The effect of oestrogen on Ca2+ and Na+ regulation in heart failure
File(s)Biophysics Abstract_final.docx (18.12 KB)
Accepted version
Author(s)
Firth, Jahn M
Yang, Hsiang-Yu
Francis, Alice J
Alvarez-Laviada, Anita
MacLeod, Kenneth T
Type
Conference Paper
Abstract
In this work, we show that long-term absence of oestrogen impairs cardiac function and produces detrimental changes to Ca2+ and Na+ regulation in cardiomyocytes following pressure-overload heart failure (HF). Oestrogen supplementation reverses the negative effects of ovariectomy following HF.
Pressure-overload HF was induced by aortic constriction (AC) in female guinea pigs. To examine the effects of long-term absence of oestrogen on HF progression, selected ovariectomy (OV) animals underwent AC (ACOV). Pellets containing 17β-oestradiol (1mg, 60-day release) were placed subcutaneously in selected ACOV animals (ACOV+E). Electrophysiological and fluorescence techniques were used to assess Ca2+ and Na+ regulation 150 days post-operatively.
ACOV animals heart weight/body weight ratios increased by 11% and in vivo fractional shortening decreased by 14% compared with the AC group, suggesting greater impairment of cardiac function following pressure-overload in the absence of oestrogen. Action potential duration increased in all three interventions but the changes were oestrogen-independent. While ICa and fractional SR Ca2+ release were unaltered, myocytes from ACOV animals typically had reduced Ca2+ transient amplitudes, slower transient decay kinetics, decreased SR Ca2+ contents and increased Ca2+ spark frequencies and spark mediated SR Ca2+ leak compared with the AC and ACOV+E groups. The Na+/K+ ATPase current densities and Na+ extrusion rates were reduced by 13% and 19%, respectively, in parallel with a 17% increased INa,L current densities following ACOV compared with the AC group. Interestingly, myocytes isolated from ACOV animals supplemented with 17β-oestradiol (ACOV+E) typically had similar Ca2+ and Na+ regulation compared with the gonad-intact AC group.
Here we present that long-term deprivation of oestrogen, in an animal model whose electrophysiological and hormonal status is akin to human, exacerbates the detrimental effects of pressure-overload HF. Oestrogen supplementation reverses the negative effects of ovariectomy following AC.
Pressure-overload HF was induced by aortic constriction (AC) in female guinea pigs. To examine the effects of long-term absence of oestrogen on HF progression, selected ovariectomy (OV) animals underwent AC (ACOV). Pellets containing 17β-oestradiol (1mg, 60-day release) were placed subcutaneously in selected ACOV animals (ACOV+E). Electrophysiological and fluorescence techniques were used to assess Ca2+ and Na+ regulation 150 days post-operatively.
ACOV animals heart weight/body weight ratios increased by 11% and in vivo fractional shortening decreased by 14% compared with the AC group, suggesting greater impairment of cardiac function following pressure-overload in the absence of oestrogen. Action potential duration increased in all three interventions but the changes were oestrogen-independent. While ICa and fractional SR Ca2+ release were unaltered, myocytes from ACOV animals typically had reduced Ca2+ transient amplitudes, slower transient decay kinetics, decreased SR Ca2+ contents and increased Ca2+ spark frequencies and spark mediated SR Ca2+ leak compared with the AC and ACOV+E groups. The Na+/K+ ATPase current densities and Na+ extrusion rates were reduced by 13% and 19%, respectively, in parallel with a 17% increased INa,L current densities following ACOV compared with the AC group. Interestingly, myocytes isolated from ACOV animals supplemented with 17β-oestradiol (ACOV+E) typically had similar Ca2+ and Na+ regulation compared with the gonad-intact AC group.
Here we present that long-term deprivation of oestrogen, in an animal model whose electrophysiological and hormonal status is akin to human, exacerbates the detrimental effects of pressure-overload HF. Oestrogen supplementation reverses the negative effects of ovariectomy following AC.
Date Issued
2018-02-02
Date Acceptance
2017-10-02
Citation
Biophysical Journal, 2018, 114 (3, Supplement 1), pp.617A-617A
ISSN
0006-3495
Publisher
Biophysical Society
Start Page
617A
End Page
617A
Journal / Book Title
Biophysical Journal
Volume
114
Issue
3, Supplement 1
Copyright Statement
© 2018 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/
Sponsor
British Heart Foundation
British Heart Foundation
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000430563300085&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Grant Number
SP/16/2/32004
FS/17/73/33186
Source
62nd Annual Meeting of the Biophysical-Society
Subjects
Science & Technology
Life Sciences & Biomedicine
Biophysics
Publication Status
Published
Start Date
2018-02-17
Finish Date
2018-02-21
Coverage Spatial
San Francisco, CA
Date Publish Online
2018-02-06