Beta-glucan protects against isoproterenol-induced cardiac remodeling by regulating the ACE-AT1R axis and attenuates cardiac inflammation and apoptosis

Objective: To investigate the cardioprotective effect of beta-glucan against isoproterenol-induced cardiotoxicity in rats, and elucidate the underlying mechanism. Methods: Rats were orally pretreated with beta-glucan (40 mg/kg body weight) for 30 d, and isoproterenol (20 mg/100 g body weight) was ad...

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Main Authors: Anitha Roy, Vasantha Mallenahalli Neelakantappa, Jayashree Ganesan, Balakrishnan Ramajayam Asokan, Srinivasan Kulandaivel, V V Sathibabu Uddandrao, Sengottuvelu Singaravel
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-01-01
Series:Asian Pacific Journal of Tropical Biomedicine
Subjects:
Online Access:http://www.apjtb.org/article.asp?issn=2221-1691;year=2023;volume=13;issue=9;spage=384;epage=392;aulast=Roy
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author Anitha Roy
Vasantha Mallenahalli Neelakantappa
Jayashree Ganesan
Balakrishnan Ramajayam Asokan
Srinivasan Kulandaivel
V V Sathibabu Uddandrao
Sengottuvelu Singaravel
author_facet Anitha Roy
Vasantha Mallenahalli Neelakantappa
Jayashree Ganesan
Balakrishnan Ramajayam Asokan
Srinivasan Kulandaivel
V V Sathibabu Uddandrao
Sengottuvelu Singaravel
author_sort Anitha Roy
collection DOAJ
description Objective: To investigate the cardioprotective effect of beta-glucan against isoproterenol-induced cardiotoxicity in rats, and elucidate the underlying mechanism. Methods: Rats were orally pretreated with beta-glucan (40 mg/kg body weight) for 30 d, and isoproterenol (20 mg/100 g body weight) was administered on days 31 and 32. The effects of beta-glucan on markers of cardiac injury, hemodynamic changes, production of proinflammatory cytokines, and the corresponding mRNA expressions were evaluated. In addition, histological analysis was performed. Results: Pretreatment with beta-glucan prevented isoproterenol-induced cardiac injury by preserving the structural and functional integrity of the plasma membrane and attenuating the production of proinflammatory cytokines (NF-κB, TNF-α, IL-6, IL-Ιβ, and IFN-γ) in the heart. Moreover, beta-glucan significantly downregulated the mRNA expression of ACE, AT1R, TNF-α, IL-6, NF-κB, caspase-3, TLR-4, and Bax, and upregulated Bcl-2 in the heart. At the same time, pretreatment with beta-glucan alleviated myocardial damage as reflected in a reduction in myonecrosis, edema, and erythrocyte extravasation with almost imperceptible inflammation. Conclusions: Beta-glucan can protect against isoproterenol-induced cardiotoxicity by attenuating cardiac inflammation and apoptosis and regulating the ACE-AT1R axis, thereby preventing cardiac remodeling.
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spelling doaj.art-e78fea4f59724dcc90dad908bed957042023-10-26T05:33:09ZengWolters Kluwer Medknow PublicationsAsian Pacific Journal of Tropical Biomedicine2221-16912588-92222023-01-0113938439210.4103/2221-1691.385569Beta-glucan protects against isoproterenol-induced cardiac remodeling by regulating the ACE-AT1R axis and attenuates cardiac inflammation and apoptosisAnitha RoyVasantha Mallenahalli NeelakantappaJayashree GanesanBalakrishnan Ramajayam AsokanSrinivasan KulandaivelV V Sathibabu UddandraoSengottuvelu SingaravelObjective: To investigate the cardioprotective effect of beta-glucan against isoproterenol-induced cardiotoxicity in rats, and elucidate the underlying mechanism. Methods: Rats were orally pretreated with beta-glucan (40 mg/kg body weight) for 30 d, and isoproterenol (20 mg/100 g body weight) was administered on days 31 and 32. The effects of beta-glucan on markers of cardiac injury, hemodynamic changes, production of proinflammatory cytokines, and the corresponding mRNA expressions were evaluated. In addition, histological analysis was performed. Results: Pretreatment with beta-glucan prevented isoproterenol-induced cardiac injury by preserving the structural and functional integrity of the plasma membrane and attenuating the production of proinflammatory cytokines (NF-κB, TNF-α, IL-6, IL-Ιβ, and IFN-γ) in the heart. Moreover, beta-glucan significantly downregulated the mRNA expression of ACE, AT1R, TNF-α, IL-6, NF-κB, caspase-3, TLR-4, and Bax, and upregulated Bcl-2 in the heart. At the same time, pretreatment with beta-glucan alleviated myocardial damage as reflected in a reduction in myonecrosis, edema, and erythrocyte extravasation with almost imperceptible inflammation. Conclusions: Beta-glucan can protect against isoproterenol-induced cardiotoxicity by attenuating cardiac inflammation and apoptosis and regulating the ACE-AT1R axis, thereby preventing cardiac remodeling.http://www.apjtb.org/article.asp?issn=2221-1691;year=2023;volume=13;issue=9;spage=384;epage=392;aulast=Royβeta-glucan; isoproterenol; cardiac inflammation; cardiac apoptosis; cardiovascular diseases; heart failure; myocardial infarction
spellingShingle Anitha Roy
Vasantha Mallenahalli Neelakantappa
Jayashree Ganesan
Balakrishnan Ramajayam Asokan
Srinivasan Kulandaivel
V V Sathibabu Uddandrao
Sengottuvelu Singaravel
Beta-glucan protects against isoproterenol-induced cardiac remodeling by regulating the ACE-AT1R axis and attenuates cardiac inflammation and apoptosis
Asian Pacific Journal of Tropical Biomedicine
βeta-glucan; isoproterenol; cardiac inflammation; cardiac apoptosis; cardiovascular diseases; heart failure; myocardial infarction
title Beta-glucan protects against isoproterenol-induced cardiac remodeling by regulating the ACE-AT1R axis and attenuates cardiac inflammation and apoptosis
title_full Beta-glucan protects against isoproterenol-induced cardiac remodeling by regulating the ACE-AT1R axis and attenuates cardiac inflammation and apoptosis
title_fullStr Beta-glucan protects against isoproterenol-induced cardiac remodeling by regulating the ACE-AT1R axis and attenuates cardiac inflammation and apoptosis
title_full_unstemmed Beta-glucan protects against isoproterenol-induced cardiac remodeling by regulating the ACE-AT1R axis and attenuates cardiac inflammation and apoptosis
title_short Beta-glucan protects against isoproterenol-induced cardiac remodeling by regulating the ACE-AT1R axis and attenuates cardiac inflammation and apoptosis
title_sort beta glucan protects against isoproterenol induced cardiac remodeling by regulating the ace at1r axis and attenuates cardiac inflammation and apoptosis
topic βeta-glucan; isoproterenol; cardiac inflammation; cardiac apoptosis; cardiovascular diseases; heart failure; myocardial infarction
url http://www.apjtb.org/article.asp?issn=2221-1691;year=2023;volume=13;issue=9;spage=384;epage=392;aulast=Roy
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