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Showing posts with label methylandrostenediol (Methandriol). Show all posts
Showing posts with label methylandrostenediol (Methandriol). Show all posts

Plasma fibrinolytic activity following oral anabolic steroid therapy.

. Monday, 14 July 2008
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Thromb Diath Haemorrh. 1975 Sep 30;34(1):236-45.

Plasma fibrinolytic activity following oral anabolic steroid therapy.

Walker ID, Davidson JF, Young P, Conkie JA.

Six anabolic steroids were assessed for their ability to enhance plasma
fibrinolytic activity in males with ischaemic heart disease. Five
17alpha-alkylated steroids (Ethyloestrenol, Norethandrolone, Methandienone,
Methylandrostenediol and Oxymetholone) were examined and all produced a
significant increase in plasma plasminogen activator as measured by the
euglobulin lysis time. The only non-17alpha-alkylated steroid studied
(Methenolone acetate) failed to enhance fibrinolysis. The 17alpha-alkylated
steroids studied all deserve more detailed evaluation of their long term effects
on plasma fibrinolytic activity.

Androgenic/Anabolic steroid-induced toxic hepatitis.

. Friday, 11 July 2008
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J Clin Gastroenterol. 2002 Oct;35(4):350-2.

Androgenic/Anabolic steroid-induced toxic hepatitis.

Stimac D, Milić S, Dintinjana RD, Kovac D, Ristić S.

Division of Gastroenterology, Department of Internal Medicine, Clinical Hospital
Center Rijeka, Rijeka, Croatia. davor.stimac@ri.hinet.hr

Athletes and bodybuilders often misuse androgenic/anabolic steroids. When used in
therapeutic doses, these drugs produce clinical jaundice in just a small number
of recipients. We present a 26-year-old male bodybuilder who self-administered
high doses of androgenic/anabolic steroids that induced liver damage. One month
before admission to the hospital, he used testosterone enanthate (500 mg
intramuscularly, twice weekly), stanozolol (40 mg/d), and methylandrostenediol
(30 mg/d by mouth, for 5 weeks). On admission, his bilirubin level was 470
micromol/L (direct, 360 micromol/L), his aspartate aminotransferase (AST) level
was 5,870 IU/L, his alanine aminotransferase (ALT) level was 10,580 IU/L, his
alkaline phosphatase (ALP) level was 152 IU/L, his gamma-glutamyl-transpeptidase
level was 140 IU/L, his albumin level was 27.6 g/L, and his prothrombin time was
29%. During the patient's prolonged hospitalization, multiple tests and liver
biopsy were performed, showing only toxic hepatic lesions. The patient was
provided with supportive medical treatment. Clinical signs and laboratory
findings improved substantially 12 weeks after the patient discontinued
androgenic/anabolic steroids. The reasons for presenting this case were the much
higher values of AST and ALT levels than reported in other studies, although the
values of bilirubin and ALP were similar to those found in the literature. To our
knowledge, it is the first case of toxic hepatitis induced by androgenic/anabolic
steroids with predominantly hepatocellular necrosis instead of intrahepatic
cholestasis.