Evidence mapPaperPMID 41886752Full record

ArticleActa physiologica (Oxford, England)2026

Angiotensin-(1-7) Alleviates Isoproterenol-Induced Cardiac Hypertrophy by Suppressing Autophagy and Apoptosis Through the Synergistic Action of Mas Receptor and Angiotensin II Type 2 Receptor.

Xiaomei Wang, Fei Guo, Xiaoqian Wang, Yu Guo, Siyao Fan, Lan Hong, Honghua Jin

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Article in Acta physiologica (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Xiaomei WangCollege of Pharmacy, Yanbian University, Yanji, China.ORCID https://orcid.org/0009-0003-3629-4303
Fei GuoCollege of Pharmacy, Yanbian University, Yanji, China.
Xiaoqian WangCollege of Pharmacy, Yanbian University, Yanji, China.
Yu GuoCollege of Pharmacy, Yanbian University, Yanji, China.
Siyao FanDepartment of Physiology and Pathophysiology, College of Medicine, Yanbian University, Yanji, China.
Lan HongDepartment of Physiology and Pathophysiology, College of Medicine, Yanbian University, Yanji, China.ORCID https://orcid.org/0000-0003-1010-6039
Honghua JinDepartment of Pharmacy, Yanbian University Hospital, Yanbian University, Yanji, China.ORCID https://orcid.org/0000-0001-8578-9378

Funding

National Natural Science Foundation of China 81860077
6 · The paper itself

Abstract

aimThe aim of this study is to determine whether Angiotensin-(1-7) [Ang-(1-7)] alleviates isoproterenol (ISO)-induced cardiac hypertrophy by suppressing excessive autophagy and apoptosis through coordinated Mas receptor (MasR) and angiotensin II type-2 receptor (AT

methodsISO-induced hypertrophy was established in mice and assessed by echocardiography, histology, and hypertrophic markers. H9c2 cardiomyocytes were exposed to ISO and treated separately with A-779 (MasR antagonist), PD123319 (AT

resultsAng-(1-7) attenuated ventricular dysfunction, myocardial enlargement, and upregulation of hypertrophic markers in mice with ISO-induced hypertrophy. Pharmacological inhibition with A-779 and PD123319 revealed that Ang-(1-7) actions require reciprocal regulation between MasR and AT

conclusionAng-(1-7) ameliorates ISO-induced cardiac hypertrophy by suppressing excessive autophagy and apoptosis via synergistic MasR-AT

Indexed as

Angiotensin IApoptosisAutophagyCardiomegalyPeptide FragmentsProto-Oncogene ProteinsReceptor, Angiotensin, Type 2Receptors, G-Protein-CoupledAnimalsIsoproterenolMaleMiceMice, Inbred C57BLMyocytes, CardiacProto-Oncogene MasSignal TransductionAngiotensin Iangiotensin I (1-7)IsoproterenolPeptide FragmentsProto-Oncogene MasProto-Oncogene ProteinsReceptor, Angiotensin, Type 2Receptors, G-Protein-Coupledangiotensin‐(1–7)angiotensin II type‐2 receptorapoptosisautophagycardiac hypertrophymas receptor

Identifiers

PMID41886752
PMCPMC13021233

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.