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人参皂苷 Rb 在心肌缺血再灌注损伤中的分子信号通路:小型综述。

Molecular-Signaling Pathways of Ginsenosides Rb in Myocardial Ischemia-Reperfusion Injury: A Mini Review.

机构信息

Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, 56000 Cheras, Kuala Lumpur, Malaysia.

Cardiovascular Health Research Group, Faculty of Medicine, Universiti Kebangsaan Malaysia, 56000 Cheras, Kuala Lumpur, Malaysia.

出版信息

Int J Med Sci. 2022 Jan 1;19(1):65-73. doi: 10.7150/ijms.64984. eCollection 2022.

Abstract

Reperfusion injury following myocardial ischemia remained a challenge for optimal treatment of myocardial infarction. Ginsenosides Rb (G-Rb), the primary components of ginsenoside, have been reported to exert cardioprotective effects via numerous mechanisms. G-Rb1 mediate cardioprotective effects via various signaling pathways, including mitochondrial apoptotic pathway, PI3K/Akt/mTOR, HIF-1α and GRF91, RhoA, p38α MAPK, and eNOS. G-Rb2 activates the SIRT-1 pathway, while G-Rb3 promotes both JNK-mediated NF-κB and PERK/Nrf2/HMOX1. Generally, ginsenosides Rb1, 2, and 3 modulates oxidative stress, inflammation, and apoptosis, contributing to the improvement of structural, functional and biochemical parameters. In conclusion, G-Rb, particularly G-Rb1, have vast potential as a supplement in attenuating reperfusion injury. Translation into a clinical trial is warranted to confirm the beneficial effects of G-Rb.

摘要

心肌缺血后的再灌注损伤仍然是心肌梗死最佳治疗的挑战。人参皂苷 Rb(G-Rb)作为人参的主要成分之一,据报道通过多种机制发挥心脏保护作用。G-Rb1 通过多种信号通路介导心脏保护作用,包括线粒体凋亡途径、PI3K/Akt/mTOR、HIF-1α 和 GRF91、RhoA、p38α MAPK 和 eNOS。G-Rb2 激活 SIRT-1 途径,而 G-Rb3 促进 JNK 介导的 NF-κB 和 PERK/Nrf2/HMOX1。一般来说,人参皂苷 Rb1、2 和 3 调节氧化应激、炎症和细胞凋亡,有助于改善结构、功能和生化参数。总之,G-Rb,特别是 G-Rb1,作为减轻再灌注损伤的补充剂具有巨大的潜力。需要进行临床试验来证实 G-Rb 的有益作用。

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