Steroid-induced alterations in mRNA expression of the long form of the prolactin receptor in the medial preoptic area of female rats: Effects of exposure to a pregnancy-like regimen of progesterone and estradiol

Robert S. Bridges, Linda E. Hays
{"title":"Steroid-induced alterations in mRNA expression of the long form of the prolactin receptor in the medial preoptic area of female rats: Effects of exposure to a pregnancy-like regimen of progesterone and estradiol","authors":"Robert S. Bridges,&nbsp;Linda E. Hays","doi":"10.1016/j.molbrainres.2005.06.011","DOIUrl":null,"url":null,"abstract":"<div><p><span>It is firmly established that the onset of maternal behavior in the female rat is stimulated by a combination of hormones that include prolactin (PRL), estradiol (E</span><sub>2</sub><span>), and progesterone (P</span><sub>4</sub>). Specifically, nulliparous rats display short latencies to respond to foster young when primed with Silastic capsules filled with P<sub>4</sub> and E<sub>2</sub><span> and then administered PRL centrally to the medial preoptic area (MPOA), an area integrally involved in the expression of maternal behavior in this species. PRL or P</span><sub>4</sub><span> treatments alone are ineffective in stimulating the expression of maternal care. Since the actions of PRL in the MPOA appear to be mediated by PRL receptors, it was of interest to determine whether and how treatment with P</span><sub>4</sub> and E<sub>2</sub> together or separately might alter mRNA expression of the long form of the PRL receptor (PRL-R<sub>L</sub><span><span>) in the MPOA. Using in situ hybridization </span>histochemistry (ISHH), mRNA expression of the PRL-R</span><sub>L</sub> was measured in the MPOA of ovariectomized, nulliparous rats treated with various combinations of P<sub>4</sub> and E<sub>2</sub>. Treatment of animals with P<sub>4</sub> alone for 10 days or with P<sub>4</sub> followed by E<sub>2</sub> for 1 or 4 days resulted in reductions in PRL receptor mRNA expression in the MPOA when compared with the expression in animals treated with E<sub>2</sub> alone or blank capsules. The actions of P<sub>4</sub> on mRNA expression of the PRL-R<sub>L</sub> were more pronounced in the dorsal MPOA. Circulating PRL levels collected at the time of sacrifice were elevated in all groups treated with E<sub>2</sub>, but no association between PRL levels and receptor mRNA expression within the MPOA was evident. These findings indicate that the dorsal MPOA may be one site of progesterone's action in facilitating prolactin-mediated maternal behavior.</p></div>","PeriodicalId":100932,"journal":{"name":"Molecular Brain Research","volume":"140 1","pages":"Pages 10-16"},"PeriodicalIF":0.0000,"publicationDate":"2005-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.molbrainres.2005.06.011","citationCount":"27","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Brain Research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169328X05002640","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 27

Abstract

It is firmly established that the onset of maternal behavior in the female rat is stimulated by a combination of hormones that include prolactin (PRL), estradiol (E2), and progesterone (P4). Specifically, nulliparous rats display short latencies to respond to foster young when primed with Silastic capsules filled with P4 and E2 and then administered PRL centrally to the medial preoptic area (MPOA), an area integrally involved in the expression of maternal behavior in this species. PRL or P4 treatments alone are ineffective in stimulating the expression of maternal care. Since the actions of PRL in the MPOA appear to be mediated by PRL receptors, it was of interest to determine whether and how treatment with P4 and E2 together or separately might alter mRNA expression of the long form of the PRL receptor (PRL-RL) in the MPOA. Using in situ hybridization histochemistry (ISHH), mRNA expression of the PRL-RL was measured in the MPOA of ovariectomized, nulliparous rats treated with various combinations of P4 and E2. Treatment of animals with P4 alone for 10 days or with P4 followed by E2 for 1 or 4 days resulted in reductions in PRL receptor mRNA expression in the MPOA when compared with the expression in animals treated with E2 alone or blank capsules. The actions of P4 on mRNA expression of the PRL-RL were more pronounced in the dorsal MPOA. Circulating PRL levels collected at the time of sacrifice were elevated in all groups treated with E2, but no association between PRL levels and receptor mRNA expression within the MPOA was evident. These findings indicate that the dorsal MPOA may be one site of progesterone's action in facilitating prolactin-mediated maternal behavior.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
类固醇诱导的雌性大鼠内侧视前区长形催乳素受体mRNA表达的改变:暴露于孕激素和雌二醇的影响
已经确定,雌性大鼠的母性行为是由包括催乳素(PRL)、雌二醇(E2)和黄体酮(P4)在内的激素组合刺激的。具体来说,未生育大鼠在注入P4和E2填充的硅胶胶囊,然后将PRL集中注射到内侧视前区(MPOA)时,对培养幼崽的反应潜伏期较短,该区域与该物种的母性行为表达有关。单独使用PRL或P4治疗对刺激母性关怀表达无效。由于PRL在MPOA中的作用似乎是由PRL受体介导的,因此确定P4和E2一起或单独治疗是否以及如何改变MPOA中PRL长链受体(PRL- rl)的mRNA表达是一项有趣的研究。采用原位杂交组织化学(ISHH)方法,测定P4和E2不同组合处理的去卵巢、未生育大鼠MPOA中PRL-RL mRNA的表达。与单独使用E2或空白胶囊的动物相比,单独使用P4治疗10天或P4后再使用E2治疗1天或4天的动物,MPOA中PRL受体mRNA的表达减少。P4对MPOA背侧PRL-RL mRNA表达的影响更为明显。E2处理组在牺牲时收集的循环PRL水平均升高,但PRL水平与MPOA内受体mRNA表达之间无明显关联。这些发现表明,背侧MPOA可能是孕酮促进催乳素介导的母性行为的一个部位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Editorial Board Author Index Co-expression of the 5-HT3B subunit with the 5-HT3A receptor reduces alcohol sensitivity Genes required for fructose metabolism are expressed in Purkinje cells in the cerebellum Tolloid-like 1 is negatively regulated by stress and glucocorticoids
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1