Acosta-Martínez Maricedes, Gonzalez-Flores Oscar, Etgen Anne M
Department of Neuroscience F113, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Horm Behav. 2006 Apr;49(4):458-62. doi: 10.1016/j.yhbeh.2005.10.002. Epub 2005 Nov 9.
The present study investigated the role of the progestin receptor (PR) and the mitogen-activated protein kinase (MAPK) pathway in the facilitation of lordosis behavior by the delta opioid receptor agonist [D-Pen(2), D-Pen(5)]-enkephalin (DPDPE). Ovariectomized, estrogen-primed rats were treated with the PR antagonist RU486 or the MAPK inhibitor PD98059 prior to intraventricular (icv) infusion of DPDPE. Both RU486 and PD98059 blocked receptive and proceptive behaviors induced by DPDPE at 60 min, and RU486 continued to inhibit estrous behavior at 90 min. Because delta opioid receptors can activate the p42/44 MAPKs, extracellular signal regulated kinases (ERK), we determined the effects of DPDPE on ERK phosphorylation. Icv infusion of DPDPE increased the levels of phosphorylated ERK in the hypothalamus and preoptic area of female rats, assessed by immunoblotting. These results support the participation of the PR and the MAPK pathway in the facilitation of lordosis behavior by delta opioid receptors.
本研究调查了孕激素受体(PR)和丝裂原活化蛋白激酶(MAPK)通路在δ阿片受体激动剂[D-青霉胺(2),D-青霉胺(5)]-脑啡肽(DPDPE)促进脊柱前凸行为中的作用。对去卵巢并用雌激素预处理的大鼠,在脑室内(icv)注入DPDPE之前,用PR拮抗剂RU486或MAPK抑制剂PD98059进行处理。RU486和PD98059在60分钟时均阻断了DPDPE诱导的接受和主动行为,且RU486在90分钟时仍抑制发情行为。由于δ阿片受体可激活p42/44 MAPKs,即细胞外信号调节激酶(ERK),我们测定了DPDPE对ERK磷酸化的影响。通过免疫印迹评估,icv注入DPDPE可增加雌性大鼠下丘脑和视前区磷酸化ERK的水平。这些结果支持PR和MAPK通路参与δ阿片受体对脊柱前凸行为的促进作用。