Evidence map›Paper›PMID 41699672›Full record

ArticleJournal of cardiothoracic surgery2026

Resveratrol ameliorates myocardial injury and inflammatory response and cell apoptosis in Kawasaki disease rats by activating the Nrf2/HO-1 pathway.

Weiyan Yan, Na Tian

Abstract read
In one paragraph

Article in Journal of cardiothoracic surgery, 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

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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

2 authors.

Weiyan YanDepartment 2 of Children's Internal Medicine, Xi'an International Medical Center Hospital, Xi'an, 710100, Shaanxi Province, China.
Na TianDepartment 2 of Children's Internal Medicine, Xi'an International Medical Center Hospital, Xi'an, 710100, Shaanxi Province, China. 15877689239@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKawasaki disease (KD) is an acute, self-limiting systemic vasculitis of unknown etiology, which often involves the coronary arteries, leading to severe complications such as myocardial injury (MI). It aimed to explore the mechanism of action of Resveratrol (RES) on MI induced by KD in rats based on the Nrf2/HO-1 pathway. 

methodsThirty-six rats were randomly grouped: control, model, RES intervention, Nrf2 inhibitor + RES intervention groups (CG, MG, RG, IRG). The KD rat model was established. After modeling, RES was administered to the RG via intraperitoneal injection, while sterile saline was injected into the CG and MG. Cardiac function, inflammatory factors in myocardial tissue, and related proteins was examined.

resultsAs against the MG, the left ventricular end-diastolic diameter (LVEDd) and left ventricular end-systolic diameter (LVESd) were visibly reduced, while left ventricular ejection fraction (LVEF) and left ventricular fractional shortening (LVFS) were visibly increased in the RG; The levels of inflammatory factors in the RG were visibly decreased but still higher relative to the CG; The relative expression (RE) of Nrf2 and HO-1 in the RG was visibly increased but still lower relative to the CG; In contrast to the MG, the RE of Bcl2 was visibly higher, while the RE of Bax was visibly lower in the RG (P < 0.05); Compared with the RG, the RE of Nrf2 in the nuclear protein of the IRG was significantly decreased to (0.41 ± 0.03) (P < 0.05).

conclusionRES can improve MI and cardiac dysfunction in KD rats by activating the Nrf2/HO-1 pathway, inhibiting inflammatory response and cell apoptosis, providing theoretical and experimental evidence for its application.

Indexed as

ApoptosisHeme Oxygenase-1Mucocutaneous Lymph Node SyndromeNF-E2-Related Factor 2ResveratrolStilbenesAnimalsDisease Models, AnimalInflammationMaleMyocardiumRatsRats, Sprague-DawleySignal TransductionHeme Oxygenase-1Nfe2l2 protein, ratNF-E2-Related Factor 2ResveratrolStilbenesInflammatory responseKawasaki diseaseMyocardial injuryNrf2/HO-1 pathwayResveratrol

Identifiers

PMID41699672
PMCPMC13014800

What Socratic holds

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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 Socratic graph.