Key result
Quisqualis indica extract reduces oxidative indicators and myocardial necrosis in a rat myocardial infarction model.
Why the study?
Myocardial infarction is a major global cause of morbidity and death driven by ischemic heart disease and oxidative stress, and the cardioprotective potential of Quisqualis indica extract remained to be evaluated in experimental models.
Does ethanolic extract of Quisqualis indica improve oxidative and histopathological markers in an isoproterenol-induced myocardial infarction rat model?
Does ethanolic extract of Quisqualis indica improve oxidative and histopathological markers in an isoproterenol-induced myocardial infarction rat model?
Quisqualis indica extract demonstrates cardioprotective effects in a rat model of myocardial infarction by reducing oxidative stress and myocardial damage.
EQI attenuates oxidative damage in rat MI model; hypothesis-generating, leaves open human translation.
Introduction: Myocardial infarction (MI) is one of the most common causes of morbidity and death globally, driven by ischemic heart disease and oxidative stress. Quisqualis indica (Q. indica), a plant traditionally used in Chinese medicine, is recognized for its therapeutic potential due to its rich phytochemical profile, which includes flavonoids, alkaloids, and tannins. Objectives: The objective of this study is to evaluate the cardioprotective potential of the ethanolic extract of Quisqualis indica using established experimental models. The study aims to assess its effect on key biochemical, histopathological, and functional cardiac parameters. The phytochemical constituents responsible for these effects will be explored, with emphasis on quercetin and related flavonoids. Ultimately, the study intends to establish Q. indica as a potential natural therapeutic agent for cardiovascular disorders. results: Results indicated that EQI dramatically reduced oxidative indicators by lowering malondialdehyde (MDA) levels and restored the antioxidant enzymes like superoxide dismutase (SOD), glutathione (GSH), and catalase. Histopathological analysis showed reduced myocardial necrosis, oedema, and fibrosis in EQI-treated groups compared to the ISO control group, confirming the cardioprotective potential of Q. indica. Methods: This study investigates the cardioprotective efficacy of an ethanolic extract of Q. indica (EQI) in an isoproterenol (ISO)-induced MI rat model. Experimental groups were pretreated with EQI, and the extract’s effects on various biochemical markers were evaluated. Results and discussion: Results indicated that EQI significantly reduced oxidative indicators by lowering malondialdehyde (MDA) levels and restoring antioxidant enzymes such as superoxide dismutase (SOD), glutathione (GSH), and catalase. Histopathological analysis showed reduced myocardial necrosis, edema, and fibrosis in EQI-treated groups compared to the ISO control group, confirming the cardioprotective potential of Q. indica. Conclusion: These findings suggest that Q. indica may serve as a natural therapeutic agent against MI through its antioxidative properties, potentially paving the way for the development of novel, plant-based cardioprotective treatments.
No takes yet. Share an insight, caveat, or question.
Rathore et al. (2026) studied Myocardial infarction. Ethanolic extract of Quisqualis indica (EQI) vs. Isoproterenol (ISO) control group was evaluated on Oxidative indicators and histopathological changes. Ethanolic extract of Quisqualis indica reduced oxidative indicators and myocardial necrosis compared to control in an isoproterenol-induced myocardial infarction rat model.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: