Literature DB >> 20807512

Estrogen signaling in hypothalamic circuits controlling reproduction.

Martin J Kelly1, Jian Qiu.   

Abstract

It is well known that many of the actions of 17β-estradiol (E2) in the central nervous system are mediated via intracellular receptor/transcription factors that interact with steroid response elements on target genes. However, there is compelling evidence for membrane steroid receptors for estrogen in hypothalamic and other brain neurons. Yet, it is not well understood how estrogen signals via membrane receptors and how these signals impact not only membrane excitability but also gene transcription in neurons that modulate GnRH neuronal excitability. Indeed, it has been known for some time that E2 can rapidly alter neuronal activity within seconds, indicating that some cellular effects can occur via membrane delimited events. In addition, E2 can affect second messenger systems including calcium mobilization and a plethora of kinases to alter cell signaling. Therefore, this review will consider our current knowledge of rapid membrane-initiated and intracellular signaling by E2 in hypothalamic neurons critical for reproductive function.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20807512      PMCID: PMC3070154          DOI: 10.1016/j.brainres.2010.08.082

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  102 in total

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8.  Rapid signaling of estrogen in hypothalamic neurons involves a novel G-protein-coupled estrogen receptor that activates protein kinase C.

Authors:  Jian Qiu; Martha A Bosch; Sandra C Tobias; David K Grandy; Thomas S Scanlan; Oline K Ronnekleiv; Martin J Kelly
Journal:  J Neurosci       Date:  2003-10-22       Impact factor: 6.167

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Review 10.  Rapid effects of estrogen on G protein-coupled receptor activation of potassium channels in the central nervous system (CNS).

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Review 7.  Peptides from Natural or Rationally Designed Sources Can Be Used in Overweight, Obesity, and Type 2 Diabetes Therapies.

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