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https://hdl.handle.net/11499/10500
Title: | The integrated hypothalamic tachykinin-kisspeptin system as a central coordinator for reproduction | Authors: | Navarro, V.M. Bosch, M.A. León, S. Simavli, Serap True, C. Pinilla, L. Carroll, R.S. |
Keywords: | estradiol gonadorelin gonadotropin kisspeptin luteinizing hormone messenger RNA neurokinin 1 receptor neurokinin 2 receptor neurokinin 3 receptor neurokinin A substance P follitropin G protein coupled receptor Kiss1 protein, mouse Kiss1r protein, mouse tachykinin receptor adult animal cell animal experiment animal model animal tissue arcuate nucleus Article controlled study female gonadorelin release gonadotropin release hormonal regulation luteinizing hormone release male mouse nonhuman priority journal protein expression reproduction thalamus ventral nucleus agonists animal C57BL mouse hypothalamus knockout mouse metabolism secretion (process) Animals Estradiol Female Follicle Stimulating Hormone Gonadotropin-Releasing Hormone Hypothalamus Kisspeptins Luteinizing Hormone Male Mice, Inbred C57BL Mice, Knockout Neurokinin A Receptors, G-Protein-Coupled Receptors, Tachykinin Reproduction Substance P |
Publisher: | Endocrine Society | Abstract: | Tachykinins are comprised of the family of related peptides, substance P (SP), neurokinin A (NKA), and neurokinin B (NKB). NKB has emerged as regulator of kisspeptin release in the arcuate nucleus (ARC), whereas the roles of SP and NKA in reproduction remain unknown. This work explores the roles of SP and NKA in the central regulation of GnRH release. First, central infusion of specific agonists for the receptors of SP (neurokinin receptor 1, NK1R), NKA (NK2R) and NKB (NK3R) each induced gonadotropin release in adult male and ovariectomized, estradiol-replaced female mice, which was absent in Kiss1r-/- mice, indicating a kisspeptin-dependent action. The NK2R agonist, however, decreasedLHrelease in ovariectomized-sham replaced females, as documented forNK3R agonists but in contrast to the NK1R agonist, which further increased LH release. Second, Tac1 (encoding SP and NKA) expression in the ARC and ventromedial nucleus was inhibited by circulating estradiol but did not colocalize with Kiss1 mRNA. Third, about half of isolated ARC Kiss1 neurons expressed Tacr1 (NK1R) and 100% Tacr3 (NK3R); for anteroventral-periventricular Kiss1 neurons andGnRHneurons, approximately one-fourth expressed Tacr1 and one-tenth Tacr3; Tacr2 (NK2R) expression was absent in all cases. Overall, these results identify a potent regulation of gonadotropin release by the SP/NK1R and NKA/NK2R systems in the presence of kisspeptin-Kiss1r signaling, indicating that they may, along with NKB/NK3R, control GnRH release, at least in part through actions on Kiss1 neurons. Copyright © 2015 by the Endocrine Society. | URI: | https://hdl.handle.net/11499/10500 https://doi.org/10.1210/en.2014-1651 |
ISSN: | 0013-7227 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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