Department of Biochemistry, Vellalar College for Women (Autonomous), Thindal, Erode, Tamil Nadu, India.
Centre for Biological Sciences, Department of Biochemistry, K.S. Rangasamy College of Arts and Science (Autonomous), Tiruchengode, Tamilnadu, India.
Drug Chem Toxicol. 2022 Sep;45(5):1951-1962. doi: 10.1080/01480545.2021.1894707. Epub 2021 Mar 15.
In the present study, we assessed the therapeutic potential of Biochanin-A (BCA) (10 mg/kg BW/day) pretreatment for 30 days on lipid metabolic abnormalities, proinflammatory cytokines and matrix metalloproteinase expression in isoproterenol (ISO)-induced myocardial infarction (MI) in rats. We measured the potential role of BCA on tissue and circulatory lipid profiles as well as on lipid metabolic enzymes: serum inflammatory cytokines (TNF-α, IL-1α, IL-1β, IL-6 and MCP1) and serum Matrix Metalloproteinases (particularly, MMP-2 and MMP-9) together with mRNA expressions of TNF-α, IL-6, MMP-2 and MMP-9 by RT-PCR analysis. Administration of ISO to rats significantly distorted their lipid metabolism and augmented inflammatory process, MMP expression and proteolytic activity. In addition, pretreatment with BCA of ISO-induced MI rats significantly reestablished the altered lipid metabolism and concealed the inflammation of cytokines. BCA suppressed the expressions of proinflammatory cytokines and MMPs in ISO-induced MI in rats when compared to normal untreated MI rats. Hence, these results established that BCA could improve the pathological processes of myocardial remodeling which was confirmed by histopathology of heart in MI rats and might be an effective beneficial ingredient for the management of heart failure disorders.
在本研究中,我们评估了 Biochanin-A(BCA)(10mg/kgBW/天)预处理 30 天对异丙肾上腺素(ISO)诱导的大鼠心肌梗死(MI)中脂质代谢异常、促炎细胞因子和基质金属蛋白酶表达的治疗潜力。我们测量了 BCA 在组织和循环脂质谱以及脂质代谢酶上的潜在作用:血清炎症细胞因子(TNF-α、IL-1α、IL-1β、IL-6 和 MCP1)和血清基质金属蛋白酶(特别是 MMP-2 和 MMP-9)以及 TNF-α、IL-6、MMP-2 和 MMP-9 的 mRNA 表达通过 RT-PCR 分析。ISO 给药显著改变了大鼠的脂质代谢并增强了炎症过程、MMP 表达和蛋白水解活性。此外,BCA 预处理 ISO 诱导的 MI 大鼠显著恢复了改变的脂质代谢,并掩盖了细胞因子的炎症。与未经治疗的正常 MI 大鼠相比,BCA 抑制了 ISO 诱导的 MI 大鼠中促炎细胞因子和 MMP 的表达。因此,这些结果表明 BCA 可以改善心肌重构的病理过程,这在 MI 大鼠心脏的组织病理学中得到了证实,并且可能是心力衰竭疾病管理的有效有益成分。