Chen W, Zhou X M, Chen D Y, Kang J S
Department of Urologic Surgery, Nanjing Railway Medical College, People's Republic of China.
Urol Res. 1988;16(5):363-6. doi: 10.1007/BF00256043.
The antiandrogenic potency of cimetidine, progesterone, cannitracin and tolazoline was studied in intact immature rats by determination of the weight and DNA content of the ventral prostate. Cimetidine is a H-2-receptor histamine antagonist, cannitracin is an antifungal antibiotic derived from Strp-griseus and tolazoline is an alpha-adrenergic blocker similar to phentolamine. All rats (except the control group) received testosterone propionate (TP) 0.3 mg s.c. with the drugs above every day for one week. Cimetidine, progesterone and cannitracin, but not tolazoline, significantly decreased the weight and DNA content of the hyperplastic prostate induced by TP. The results indicate that cimetidine, progesterone and cannitracin have an antiandrogenic effect. This study provides the basis for investigating the effects of antiandrogen in men with symptomatic benign prostatic hyperplasia.
通过测定未成熟完整大鼠腹侧前列腺的重量和DNA含量,研究了西咪替丁、孕酮、克念菌素和妥拉唑啉的抗雄激素作用。西咪替丁是一种H-2受体组胺拮抗剂,克念菌素是一种源自灰链霉菌的抗真菌抗生素,妥拉唑啉是一种类似于酚妥拉明的α-肾上腺素能阻滞剂。所有大鼠(对照组除外)每天皮下注射0.3 mg丙酸睾酮(TP),并同时给予上述药物,持续一周。西咪替丁、孕酮和克念菌素可显著降低由TP诱导的增生前列腺的重量和DNA含量,而妥拉唑啉则无此作用。结果表明,西咪替丁、孕酮和克念菌素有抗雄激素作用。本研究为研究抗雄激素对有症状良性前列腺增生男性的影响提供了依据。