Evidence map›Paper›PMID 41345537›Full record

ArticleBMC cardiovascular disorders2025

Resveratrol suppresses susceptibility of ventricular arrhythmia in heart failure model.

Yung-Nan Tsai, Ya-Wen Hsiao, Ting-Yung Chang, Chen-Chung Liao, Chin-Yu Lin, Yu-Cheng Hsieh, Tze-Fan Chao, Guan-Yi Li, Yu-Ting Huang, Satoshi Higa and 2 more

Abstract read
In one paragraph

Article in BMC cardiovascular disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yung-Nan TsaiDivision of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Ya-Wen HsiaoDivision of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Ting-Yung ChangDivision of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Chen-Chung LiaoCancer and Immunology Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Chin-Yu LinDivision of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Yu-Cheng HsiehCardiovascular Center, Taichung Veterans General Hospital, Taichung, Taiwan.
Tze-Fan ChaoDivision of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Guan-Yi LiCardiovascular Center, Taichung Veterans General Hospital, Taichung, Taiwan.
Yu-Ting HuangDivision of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Satoshi HigaDivision of Cardiovascular Medicine, Cardiac Electrophysiology and Pacing Laboratory, Makiminato Central Hospital, Okinawa, Japan.
Shih-Ann ChenDivision of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Shih-Lin ChangDivision of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan. ep.slchang@msa.hinet.net.

Funding

Foundation for the Development of Internal Medicine in Okinawa 5-02-007Ministry of Science and Technology, Taiwan MOST106-2314-B-010-035-MY3SZU-YUAN Research Foundation of Internal Medicine 111003Taipei Veterans General Hospital V108C-055
6 · The paper itself

Abstract

backgroundThis study investigated the efficacy of resveratrol in reducing ventricular arrhythmia (VA) and modulating calcium handling in a heart failure (HF) model.

methodsHF rabbits were established five weeks after coronary artery ligation. The groups included control, HF rabbits, and HF rabbits treated with intraperitoneal injections of resveratrol 2.5 mg/kg (HF + Res group) in the last week. The electrophysiology of the left ventricle (LV) was investigated using epicardial optical mapping. The action potential duration (APD), calcium transient duration (CaiTD), level of fibrosis and apoptosis, and protein and mRNA levels of ion channels and calcium-handling proteins were also measured.

resultsThe HF group demonstrated a reduction in LV ejection fraction, an augmentation in APD80 and CaiTD80, and an escalation in VA inducibility. The administration of resveratrol resulted in the restoration of cardiac function, a reduction in APD80 and CaiTD80, and a decrease in VA, phase singularities, and dominant frequency. In HF, the expression of ion channels such as Cav1.2, RyR, Nav1.5, Kv1.4, Kv1.5, and Kir2.1 was significantly decreased. The level of SERCA2a, a calcium pump essential for intracellular calcium regulation, was also reduced. Treatment with resveratrol effectively restored the expression of these proteins. Concurrently, HF-induced elevations in fibrosis (collagen I), apoptosis (caspase-3), and inflammation (NF-κB) were significantly attenuated by resveratrol. Proteomic profiling further revealed differential regulation of ion channel–associated proteins and enrichment of cardioprotective signaling pathways, underscoring the therapeutic potential of resveratrol in HF.

conclusionsResveratrol ameliorates calcium handling, reverses structural and electrical remodeling, and suppresses VA in a rabbit HF model.

Indexed as

Anti-Arrhythmia AgentsArrhythmias, CardiacCalcium SignalingHeart FailureHeart RateMyocytes, CardiacResveratrolTachycardia, VentricularVentricular Function, LeftAction PotentialsAnimalsApoptosisDisease Models, AnimalFibrosisMaleRabbitsAnti-Arrhythmia AgentsResveratrolCalcium handlingHeart failureIon channelsOptical mappingVentricular arrhythmia

Identifiers

PMID41345537
PMCPMC12781752

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Registered trials

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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 OpenQuestion graph.