4.4 Article

Physiological role of metastin/kisspeptin in regulating gonadotropin-releasing hormone (GnRH) secretion in female rats

Journal

PEPTIDES
Volume 30, Issue 1, Pages 49-56

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.peptides.2008.08.004

Keywords

Pulse; Surge; Estrous cycle; Estrogen; Lactation; Suckling stimulus

Funding

  1. Program for Promotion of Basic Research Activities for Innovative Biosciences (PROBRAIN) of Japan
  2. Japanese Ministry of Education, Culture, Sports, Science and Technology [19380157]

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Various studies have attempted to unravel the physiological role of metastin/kisspeptin in the control of gonadotropin-releasing hormone (GnRH) release. A number of evidences suggested that the population of metastin/kisspeptin neurons in the anteroventral periventricular nucleus (AVPV) is involved in generating a GnRH surge to induce ovulation in rodents, and thus the target of estrogen positive feedback. Females have an obvious metastin/kisspeptin neuronal population in the AVPV, but males have only a few cell bodies in the nucleus, suggesting that the absence of the surge-generating mechanism or positive feedback action in males is due to the limited AVPV metastin/kisspeptin neuronal population. On the other hand, the arcuate nucleus (ARC) metastin/kisspeptin neuronal population is considered to be involved in the regulation of tonic GnRH release. The ARC metastin/kisspeptin neurons show no sex difference in their expression, which is suppressed by gonadal steroids in both sexes. Thus, the ARC population of metastin/kisspeptin neurons is a target of estrogen negative feedback action on tonic GnRH release. The lactating rat model provided further evidence indicating that ARC in etastin/kisspeptin neurons are involved in GnRH pulse generation, because pulsatile release of luteinizing hormone (LH) is profoundly suppressed by suckling stimulus and the LH pulse suppression is well associated with the suppression of ARC metastin/kisspeptin and KISS-1 gene expression in lactating rats. (C) 2008 Elsevier Inc. All rights reserved.

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