Literature DB >> 26939826

Rapid estrogen actions on ion channels: A survey in search for mechanisms.

Lee-Ming Kow1, Donald W Pfaff2.   

Abstract

A survey of nearly two hundred reports shows that rapid estrogenic actions can be detected across a range of kinds of estrogens, a range of doses, on a wide range of tissue, cell and ion channel types. Striking is the fact that preparations of estrogenic agents that do not permeate the cell membrane almost always mimic the actions of the estrogenic agents that do permeate the membrane. All kinds of estrogens, ranging from natural ones, through receptor modulators, endocrine disruptors, phytoestrogens, agonists, and antagonists to novel G-1 and STX, have been reported to be effective. For actions on specific types of ion channels, the possibility of opposing actions, in different cases, is the rule, not the exception. With this variety there is no single, specific action mechanism for estrogens per se, although in some cases estrogens can act directly or via some signaling pathways to affect ion channels. We infer that estrogens can bind a large number of substrates/receptors at the membrane surface. As against the variety of subsequent routes of action, this initial step of the estrogen's binding action is the key.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  BK; Estrogen binding; Ion channel kinetics; L-type Ca(2+) channel; Selective Estrogen Receptor Modulator (SERM); Signaling pathway

Mesh:

Substances:

Year:  2016        PMID: 26939826      PMCID: PMC4929851          DOI: 10.1016/j.steroids.2016.02.018

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  189 in total

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3.  Rapid non-genomic activation of cytosolic cyclic AMP-dependent protein kinase activity and [Ca(2+)](i) by 17beta-oestradiol in female rat distal colon.

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Journal:  Br J Pharmacol       Date:  2000-04       Impact factor: 8.739

4.  Environmental estrogenic pollutants induce acute vascular relaxation by inhibiting L-type Ca2+ channels in smooth muscle cells.

Authors:  D O Ruehlmann; J R Steinert; M A Valverde; R Jacob; G E Mann
Journal:  FASEB J       Date:  1998-05       Impact factor: 5.191

5.  Estradiol inhibits Ca2+ and K+ channels in smooth muscle cells from pregnant rat myometrium.

Authors:  K Okabe; Y Inoue; H Soeda
Journal:  Eur J Pharmacol       Date:  1999-07-02       Impact factor: 4.432

6.  Pharmacologic preconditioning of estrogen by activation of the myocardial adenosine triphosphate-sensitive potassium channel in patients undergoing coronary angioplasty.

Authors:  Tsung Ming Lee; Sheng Fang Su; Tsai Fwu Chou; Chang Her Tsai
Journal:  J Am Coll Cardiol       Date:  2002-03-06       Impact factor: 24.094

7.  17-beta-estradiol activates maxi-K channels through a non-genomic pathway in human breast cancer cells.

Authors:  Guyllaume Coiret; Fabrice Matifat; Frédéric Hague; Halima Ouadid-Ahidouch
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8.  The phytoestrogen ginsensoside Re activates potassium channels of vascular smooth muscle cells through PI3K/Akt and nitric oxide pathways.

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2.  Estradiol-modified prolactin secretion independently of action potentials and Ca2+ and blockade of outward potassium currents in GH3 cells.

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3.  Testosterone decreases urinary bladder smooth muscle excitability via novel signaling mechanism involving direct activation of the BK channels.

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Review 4.  Sex differences in the brain: Implications for behavioral and biomedical research.

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Review 6.  Endocrine disruption by dietary phyto-oestrogens: impact on dimorphic sexual systems and behaviours.

Authors:  Heather B Patisaul
Journal:  Proc Nutr Soc       Date:  2016-07-08       Impact factor: 6.297

7.  Equilin displays similar endothelium-independent vasodilator potential to 17β-estradiol regardless of lower potential to inhibit calcium entry.

Authors:  Fernando P Filgueira; Núbia S Lobato; Denise L Nascimento; Graziela S Ceravolo; Fernanda R C Giachini; Victor V Lima; Ana Paula Dantas; Zuleica B Fortes; R Clinton Webb; Rita C Tostes; Maria Helena C Carvalho
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8.  Screening the ToxCast phase II libraries for alterations in network function using cortical neurons grown on multi-well microelectrode array (mwMEA) plates.

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Review 9.  The Interface of Nuclear and Membrane Steroid Signaling.

Authors:  Lindsey S Treviño; Daniel A Gorelick
Journal:  Endocrinology       Date:  2021-08-01       Impact factor: 4.736

10.  Hormonal gain control of a medial preoptic area social reward circuit.

Authors:  Jenna A McHenry; James M Otis; Mark A Rossi; J Elliott Robinson; Oksana Kosyk; Noah W Miller; Zoe A McElligott; Evgeny A Budygin; David R Rubinow; Garret D Stuber
Journal:  Nat Neurosci       Date:  2017-01-30       Impact factor: 24.884

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