Cargando…

Sacubitril/Valsartan Inhibits Cardiomyocyte Hypertrophy in Angiotensin II-Induced Hypertensive Mice Independent of a Blood Pressure-Lowering Effect

BACKGROUND: Hypertensive left ventricular hypertrophy is associated with the risk of heart failure, coronary heart disease and cerebrovascular disease. Although sacubitril/valsartan (SAC/VAL), a first-in-class angiotensin receptor neprilysin inhibitor, reduces the risks of death and hospitalization...

Descripción completa

Detalles Bibliográficos
Autores principales: Tashiro, Kohei, Kuwano, Takashi, Ideishi, Akihito, Morita, Hidetaka, Idemoto, Yoshiaki, Goto, Masaki, Suematsu, Yasunori, Miura, Shin-ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666593/
https://www.ncbi.nlm.nih.gov/pubmed/33224383
http://dx.doi.org/10.14740/cr1137
_version_ 1783610161472995328
author Tashiro, Kohei
Kuwano, Takashi
Ideishi, Akihito
Morita, Hidetaka
Idemoto, Yoshiaki
Goto, Masaki
Suematsu, Yasunori
Miura, Shin-ichiro
author_facet Tashiro, Kohei
Kuwano, Takashi
Ideishi, Akihito
Morita, Hidetaka
Idemoto, Yoshiaki
Goto, Masaki
Suematsu, Yasunori
Miura, Shin-ichiro
author_sort Tashiro, Kohei
collection PubMed
description BACKGROUND: Hypertensive left ventricular hypertrophy is associated with the risk of heart failure, coronary heart disease and cerebrovascular disease. Although sacubitril/valsartan (SAC/VAL), a first-in-class angiotensin receptor neprilysin inhibitor, reduces the risks of death and hospitalization for patients with heart failure, its mechanism of action is not fully understood. We hypothesized that SAC/VAL is superior to other conventional drugs in reducing cardiac hypertrophy. METHODS: Male C57BL/6J mice were implanted with an osmotic pump containing angiotensin II (Ang II). After 7 days of Ang II infusion, mice were also treated with either SAC/VAL, valsartan, enalapril or vehicle alone each day for 2 weeks. Blood pressure measurement was done weekly, and echocardiography was performed before and 3 weeks after infusion of Ang II. Histological analyses were done using extracted heart to investigate cardiac hypertrophy and fibrosis. RESULTS: Ang II markedly elevated blood pressures in all of the treatment groups, and there were no differences in the degree of blood pressure reduction among the SAC/VAL-, valsartan- and enalapril-treated groups. Echocardiography showed that SAC/VAL significantly suppressed the increase in left ventricular (LV) wall thickness and tended to decrease LV mass. In a histological analysis, SAC/VAL inhibited Ang II-induced cardiomyocyte hypertrophy, and individual cardiomyocytes in the SAC/VAL group were smaller than those in the valsartan and enalapril groups. Although previous studies using animal models of heart failure have indicated that SAC/VAL attenuates cardiac fibrosis, we found no supporting evidence in this setting. CONCLUSIONS: SAC/VAL, valsartan and enalapril all attenuated cardiomyocyte hypertrophy in a mouse model of Ang II-induced cardiac hypertrophy. Of note, SAC/VAL most strongly suppressed hypertrophy in spite of similar blood pressure-lowering effects as valsartan and enalapril. The present study suggests that SAC/VAL may have a beneficial effect on the early stage of hypertensive heart disease.
format Online
Article
Text
id pubmed-7666593
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elmer Press
record_format MEDLINE/PubMed
spelling pubmed-76665932020-11-20 Sacubitril/Valsartan Inhibits Cardiomyocyte Hypertrophy in Angiotensin II-Induced Hypertensive Mice Independent of a Blood Pressure-Lowering Effect Tashiro, Kohei Kuwano, Takashi Ideishi, Akihito Morita, Hidetaka Idemoto, Yoshiaki Goto, Masaki Suematsu, Yasunori Miura, Shin-ichiro Cardiol Res Original Article BACKGROUND: Hypertensive left ventricular hypertrophy is associated with the risk of heart failure, coronary heart disease and cerebrovascular disease. Although sacubitril/valsartan (SAC/VAL), a first-in-class angiotensin receptor neprilysin inhibitor, reduces the risks of death and hospitalization for patients with heart failure, its mechanism of action is not fully understood. We hypothesized that SAC/VAL is superior to other conventional drugs in reducing cardiac hypertrophy. METHODS: Male C57BL/6J mice were implanted with an osmotic pump containing