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<p>One of the key components of cardiac damage is myocardial ischemia/reperfusion (MI/R), which damages the heart’s tissues. The soy-based isoflavone glycitin (GLY) has demonstrated anti-inflammatory, anti-oxidative, and osteoporosis effects. This study aimed to investigate the cardioprotective effects of GLY against MI/R-induced myocardial injury and to elucidate its underlying molecular mechanisms. The levels of Malondialdehyde (MDA), glutathione peroxidase (GSH-Px), lactate dehydrogenase (LDH), creatine kinase (CK), tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and superoxide dismutase (SOD) in cardiac tissue and serum were quantified using enzyme-linked immunosorbent assay (ELISA). Hematoxylin-eosin (HE) staining was used to analyze histological alterations in cardiac tissue. Further, Western blotting was employed to evaluate the expression of Akt, PI3K, and nuclear factor-κB (NF-κB) p65. According to the findings, GLY pretreatment significantly attenuated ST-segment elevation (ST) on the electrocardiogram, indicating myocardial protection. In MI/R-injured rats, GLY treatment also decreased levels of LDH, CK, CK-MB, MDA, nitric oxide (NO), and aspartate aminotransferase (AST) while increasing SOD, GSH-Px, and catalase (CAT) efficiency. Furthermore, GLY dose-dependently upregulated PI3K, Akt, and Bcl-2 expression, while downregulating NF-κB p65 and Bax compared with the untreated MI/R group. These results imply that GLY prevents myocardial ischemia/reperfusion injury by inhibiting NF-κB-mediated oxidative stress and apoptosis and stimulating the PI3K/Akt pathway.</p>

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Glycitin Alleviates Myocardial Ischemia-reperfusion Injury By Suppressing Oxidative Stress and Apoptosis Through PI3K/Akt/NF-κB Pathway Modulation

  • 期刊论文

  • 发表日期：

    2026年3月28日

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  • Jie Ding,
  • Yanan Wang,
  • Xiaoling Fang

摘要

One of the key components of cardiac damage is myocardial ischemia/reperfusion (MI/R), which damages the heart’s tissues. The soy-based isoflavone glycitin (GLY) has demonstrated anti-inflammatory, anti-oxidative, and osteoporosis effects. This study aimed to investigate the cardioprotective effects of GLY against MI/R-induced myocardial injury and to elucidate its underlying molecular mechanisms. The levels of Malondialdehyde (MDA), glutathione peroxidase (GSH-Px), lactate dehydrogenase (LDH), creatine kinase (CK), tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and superoxide dismutase (SOD) in cardiac tissue and serum were quantified using enzyme-linked immunosorbent assay (ELISA). Hematoxylin-eosin (HE) staining was used to analyze histological alterations in cardiac tissue. Further, Western blotting was employed to evaluate the expression of Akt, PI3K, and nuclear factor-κB (NF-κB) p65. According to the findings, GLY pretreatment significantly attenuated ST-segment elevation (ST) on the electrocardiogram, indicating myocardial protection. In MI/R-injured rats, GLY treatment also decreased levels of LDH, CK, CK-MB, MDA, nitric oxide (NO), and aspartate aminotransferase (AST) while increasing SOD, GSH-Px, and catalase (CAT) efficiency. Furthermore, GLY dose-dependently upregulated PI3K, Akt, and Bcl-2 expression, while downregulating NF-κB p65 and Bax compared with the untreated MI/R group. These results imply that GLY prevents myocardial ischemia/reperfusion injury by inhibiting NF-κB-mediated oxidative stress and apoptosis and stimulating the PI3K/Akt pathway.