Mazzucco Christine A, Walker Hope A, Pawluski Jodi L, Lieblich Stephanie E, Galea Liisa A M
Department of Psychology, University of British Columbia, 2136 West Mall, Vancouver, BC V6T 1Z4, Canada.
Behav Brain Res. 2008 Aug 5;191(1):111-7. doi: 10.1016/j.bbr.2008.03.016. Epub 2008 Mar 21.
Estrogen has well known effects on sexual behavior, however the role of the estrogen receptors (ER) alpha and beta on sexual behavior remains to be fully determined. This study investigated the individual and co-operative involvement of ERalpha and beta on sexual behaviors in the adult female rat. Subtype selective ER agonists, propyl-pyrazole triol (PPT; ERalpha agonist) and diarylpropionitrile (DPN; ERbeta agonist) were utilized to examine each receptor subtype's contribution, individual and co-operative, for both receptive (lordosis) and proceptive (hopping/darting, 'ear wiggling') female sexual behaviors. Ovariectomized female rats received subcutaneous injections of either: sesame oil (OIL), dimethylsulfoxide (DMSO), estradiol benzoate (EB; 10 microg/0.1 ml OIL), one of three doses of the ERalpha agonist PPT (1.25mg, 2.5mg or 5.0mg/0.1 ml DMSO), one of three doses of the ERbeta agonist DPN (1.25mg, 2.5mg or 5.0mg/0.1 ml DMSO) or a combination dose of PPT and DPN (2.5mg PPT+2.5mg DPN/0.1 ml DMSO) for two consecutive days, 48 and 24h prior to testing followed by a progesterone injection (500 microg/0.1 ml OIL) 4h prior to testing in order to elicit sexual behavior. The ERalpha agonist PPT, but not the ERbeta agonist DPN, elicited both proceptive and receptive behavior. PPT at doses of 2.5 and 5.0mg significantly elicited lordosis and proceptive behavior ('ear wiggling', hopping and darting). Intriguingly, the administration of both agonists together at the 2.5mg dose resulted in reduced levels of proceptivity and receptivity, suggesting that ERbeta modulates ERalpha's ability to elicit receptive and proceptive sexual behavior.
雌激素对性行为有众所周知的影响,然而雌激素受体(ER)α和β在性行为中的作用仍有待全面确定。本研究调查了ERα和β在成年雌性大鼠性行为中的单独及协同作用。使用亚型选择性ER激动剂丙基吡唑三醇(PPT;ERα激动剂)和二芳基丙腈(DPN;ERβ激动剂)来检查每种受体亚型对雌性接受性(脊柱前凸)和主动性(跳跃/飞奔、“耳朵摆动”)性行为的单独及协同贡献。去卵巢的雌性大鼠皮下注射以下物质之一:芝麻油(OIL)、二甲基亚砜(DMSO)、苯甲酸雌二醇(EB;10微克/0.1毫升OIL)、三种剂量之一的ERα激动剂PPT(1.25毫克、2.5毫克或5.0毫克/0.1毫升DMSO)、三种剂量之一的ERβ激动剂DPN(1.25毫克、2.5毫克或5.0毫克/0.1毫升DMSO)或PPT和DPN的联合剂量(2.5毫克PPT + 2.5毫克DPN/0.1毫升DMSO),连续两天,在测试前48小时和24小时注射,然后在测试前4小时注射孕酮(500微克/0.1毫升OIL)以引发性行为。ERα激动剂PPT而非ERβ激动剂DPN引发了主动性和接受性行为。2.5毫克和5.0毫克剂量的PPT显著引发了脊柱前凸和主动性行为(“耳朵摆动”、跳跃和飞奔)。有趣的是,两种激动剂以2.5毫克剂量一起给药导致主动性和接受性水平降低,这表明ERβ调节ERα引发接受性和主动性性行为的能力。