González-Flores Oscar, Etgen Anne M
Department of Neuroscience F113, Albert Einstein College of Medicine (AECOM), Bronx, NY 10461, USA.
Horm Behav. 2004 Jan;45(1):50-7. doi: 10.1016/j.yhbeh.2003.08.003.
Intracerebral and intravenous administration of progesterone (P) and its ring A-reduced metabolites induces intense sexual behavior (lordosis and proceptivity) in estrogen-primed rats. The present study tested the hypothesis that the nitric oxide-cGMP-protein kinase G pathway is involved in the facilitation of sexual behavior induced by the intracerebroventricular (i.c.v.) administration of P (130 ng) and its ring A-reduced metabolites 5alpha-dihydroprogesterone (5alpha-DHP; 13 ng) and 5alpha,3alpha-pregnanolone (5alpha,3alpha-Pgl; 13 ng). In Experiment 1, we tested the relevance of the nitric oxide/cGMP pathway by infusing a nitric oxide synthase inhibitor or a nitric oxide-dependent, soluble guanylyl cyclase inhibitor icv before progestin administration. The lordosis induced by P, 5alpha-DHP and 5alpha,3alpha-Pgl was significantly reduced at 2 h after progestin infusion by the previous injection of either a nitric oxide synthase inhibitor or by a soluble guanylyl cyclase inhibitor. Lordosis behavior returned to control values by 4 h. In Experiment 2, i.c.v. infusion of the protein kinase G inhibitor KT5823 significantly inhibited the lordosis behavior induced by all three progestins at 2 h. These data support the hypothesis that the nitric oxide/cGMP/protein kinase G pathway is involved in the lordosis induced by P and some of its ring A-reduced metabolites.
脑内和静脉注射孕酮(P)及其A环还原代谢产物可在雌激素预处理的大鼠中诱导强烈的性行为(脊柱前凸和求偶行为)。本研究检验了以下假设:一氧化氮 - 环鸟苷酸 - 蛋白激酶G途径参与了脑室内(i.c.v.)注射P(130 ng)及其A环还原代谢产物5α - 二氢孕酮(5α - DHP;13 ng)和5α,3α - 孕烷醇酮(5α,3α - Pgl;13 ng)所诱导的性行为促进过程。在实验1中,我们在给予孕激素之前通过脑室内注入一氧化氮合酶抑制剂或一氧化氮依赖性可溶性鸟苷酸环化酶抑制剂来测试一氧化氮/环鸟苷酸途径的相关性。在注入孕激素后2小时,预先注射一氧化氮合酶抑制剂或可溶性鸟苷酸环化酶抑制剂可显著降低P、5α - DHP和5α,3α - Pgl所诱导的脊柱前凸。脊柱前凸行为在4小时后恢复到对照值。在实验2中,脑室内注入蛋白激酶G抑制剂KT5823在2小时时显著抑制了所有三种孕激素所诱导的脊柱前凸行为。这些数据支持了以下假设:一氧化氮/环鸟苷酸/蛋白激酶G途径参与了P及其一些A环还原代谢产物所诱导的脊柱前凸。