S14G-humanin confers cardioprotective effects against chronic adrenergic and pressure overload-induced heart failure in mice

S14G-humanin (HNG), an analog of the mitochondria-derived peptide humanin, has demonstrated protective effects against various cardiovascular diseases. However, the specific pharmacological effects of HNG in heart failure (HF) have not been previously reported. Therefore, in this study, we aimed to...

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Main Authors: Qi Zhao, Ming-Ming Cai, Dan Li, Bin-Yi Zhao, Shuang-Shan Zhou, Zhen-Ru Wu, Yu-Jun Shi, Li Su
Format: Article
Language:English
Published: Elsevier 2023-11-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844023091004
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author Qi Zhao
Ming-Ming Cai
Dan Li
Bin-Yi Zhao
Shuang-Shan Zhou
Zhen-Ru Wu
Yu-Jun Shi
Li Su
author_facet Qi Zhao
Ming-Ming Cai
Dan Li
Bin-Yi Zhao
Shuang-Shan Zhou
Zhen-Ru Wu
Yu-Jun Shi
Li Su
author_sort Qi Zhao
collection DOAJ
description S14G-humanin (HNG), an analog of the mitochondria-derived peptide humanin, has demonstrated protective effects against various cardiovascular diseases. However, the specific pharmacological effects of HNG in heart failure (HF) have not been previously reported. Therefore, in this study, we aimed to investigate the potential protective effect of HNG in HF using a mouse model. HF was induced in mice through intraperitoneal injection of isoproterenol or transverse aortic constriction, followed by separate administration of HNG to assess its therapeutic impact. Our results revealed that HNG treatment significantly delayed the onset of cardiac dysfunction and structural remodeling in the HF mouse model. Furthermore, HNG administration was associated with reduced infiltration of inflammatory cells, improved myocardial fibrosis, and attenuation of cardiomyocyte apoptosis in the treated cardiac tissues. Additionally, we identified the involvement of the transforming growth factor-beta signaling pathway in the beneficial effects of HNG in isoproterenol-induced HF mice. Collectively, these findings underscore the therapeutic potential of HNG in preventing the progression of HF, as demonstrated in two distinct HF mouse models.
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spelling doaj.art-d7751c7546314afa95f2068e8b1c7b1b2023-12-02T07:04:35ZengElsevierHeliyon2405-84402023-11-01911e21892S14G-humanin confers cardioprotective effects against chronic adrenergic and pressure overload-induced heart failure in miceQi Zhao0Ming-Ming Cai1Dan Li2Bin-Yi Zhao3Shuang-Shan Zhou4Zhen-Ru Wu5Yu-Jun Shi6Li Su7Department of Cardiology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, ChinaDepartment of Cardiology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, ChinaDepartment of Cardiology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, ChinaDepartment of Cardiology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, ChinaDepartment of Cardiology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, ChinaLaboratory of Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, ChinaLaboratory of Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, ChinaDepartment of Cardiology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China; Corresponding author. Department of Cardiology, The Second Affiliated Hospital of Chongqing Medical University, No. 288 Tianwen Avenue, Nan'an District, Chongqing, 401336, China.S14G-humanin (HNG), an analog of the mitochondria-derived peptide humanin, has demonstrated protective effects against various cardiovascular diseases. However, the specific pharmacological effects of HNG in heart failure (HF) have not been previously reported. Therefore, in this study, we aimed to investigate the potential protective effect of HNG in HF using a mouse model. HF was induced in mice through intraperitoneal injection of isoproterenol or transverse aortic constriction, followed by separate administration of HNG to assess its therapeutic impact. Our results revealed that HNG treatment significantly delayed the onset of cardiac dysfunction and structural remodeling in the HF mouse model. Furthermore, HNG administration was associated with reduced infiltration of inflammatory cells, improved myocardial fibrosis, and attenuation of cardiomyocyte apoptosis in the treated cardiac tissues. Additionally, we identified the involvement of the transforming growth factor-beta signaling pathway in the beneficial effects of HNG in isoproterenol-induced HF mice. Collectively, these findings underscore the therapeutic potential of HNG in preventing the progression of HF, as demonstrated in two distinct HF mouse models.http://www.sciencedirect.com/science/article/pii/S2405844023091004S14G-humaninHeart failureCardiac remodelingTGF-β
spellingShingle Qi Zhao
Ming-Ming Cai
Dan Li
Bin-Yi Zhao
Shuang-Shan Zhou
Zhen-Ru Wu
Yu-Jun Shi
Li Su
S14G-humanin confers cardioprotective effects against chronic adrenergic and pressure overload-induced heart failure in mice
Heliyon
S14G-humanin
Heart failure
Cardiac remodeling
TGF-β
title S14G-humanin confers cardioprotective effects against chronic adrenergic and pressure overload-induced heart failure in mice
title_full S14G-humanin confers cardioprotective effects against chronic adrenergic and pressure overload-induced heart failure in mice
title_fullStr S14G-humanin confers cardioprotective effects against chronic adrenergic and pressure overload-induced heart failure in mice
title_full_unstemmed S14G-humanin confers cardioprotective effects against chronic adrenergic and pressure overload-induced heart failure in mice
title_short S14G-humanin confers cardioprotective effects against chronic adrenergic and pressure overload-induced heart failure in mice
title_sort s14g humanin confers cardioprotective effects against chronic adrenergic and pressure overload induced heart failure in mice
topic S14G-humanin
Heart failure
Cardiac remodeling
TGF-β
url http://www.sciencedirect.com/science/article/pii/S2405844023091004
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