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纳曲酮对大鼠性接受能力的促进作用。

Naltrexone facilitation of sexual receptivity in the rat.

作者信息

Allen D L, Renner K J, Luine V N

出版信息

Horm Behav. 1985 Mar;19(1):98-103. doi: 10.1016/0018-506x(85)90010-8.

Abstract

Naltrexone hydrochloride (3mg/kg) facilitated sexual receptivity in ovariectomized female rats given estradiol benzoate 44 hr previously. The latency of naltrexone facilitation is 3 hr, which is similar to that by progesterone. Other doses of naltrexone (1 and 5 mg/kg) were ineffective. Unlike the effect of progesterone, the facilitation of behavior by naltrexone is not blocked by the protein synthesis inhibitor anisomycin. Naltrexone facilitation was blocked by pargyline, a monoamine oxidase inhibitor.

摘要

盐酸纳曲酮(3毫克/千克)可促进在44小时前已给予苯甲酸雌二醇的去卵巢雌性大鼠的性接受能力。纳曲酮促进作用的潜伏期为3小时,这与孕酮的作用潜伏期相似。其他剂量的纳曲酮(1毫克/千克和5毫克/千克)无效。与孕酮的作用不同,纳曲酮对行为的促进作用不会被蛋白质合成抑制剂茴香霉素阻断。纳曲酮的促进作用被单胺氧化酶抑制剂帕吉林阻断。

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