angiotensin II (Ang II). After 7 days of Ang II infusion, mice were also treated with either SAC/VAL, valsartan, enalapril or vehicle alone each day for 2 weeks. Blood pressure measurement was done weekly, and echocardiography was performed before and 3 weeks after infusion of Ang II. Histological analyses were done using extracted heart to investigate cardiac hypertrophy and fibrosis. RESULTS: Ang II markedly elevated blood pressures in all of the treatment groups, and there were no differences in the degree of blood pressure reduction among the SAC/VAL-, valsartan- and enalapril-treated groups. Echocardiography showed that SAC/VAL significantly suppressed the increase in left ventricular (LV) wall thickness and tended to decrease LV mass. In a histological analysis, SAC/VAL inhibited Ang II-induced cardiomyocyte hypertrophy, and individual cardiomyocytes in the SAC/VAL group were smaller than those in the valsartan and enalapril groups. Although previous studies using animal models of heart failure have indicated that SAC/VAL attenuates cardiac fibrosis, we found no supporting evidence in this setting. CONCLUSIONS: SAC/VAL, valsartan and enalapril all attenuated cardiomyocyte hypertrophy in a mouse model of Ang II-induced cardiac hypertrophy. Of note, SAC/VAL most strongly suppressed hypertrophy in spite of similar blood pressure-lowering effects as valsartan and enalapril. The present study suggests that SAC/VAL may have a beneficial effect on the early stage of hypertensive heart disease. Elmer Press 2020-12 2020-11-02 /pmc/articles/PMC7666593/ /pubmed/33224383 http://dx.doi.org/10.14740/cr1137 Text en Copyright 2020, Tashiro et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tashiro, Kohei
Kuwano, Takashi
Ideishi, Akihito
Morita, Hidetaka
Idemoto, Yoshiaki
Goto, Masaki
Suematsu, Yasunori
Miura, Shin-ichiro
Sacubitril/Valsartan Inhibits Cardiomyocyte Hypertrophy in Angiotensin II-Induced Hypertensive Mice Independent of a Blood Pressure-Lowering Effect
title Sacubitril/Valsartan Inhibits Cardiomyocyte Hypertrophy in Angiotensin II-Induced Hypertensive Mice Independent of a Blood Pressure-Lowering Effect
title_full Sacubitril/Valsartan Inhibits Cardiomyocyte Hypertrophy in Angiotensin II-Induced Hypertensive Mice Independent of a Blood Pressure-Lowering Effect
title_fullStr Sacubitril/Valsartan Inhibits Cardiomyocyte Hypertrophy in Angiotensin II-Induced Hypertensive Mice Independent of a Blood Pressure-Lowering Effect
title_full_unstemmed Sacubitril/Valsartan Inhibits Cardiomyocyte Hypertrophy in Angiotensin II-Induced Hypertensive Mice Independent of a Blood Pressure-Lowering Effect
title_short Sacubitril/Valsartan Inhibits Cardiomyocyte Hypertrophy in Angiotensin II-Induced Hypertensive Mice Independent of a Blood Pressure-Lowering Effect
title_sort sacubitril/valsartan inhibits cardiomyocyte hypertrophy in angiotensin ii-induced hypertensive mice independent of a blood pressure-lowering effect
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666593/
https://www.ncbi.nlm.nih.gov/pubmed/33224383
http://dx.doi.org/10.14740/cr1137
work_keys_str_mv AT tashirokohei sacubitrilvalsartaninhibitscardiomyocytehypertrophyinangiotensiniiinducedhypertensivemiceindependentofabloodpressureloweringeffect
AT kuwanotakashi sacubitrilvalsartaninhibitscardiomyocytehypertrophyinangiotensiniiinducedhypertensivemiceindependentofabloodpressureloweringeffect
AT ideishiakihito sacubitrilvalsartaninhibitscardiomyocytehypertrophyinangiotensiniiinducedhypertensivemiceindependentofabloodpressureloweringeffect
AT moritahidetaka sacubitrilvalsartaninhibitscardiomyocytehypertrophyinangiotensiniiinducedhypertensivemiceindependentofabloodpressureloweringeffect
AT idemotoyoshiaki sacubitrilvalsartaninhibitscardiomyocytehypertrophyinangiotensiniiinducedhypertensivemiceindependentofabloodpressureloweringeffect
AT gotomasaki sacubitrilvalsartaninhibitscardiomyocytehypertrophyinangiotensiniiinducedhypertensivemiceindependentofabloodpressureloweringeffect
AT suematsuyasunori sacubitrilvalsartaninhibitscardiomyocytehypertrophyinangiotensiniiinducedhypertensivemiceindependentofabloodpressureloweringeffect
AT miurashinichiro sacubitrilvalsartaninhibitscardiomyocytehypertrophyinangiotensiniiinducedhypertensivemiceindependentofabloodpressureloweringeffect