Changes in pituitary gonadotropin subunits and hypothalamic Kiss-1 gene expression by administration of sex steroids in ovary-intact female rats
Objective We examined how the sex steroids influence the synthesis of gonadotropins. Materials and Methods The effects of sex steroids estradiol (E2), progesterone (P4), and dihydrotestosterone (DHT) in pituitary gonadotroph cell model (LβT2 cells) in vitro and ovary-intact rats in vivo were examine...
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Published in | Endocrine Vol. 83; no. 3; pp. 733 - 746 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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01.03.2024
Springer Nature B.V |
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Abstract | Objective
We examined how the sex steroids influence the synthesis of gonadotropins.
Materials and Methods
The effects of sex steroids estradiol (E2), progesterone (P4), and dihydrotestosterone (DHT) in pituitary gonadotroph cell model (LβT2 cells) in vitro and ovary-intact rats in vivo were examined. The effects of sex steroids on Kiss1 gene expression in the hypothalamus were also examined in ovary-intact rats.
Results
In LβT2 cells, E2 increased common glycoprotein alpha (Cga) and luteinizing hormone beta (Lhb) subunit promoter activity as well as their mRNA expression. Although gonadotropin subunit promoter activity was not modulated by P4, Cga and Lhb mRNA expression was increased by P4. DHT inhibited Cga and Lhb mRNA expression with a concomitant decrease in their promoter activity. During the 2-week administration of exogenous E2 to ovary-intact rats, the estrous cycle determined by vaginal smears was disrupted. P4 or DHT administration completely eliminated the estrous cycle. Protein expression of all three gonadotropin subunits within the pituitary gland was inhibited by E2 or P4 treatment in vivo; however, DHT reduced Cga expression but did not modulate Lhb or follicle-stimulating hormone beta subunit expression. E2 administration significantly repressed Kiss1 mRNA expression in a posterior hypothalamic region that included the arcuate nucleus. P4 and DHT did not modulate Kiss1 mRNA expression in this region. In contrast, P4 administration significantly inhibited Kiss1 mRNA expression in the anterior region of the hypothalamus that included the anteroventral periventricular nucleus. The expression of gonadotropin-releasing hormone (Gnrh) mRNA in the anterior hypothalamic region, where the preoptic area is located, appeared to be decreased by treatment with E2 and P4.
Conclusion
Our findings suggest that sex steroids have different effects in the hypothalamus and pituitary gland. |
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AbstractList | OBJECTIVEWe examined how the sex steroids influence the synthesis of gonadotropins.MATERIALS AND METHODSThe effects of sex steroids estradiol (E2), progesterone (P4), and dihydrotestosterone (DHT) in pituitary gonadotroph cell model (LβT2 cells) in vitro and ovary-intact rats in vivo were examined. The effects of sex steroids on Kiss1 gene expression in the hypothalamus were also examined in ovary-intact rats.RESULTSIn LβT2 cells, E2 increased common glycoprotein alpha (Cga) and luteinizing hormone beta (Lhb) subunit promoter activity as well as their mRNA expression. Although gonadotropin subunit promoter activity was not modulated by P4, Cga and Lhb mRNA expression was increased by P4. DHT inhibited Cga and Lhb mRNA expression with a concomitant decrease in their promoter activity. During the 2-week administration of exogenous E2 to ovary-intact rats, the estrous cycle determined by vaginal smears was disrupted. P4 or DHT administration completely eliminated the estrous cycle. Protein expression of all three gonadotropin subunits within the pituitary gland was inhibited by E2 or P4 treatment in vivo; however, DHT reduced Cga expression but did not modulate Lhb or follicle-stimulating hormone beta subunit expression. E2 administration significantly repressed Kiss1 mRNA expression in a posterior hypothalamic region that included the arcuate nucleus. P4 and DHT