Sex differences in the regulation of Kiss1/NKB neurons in juvenile mice: implications for the timing of puberty.

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  • Author(s): Kauffman AS;Kauffman AS; Navarro VM; Kim J; Clifton DK; Steiner RA
  • Source:
    American journal of physiology. Endocrinology and metabolism [Am J Physiol Endocrinol Metab] 2009 Nov; Vol. 297 (5), pp. E1212-21. Date of Electronic Publication: 2009 Sep 15.
  • Publication Type:
    Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
  • Language:
    English
  • Additional Information
    • Source:
      Publisher: American Physiological Society Country of Publication: United States NLM ID: 100901226 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1522-1555 (Electronic) Linking ISSN: 01931849 NLM ISO Abbreviation: Am J Physiol Endocrinol Metab Subsets: MEDLINE
    • Publication Information:
      Original Publication: Bethesda, MD. : American Physiological Society
    • Subject Terms:
    • Abstract:
      In mammals, puberty onset typically occurs earlier in females than in males, but the explanation for sexual differentiation in the tempo of pubertal development is unknown. Puberty in both sexes is a brain-dependent phenomenon and involves alterations in the sensitivity of neuronal circuits to gonadal steroid feedback as well as gonadal hormone-independent changes in neuronal circuitry. Kisspeptin, encoded by the Kiss1 gene, plays an essential but ill-defined role in pubertal maturation. Neurokinin B (NKB) is coexpressed with Kiss1 in the arcuate nucleus (ARC) and is also important for puberty. We tested whether sex differences in the timing of pubertal development are attributable to sexual differentiation of gonadal hormone-independent mechanisms regulating hypothalamic Kiss1/NKB gene expression. We found that, in juvenile females, gonadotropin secretion and expression of Kiss1 and NKB in the ARC increased immediately following ovariectomy, suggesting that prepubertal females have negligible gonadal hormone-independent restraint on their reproductive axis. In contrast, in similarly aged juvenile males, no changes occurred in LH levels or Kiss1 or NKB expression following castration, suggesting that gonadal hormone-independent mechanisms restrain kisspeptin/NKB-dependent activation of the male reproductive axis before puberty. Notably, adult mice of both sexes showed comparable rapid increases in Kiss1/NKB expression and LH secretion following gonadectomy, signifying that sex differences in the regulation of ARC Kiss1/NKB neurons are manifest only during peripubertal development. Our findings demonstrate that the mechanisms controlling pubertal activation of reproduction in mice are different between the sexes and suggest that gonadal hormone-independent central restraint on pubertal timing involves Kiss1/NKB neurons in the ARC.
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    • Grant Information:
      K99 HD056157 United States HD NICHD NIH HHS; HD-056157 United States HD NICHD NIH HHS; R00 HD056157 United States HD NICHD NIH HHS; U54-HD-12629 United States HD NICHD NIH HHS; U54-HD-28934 United States HD NICHD NIH HHS; U54 HD012303 United States HD NICHD NIH HHS; P50 HD012303 United States HD NICHD NIH HHS; HD-049651 United States HD NICHD NIH HHS
    • Accession Number:
      0 (Gonadal Steroid Hormones)
      0 (Kiss1 protein, mouse)
      0 (Kisspeptins)
      0 (RNA, Messenger)
      3XMK78S47O (Testosterone)
      86933-75-7 (Neurokinin B)
      9002-67-9 (Luteinizing Hormone)
    • Publication Date:
      Date Created: 20090917 Date Completed: 20120313 Latest Revision: 20220321
    • Publication Date:
      20240829
    • Accession Number:
      PMC2781353
    • Accession Number:
      10.1152/ajpendo.00461.2009
    • Accession Number:
      19755669