Letícia Bühler , Ana Carolina de Moura , Márcia Giovenardi , Vincent Goffin , Alberto A. Rasia-Filho
{"title":"循环雌性大鼠后嗅侧内侧杏仁核性别相关基因表达及催乳素对前凸行为的调节。","authors":"Letícia Bühler , Ana Carolina de Moura , Márcia Giovenardi , Vincent Goffin , Alberto A. Rasia-Filho","doi":"10.1016/j.brainres.2025.149602","DOIUrl":null,"url":null,"abstract":"<div><div>The rat posterodorsal medial amygdala (MePD) is sexually dimorphic, has a high concentration of receptors for gonadal hormones and prolactin (PRL), and modulates reproduction. To unravel genetic and functional data for this relevant node of the social behavior network, we studied the expression of <em>ERα, ERβ, GPER1, Kiss1, Kiss1R, PRGR, PRL, PRLR, EGR1, JAK2, STAT5A,</em> and <em>STAT5B</em> in the MePD of males and females along the estrous cycle using the RT-qPCR technique. We also investigated whether PRL in the MePD would affect the sexual behavior display of proestrus females by microinjecting saline, the PRL receptor antagonist Del1-9-G129R-hPRL (1 µM and 10 µM), or PRL (1 nM) and Del1-9-G129R-hPRL (10 µM) 3 h before the onset of the dark-cycle period. The estrogen-dependent lordosis behavior, indicative of sexual receptivity of proestrus females, was recorded and compared before (control) and after (test) microinjections in these groups. Sex differences were found in the right and left MePD gene expression. <em>ERα</em> and <em>Kiss1R,</em> as well as <em>PRL, Short PRLR</em>, and <em>STAT5B</em> expression is higher in cycling females than males. <em>Kiss1</em> expression is higher in males than females, and <em>GPER1</em> is higher during diestrus than proestrus. Furthermore, Del1-9-G129R-hPRL in the MePD significantly reduced the full display and quotient of lordosis in proestrus females, an effect restored by the co-microinjection of PRL. In conjunction, the expression of studied genes showed specific sex and estrous cycle phase features, and PRL action in the MePD plays an essential role in the display of lordosis during the ovulatory period.</div></div>","PeriodicalId":9083,"journal":{"name":"Brain Research","volume":"1857 ","pages":"Article 149602"},"PeriodicalIF":2.7000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sex-related gene expression in the posterodorsal medial amygdala of cycling female rats along with prolactin modulation of lordosis behavior\",\"authors\":\"Letícia Bühler , Ana Carolina de Moura , Márcia Giovenardi , Vincent Goffin , Alberto A. Rasia-Filho\",\"doi\":\"10.1016/j.brainres.2025.149602\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The rat posterodorsal medial amygdala (MePD) is sexually dimorphic, has a high concentration of receptors for gonadal hormones and prolactin (PRL), and modulates reproduction. To unravel genetic and functional data for this relevant node of the social behavior network, we studied the expression of <em>ERα, ERβ, GPER1, Kiss1, Kiss1R, PRGR, PRL, PRLR, EGR1, JAK2, STAT5A,</em> and <em>STAT5B</em> in the MePD of males and females along the estrous cycle using the RT-qPCR technique. We also investigated whether PRL in the MePD would affect the sexual behavior display of proestrus females by microinjecting saline, the PRL receptor antagonist Del1-9-G129R-hPRL (1 µM and 10 µM), or PRL (1 nM) and Del1-9-G129R-hPRL (10 µM) 3 h before the onset of the dark-cycle period. The estrogen-dependent lordosis behavior, indicative of sexual receptivity of proestrus females, was recorded and compared before (control) and after (test) microinjections in these groups. Sex differences were found in the right and left MePD gene expression. <em>ERα</em> and <em>Kiss1R,</em> as well as <em>PRL, Short PRLR</em>, and <em>STAT5B</em> expression is higher in cycling females than males. <em>Kiss1</em> expression is higher in males than females, and <em>GPER1</em> is higher during diestrus than proestrus. Furthermore, Del1-9-G129R-hPRL in the MePD significantly reduced the full display and quotient of lordosis in proestrus females, an effect restored by the co-microinjection of PRL. 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Sex-related gene expression in the posterodorsal medial amygdala of cycling female rats along with prolactin modulation of lordosis behavior
The rat posterodorsal medial amygdala (MePD) is sexually dimorphic, has a high concentration of receptors for gonadal hormones and prolactin (PRL), and modulates reproduction. To unravel genetic and functional data for this relevant node of the social behavior network, we studied the expression of ERα, ERβ, GPER1, Kiss1, Kiss1R, PRGR, PRL, PRLR, EGR1, JAK2, STAT5A, and STAT5B in the MePD of males and females along the estrous cycle using the RT-qPCR technique. We also investigated whether PRL in the MePD would affect the sexual behavior display of proestrus females by microinjecting saline, the PRL receptor antagonist Del1-9-G129R-hPRL (1 µM and 10 µM), or PRL (1 nM) and Del1-9-G129R-hPRL (10 µM) 3 h before the onset of the dark-cycle period. The estrogen-dependent lordosis behavior, indicative of sexual receptivity of proestrus females, was recorded and compared before (control) and after (test) microinjections in these groups. Sex differences were found in the right and left MePD gene expression. ERα and Kiss1R, as well as PRL, Short PRLR, and STAT5B expression is higher in cycling females than males. Kiss1 expression is higher in males than females, and GPER1 is higher during diestrus than proestrus. Furthermore, Del1-9-G129R-hPRL in the MePD significantly reduced the full display and quotient of lordosis in proestrus females, an effect restored by the co-microinjection of PRL. In conjunction, the expression of studied genes showed specific sex and estrous cycle phase features, and PRL action in the MePD plays an essential role in the display of lordosis during the ovulatory period.
期刊介绍:
An international multidisciplinary journal devoted to fundamental research in the brain sciences.
Brain Research publishes papers reporting interdisciplinary investigations of nervous system structure and function that are of general interest to the international community of neuroscientists. As is evident from the journals name, its scope is broad, ranging from cellular and molecular studies through systems neuroscience, cognition and disease. Invited reviews are also published; suggestions for and inquiries about potential reviews are welcomed.
With the appearance of the final issue of the 2011 subscription, Vol. 67/1-2 (24 June 2011), Brain Research Reviews has ceased publication as a distinct journal separate from Brain Research. Review articles accepted for Brain Research are now published in that journal.