Thomas J A, Edwards W D, Felice P R
Endocrinol Exp. 1981 Sep;15(3):171-9.
Cyproterone acetate (CA0 (10 or 20 mg kg-1 daily for 5 days) injected into castrate rats supplemented with testosterone propionate (TP) caused a significant decrease in ventral prostate weights in situ; no inhibitory effects were noted in transplant weights. CA failed to significantly inhibit DNA in either the in situ prostate or transplant, but his anti-androgen caused a significant decrease in the formation of 3H-dihydrotestosterone and 3H-androstanediol from radioactive testosterone in the in situ organ. Histologically, CA caused a decrease in epithelial cell secretory activity.
将醋酸环丙孕酮(CA0,每日10或20毫克/千克,连续5天)注射到补充丙酸睾酮(TP)的去势大鼠体内,可使原位腹侧前列腺重量显著降低;对移植前列腺重量未观察到抑制作用。CA未能显著抑制原位前列腺或移植前列腺中的DNA,但这种抗雄激素药物可使原位器官中放射性睾酮生成3H-双氢睾酮和3H-雄烷二醇的量显著减少。组织学检查显示,CA可导致上皮细胞分泌活性降低。