did not modulate Kiss1 mRNA expression in this region. In contrast, P4 administration significantly inhibited Kiss1 mRNA expression in the anterior region of the hypothalamus that included the anteroventral periventricular nucleus. The expression of gonadotropin-releasing hormone (Gnrh) mRNA in the anterior hypothalamic region, where the preoptic area is located, appeared to be decreased by treatment with E2 and P4.CONCLUSIONOur findings suggest that sex steroids have different effects in the hypothalamus and pituitary gland. We examined how the sex steroids influence the synthesis of gonadotropins. The effects of sex steroids estradiol (E2), progesterone (P4), and dihydrotestosterone (DHT) in pituitary gonadotroph cell model (LβT2 cells) in vitro and ovary-intact rats in vivo were examined. The effects of sex steroids on Kiss1 gene expression in the hypothalamus were also examined in ovary-intact rats. In LβT2 cells, E2 increased common glycoprotein alpha (Cga) and luteinizing hormone beta (Lhb) subunit promoter activity as well as their mRNA expression. Although gonadotropin subunit promoter activity was not modulated by P4, Cga and Lhb mRNA expression was increased by P4. DHT inhibited Cga and Lhb mRNA expression with a concomitant decrease in their promoter activity. During the 2-week administration of exogenous E2 to ovary-intact rats, the estrous cycle determined by vaginal smears was disrupted. P4 or DHT administration completely eliminated the estrous cycle. Protein expression of all three gonadotropin subunits within the pituitary gland was inhibited by E2 or P4 treatment in vivo; however, DHT reduced Cga expression but did not modulate Lhb or follicle-stimulating hormone beta subunit expression. E2 administration significantly repressed Kiss1 mRNA expression in a posterior hypothalamic region that included the arcuate nucleus. P4 and DHT did not modulate Kiss1 mRNA expression in this region. In contrast, P4 administration significantly inhibited Kiss1 mRNA expression in the anterior region of the hypothalamus that included the anteroventral periventricular nucleus. The expression of gonadotropin-releasing hormone (Gnrh) mRNA in the anterior hypothalamic region, where the preoptic area is located, appeared to be decreased by treatment with E2 and P4. Our findings suggest that sex steroids have different effects in the hypothalamus and pituitary gland. Objective We examined how the sex steroids influence the synthesis of gonadotropins. Materials and Methods The effects of sex steroids estradiol (E2), progesterone (P4), and dihydrotestosterone (DHT) in pituitary gonadotroph cell model (LβT2 cells) in vitro and ovary-intact rats in vivo were examined. The effects of sex steroids on Kiss1 gene expression in the hypothalamus were also examined in ovary-intact rats. Results In LβT2 cells, E2 increased common glycoprotein alpha (Cga) and luteinizing hormone beta (Lhb) subunit promoter activity as well as their mRNA expression. Although gonadotropin subunit promoter activity was not modulated by P4, Cga and Lhb mRNA expression was increased by P4. DHT inhibited Cga and Lhb mRNA expression with a concomitant decrease in their promoter activity. During the 2-week administration of exogenous E2 to ovary-intact rats, the estrous cycle determined by vaginal smears was disrupted. P4 or DHT administration completely eliminated the estrous cycle. Protein expression of all three gonadotropin subunits within the pituitary gland was inhibited by E2 or P4 treatment in vivo; however, DHT reduced Cga expression but did not modulate Lhb or follicle-stimulating hormone beta subunit expression. E2 administration significantly repressed Kiss1 mRNA expression in a posterior hypothalamic region that included the arcuate nucleus. P4 and DHT did not modulate Kiss1 mRNA expression in this region. In contrast, P4 administration significantly inhibited Kiss1 mRNA expression in the anterior region of the hypothalamus that included the anteroventral periventricular nucleus. The expression of gonadotropin-releasing hormone (Gnrh) mRNA in the anterior hypothalamic region, where the preoptic area is located, appeared to be decreased by treatment with E2 and P4. Conclusion Our findings suggest that sex steroids have different effects in the hypothalamus and pituitary gland. |
Author | Yacca, Susdiaman S. Oride, Aki Tumurbaatar, Tuvshintugs Kyo, Satoru Kanasaki, Haruhiko Cairang, Zhuoma Okada, Hiroe |
Author_xml | – sequence: 1 givenname: Susdiaman S. surname: Yacca fullname: Yacca, Susdiaman S. organization: Department of Obstetrics and Gynecology, Shimane University School of Medicine – sequence: 2 givenname: Haruhiko surname: Kanasaki fullname: Kanasaki, Haruhiko email: kanasaki@med.shimane-u.ac.jp organization: Department of Obstetrics and Gynecology, Shimane University School of Medicine – sequence: 3 givenname: Tuvshintugs surname: Tumurbaatar fullname: Tumurbaatar, Tuvshintugs organization: Department of Obstetrics and Gynecology, Shimane University School of Medicine – sequence: 4 givenname: Zhuoma surname: Cairang fullname: Cairang, Zhuoma organization: Department of Obstetrics and Gynecology, Shimane University School of Medicine – sequence: 5 givenname: Aki surname: Oride fullname: Oride, Aki organization: Department of Obstetrics and Gynecology, Shimane University School of Medicine – sequence: 6 givenname: Hiroe surname: Okada fullname: Okada, Hiroe organization: Department of Obstetrics and Gynecology, Shimane University School of Medicine – sequence: 7 givenname: Satoru surname: Kyo fullname: Kyo, Satoru organization: Department of Obstetrics and Gynecology, Shimane University School of Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37966704$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1111/j.1365-2826.2008.01708.x 10.3389/fendo.2022.925206 10.1210/en.2005-0323 10.1677/jme.1.01755 10.1210/me.2003-0115 10.1016/j.fertnstert.2010.03.034 10.1210/mend-3-3-474 10.1371/journal.pone.0280238 10.1093/humupd/dmu009 10.1016/j.ygcen.2017.01.014 10.1677/joe.1.06508 10.1210/jcem-58-2-378 10.1210/jcem-73-3-621 10.1210/endo-109-5-1414 10.1093/biolre/iox030 10.1073/pnas.92.26.12280 10.1262/jrd.18146 10.1210/mend-2-7-641 10.1210/en.2006-1435 10.1080/09513590.2017.1318277 10.1210/me.2009-0350 10.1210/en.2011-1904 10.1210/me.2005-0316 10.2144/05391RV01 10.1210/en.2005-0488 10.3389/fendo.2019.00047 10.1210/edrv-11-1-177 10.1111/j.1365-2826.2009.01835.x 10.1177/1087057110369701 10.1095/biolreprod.103.019588 |
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Keywords | Kisspeptin Gonadotropins Hypothalamus Sex steroids Pituitary |
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We examined how the sex steroids influence the synthesis of gonadotropins.
Materials and Methods
The effects of sex steroids estradiol (E2),... We examined how the sex steroids influence the synthesis of gonadotropins. The effects of sex steroids estradiol (E2), progesterone (P4), and... ObjectiveWe examined how the sex steroids influence the synthesis of gonadotropins.Materials and MethodsThe effects of sex steroids estradiol (E2),... OBJECTIVEWe examined how the sex steroids influence the synthesis of gonadotropins.MATERIALS AND METHODSThe effects of sex steroids estradiol (E2),... |
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SubjectTerms | 17β-Estradiol Arcuate nucleus Diabetes Dihydrotestosterone Endocrinology Estrus cycle Follicle-stimulating hormone Gene expression Gonadotropin-releasing hormone Gonadotropins Humanities and Social Sciences Hypothalamus Hypothalamus (anterior) Internal Medicine Kiss1 protein Luteinizing hormone Medicine Medicine & Public Health multidisciplinary Original Article Ovaries Periventricular nucleus Pituitary Pituitary (anterior) Pituitary gland Preoptic area Progesterone Science Steroid hormones Steroids |
Title | Changes in pituitary gonadotropin subunits and hypothalamic Kiss-1 gene expression by administration of sex steroids in ovary-intact female rats |
URI | https://link.springer.com/article/10.1007/s12020-023-03596-0 https://www.ncbi.nlm.nih.gov/pubmed/37966704 https://www.proquest.com/docview/2933033267 https://search.proquest.com/docview/2890360861 |
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