Please use this identifier to cite or link to this item: 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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