Modulation of Gonadotrophin-Releasing Hormone Secretion by an Endogenous Circadian Clock
The mechanisms mediating positive feedback effects of oestradiol on pre‐ovulatory gonadotrophin releasing‐hormone (GnRH) surge generation in female mammals, although well‐explored, are still incompletely understood. In addition to binding to and signalling through classical nuclear receptor‐mediated...
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Published in | Journal of neuroendocrinology Vol. 21; no. 4; pp. 339 - 345 |
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Main Authors | , , , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.04.2009
Blackwell |
Subjects | |
Online Access | Get full text |
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Summary: | The mechanisms mediating positive feedback effects of oestradiol on pre‐ovulatory gonadotrophin releasing‐hormone (GnRH) surge generation in female mammals, although well‐explored, are still incompletely understood. In addition to binding to and signalling through classical nuclear receptor‐mediated pathways in afferent hypothalamic neurones, recent evidence suggests that ovarian steroids may use membrane‐bound receptors or nonclassical signalling pathways to directly influence cell function leading to the generation of GnRH surge secretion. We review recent investigations into the role of the endogenous molecular circadian clock on modulation of GnRH gene expression and neuropeptide secretion, and will explore potential molecular mechanisms by which ovarian steroids may directly induce secretory changes at the level of the GnRH neurone, examining closely whether circadian clock gene oscillations may be involved. |
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Bibliography: | istex:53362E19AC6960E70EF8B2AFE94A16DEBE9623C0 ark:/67375/WNG-QX6KSJ9G-9 ArticleID:JNE1845 Present address: Department of Biology, Western Oregon University, Monmouth, OR 97361, USA. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-3 ObjectType-Review-1 |
ISSN: | 0953-8194 1365-2826 |
DOI: | 10.1111/j.1365-2826.2009.01845.x |