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绞股蓝总苷通过调节 PI3K/Akt/Bad 通路抑制动脉粥样硬化内皮细胞凋亡。

Gypenoside Inhibits Endothelial Cell Apoptosis in Atherosclerosis by Modulating Mitochondria through PI3K/Akt/Bad Pathway.

机构信息

Key Laboratory of Ministry of Education for TCM Viscera-State Theory and Applications, Liaoning University of Traditional Chinese Medicine, Shenyang 110847, China.

National Local Joint Engineering Laboratory for the Prevention and Treatment of Cardioencephalopathy with Integrated Traditional Chinese and Western Medicine, Shenyang 110847, China.

出版信息

Biomed Res Int. 2020 Jun 20;2020:2819658. doi: 10.1155/2020/2819658. eCollection 2020.

Abstract

Atherosclerosis remains the most common cause of deaths worldwide. Endothelial cell apoptosis is an important process in the progress of atherosclerosis, as it can cause the endothelium to lose their capability in regulating the lipid homeostasis, inflammation, and immunity. Endothelial cell injury can disrupt the integrity and barrier function of an endothelium and facilitate lipid deposition, leading to atherogenesis. Chinese medicine techniques for preventing and treating atherosclerosis are gaining attention, especially natural products. In this study, we demonstrated that gypenoside could decrease the levels of serum lipid, alleviate the formation of atherosclerotic plaque, and lessen aortic intima thickening. Gypenoside potentially activates the PI3K/Akt/Bad signal pathway to modulate the apoptosis-related protein expression in the aorta. Moreover, gypenoside downregulated mitochondrial fission and fusion proteins, mitochondrial energy-related proteins in the mouse aorta. In conclusion, this study demonstrated a new function of gypenoside in endothelial apoptosis and suggested a therapeutic potential of gypenoside in atherosclerosis associated with apoptosis by modulating mitochondrial function through the PI3K/Akt/Bad pathway.

摘要

动脉粥样硬化仍然是全世界最常见的死亡原因。内皮细胞凋亡是动脉粥样硬化进展中的一个重要过程,因为它会导致内皮失去调节脂质稳态、炎症和免疫的能力。内皮细胞损伤会破坏内皮的完整性和屏障功能,并促进脂质沉积,导致动脉粥样硬化形成。预防和治疗动脉粥样硬化的中药技术越来越受到关注,尤其是天然产物。在这项研究中,我们证明了绞股蓝皂苷可以降低血清脂质水平,减轻动脉粥样硬化斑块的形成,减少主动脉内膜增厚。绞股蓝皂苷可能通过激活 PI3K/Akt/Bad 信号通路来调节主动脉中与细胞凋亡相关的蛋白表达。此外,绞股蓝皂苷下调了小鼠主动脉中的线粒体分裂和融合蛋白以及线粒体能量相关蛋白。总之,这项研究证明了绞股蓝皂苷在血管内皮细胞凋亡中的新功能,并通过 PI3K/Akt/Bad 通路调节线粒体功能,提示绞股蓝皂苷在与凋亡相关的动脉粥样硬化治疗方面具有潜在的作用。

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