4.5 Article

The Integrated Hypothalamic Tachykinin-Kisspeptin System as a Central Coordinator for Reproduction

Journal

ENDOCRINOLOGY
Volume 156, Issue 2, Pages 627-637

Publisher

ENDOCRINE SOC
DOI: 10.1210/en.2014-1651

Keywords

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Funding

  1. Eunice Kennedy Shriver National Institute of Child Health and Human Development, Specialized Cooperative Centers Program in Reproduction and Infertility Research grants from the National Institute of Health [U54 HD028138]
  2. National Institutes of Health (NIH) [R01 HD019938]
  3. Charles H. Hood Foundation for Child Health Research Program
  4. Microgrant Program from The Biomedical Research Institute
  5. Center for Faculty Development and Diversity's Office for Research Careers at the Brigham and Women's Hospital
  6. Scientific and Technological Research Council of Turkey [2219]
  7. NIH [K99 HD071970, R01 NS043330, R01 DK068098]

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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, decreased LH release in ovariectomized-sham replaced females, as documented for NK3R 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 and GnRH neurons, 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.

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