIOPSY; BLOOD GLUCOSE; CEREBRAL INFARCTION; CREATINE KINASE; DIABETES MELLITUS, TYPE 2; EATING; EXERCISE TEST; EXERTION; FASTING; FEMALE; GLYCOGEN STORAGE DISEASE TYPE V; GLYCOLYSIS; HUMANS; HYPERGLYCEMIA; HYPERINSULINISM; LACTIC ACID; MIDDLE AGED; MUSCLE CRAMP; MUSCLE PROTEINS; MUSCLE, SKELETAL; PHOSPHORYLASES;

EID: 0030139950     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.35.403     Document Type: Article

References (15)

1. Layzer RB. McArdle's disease in the 1980's. N Engl J Med 312: 370, 1985 (editorial).
2. Peason CM, Rimer DG, Mommaerts WFHM. A metabolic myopathy due to absence of muscle phosphorylase. Am J Med 30: 502, 1961.
3. Kono N, Mineo I, Sumi S, et al. Metabolic basis of improved exercise tolerance: Muscle phosphorylase deficiency after glucagon administration. Neurology 34: 1471, 1984.
4. McArdle B. Myopathy due to a defect in muscle glycogen breakdown. Clin Sci 10: 13, 1951.
5. Schmid R, Mahler R. Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle. J Clin Invest 38: 2044, 1959.
6. Mommaerts WFHM, Illingworth B, Peason CM, Guillor RJ, Seraydarian K. A functional disorder of muscle associated with the absence of phosphorylase. Proc Natl Acad Sci USA 45: 791, 1959.
7. Braakhekke JP, de Bruin MI, Stegeman DF, Wevers RA, Binkhorst RA, Joosten EMG. The second wind phenomenon in McArdle's disease. Brain 109: 1087, 1986.
8. Schmid R, Hammaker L. Hereditery absence of muscle phosphorylase (McArdle's syndrome). N Engl J Med 264: 223, 1961.
9. Rowland LP, Fahn S, Schotland DL. McArdle's disease: hereditary myopathy due to absence of muscle phosphorylase. Arch Neurol 9: 325, 1963.
10. Viskoper RJ, Wolf E, Chaco J, Katz R, Chowers I. McArdle's syndrome: the relation to a fat-rich diet. Am J Med Sci 269: 217, 1975.
11. Mineo I, Kono N, Shimizu T, Sumi S, Nonaka K, Tarui S. A comparative study on glucagon effect between McArdle's disease and Tarui 's disease. Muscle Nerve 7: 552, 1984.
12. Mineo I, Kono N, Yamada Y, et al. Glucose infusion abolishes the excessive ATP degradation in working muscles of a patient with McArdle's disease. Muscle Nerve 13: 618, 1990.
13. Watanabe M, Matsubara E, Amari M, Okamoto K, Hirai S. McArdle's disease without typical symptoms. Risho Shinkeigaku 30: 1247, 1990.
14. Harris RA, Dowben RM. McArdle's disease in an elderly woman. South Med J 78: 191, 1985.
15. Davies TJ, Harrop JS, Smith JM, Marks V. Neuropathy in a patient with McArdle's syndrome and diabetes mellitus. Horm Metab Res 9: 351, 1977.