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异甜菊醇钠通过调节 Sirt1/AMPK 通路减轻高脂/高胆固醇诱导的心肌功能障碍。

Isosteviol sodium attenuates high fat/high cholesterol-induced myocardial dysfunction by regulating the Sirt1/AMPK pathway.

机构信息

School of Pharmacy, Jinan University, Guangzhou, 510632, China; YZ Health-tech Inc, Hengqin District, Zhuhai, 519000, China.

Institute of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou, 510006, China.

出版信息

Biochem Biophys Res Commun. 2022 Sep 17;621:80-87. doi: 10.1016/j.bbrc.2022.06.044. Epub 2022 Jun 30.

DOI:10.1016/j.bbrc.2022.06.044
PMID:35810595
Abstract

A fat-rich diet triggers obesity, and promotes cardiomyocyte injury. Till now, no prior investigations suggested a beneficial role of Isosteviol Sodium (STVNa) in cardiac activity in high fat diet (HFD)-exposed obese rats. However, there is evidence that STVNa accelerates healing of multiple tissue injuries. Herein, we explored the underlying mechanism behind the STVNa-based protection against HFD-induced myocardial dysfunction (MCD) in a rat model of myocardial injury. We employed dosages of 1, 10, and 20 mg/kg STVNa to treat MCD in rats fed with a HFD. Based on our results, STVNa repressed MCD (as indicated by ecocardiographic analysis), myocardium function, pathological structure, and myocardial enzymes. Mechanistically, the STVNa-mediated protection against HFD-induced MCD involved inhibition of inflammation and oxidative stress. Furthermore, using Western blot analysis, we revealed that the critical members of the Sirt1/AMPK network were markedly activated in the STVNa-treated group, relative to HFD-fed controls. Collectively, these evidences suggested that the STVNa offered strong protection against HFD-induced MCD. Moreover, this effect was mediated by the activation of the Sirt1/AMPK network, which, in turn, promoted lipid metabolism.

摘要

高脂肪饮食会引发肥胖,并促进心肌细胞损伤。到目前为止,没有先前的研究表明异甜醇钠(STVNa)在高脂肪饮食(HFD)暴露肥胖大鼠的心脏活动中有有益作用。然而,有证据表明 STVNa 加速了多种组织损伤的愈合。在此,我们在心肌损伤大鼠模型中探索了 STVNa 对 HFD 诱导的心肌功能障碍(MCD)的保护作用的潜在机制。我们使用 1、10 和 20mg/kg 的 STVNa 剂量来治疗 HFD 喂养的大鼠的 MCD。根据我们的结果,STVNa 抑制了 MCD(如超声心动图分析所示)、心肌功能、病理结构和心肌酶。从机制上讲,STVNa 对 HFD 诱导的 MCD 的保护作用涉及抑制炎症和氧化应激。此外,通过 Western blot 分析,我们发现 Sirt1/AMPK 网络的关键成员在 STVNa 处理组中明显被激活,与 HFD 喂养对照组相比。综上所述,这些证据表明 STVNa 对 HFD 诱导的 MCD 提供了强有力的保护。此外,这种作用是通过激活 Sirt1/AMPK 网络介导的,这反过来又促进了脂质代谢。

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Isosteviol sodium injection improves outcomes by modulating TLRs/NF-κB-dependent inflammatory responses following experimental traumatic brain injury in rats.异甜菊醇钠注射液通过调节大鼠实验性创伤性脑损伤后TLRs/NF-κB依赖性炎症反应改善预后。
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