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丹参酮IIA药理作用及机制的近期研究进展(2015 - 2021年)与展望

Recent Research Progress (2015-2021) and Perspectives on the Pharmacological Effects and Mechanisms of Tanshinone IIA.

作者信息

Zhong Chenhui, Lin Zuan, Ke Liyuan, Shi Peiying, Li Shaoguang, Huang Liying, Lin Xinhua, Yao Hong

机构信息

Department of Pharmaceutical Analysis, School of Pharmacy, Fujian Medical University, Fuzhou, China.

Department of Traditional Chinese Medicine Resource and Bee Products, College of Animal Sciences (College of Bee Science), Fujian Agriculture and Forestry University, Fuzhou, China.

出版信息

Front Pharmacol. 2021 Nov 8;12:778847. doi: 10.3389/fphar.2021.778847. eCollection 2021.

Abstract

Tanshinone IIA (Tan IIA) is an important characteristic component and active ingredient in , and its various aspects of research are constantly being updated to explore its potential application. In this paper, we review the recent progress on pharmacological activities and the therapeutic mechanisms of Tan IIA according to literature during the years 2015-2021. Tan IIA shows multiple pharmacological effects, including anticarcinogenic, cardiovascular, nervous, respiratory, urinary, digestive, and motor systems activities. Tan IIA modulates multi-targets referring to Nrf2, AMPK, GSK-3β, EGFR, CD36, HO-1, NOX4, Beclin-1, TLR4, TNF-α, STAT3, Caspase-3, and bcl-2 proteins and multi-pathways including NF-κB, SIRT1/PGC1α, MAPK, SREBP-2/Pcsk9, Wnt, PI3K/Akt/mTOR pathways, TGF-β/Smad and Hippo/YAP pathways, etc., which directly or indirectly influence disease course. Further, with the reported targets, the potential effects and possible mechanisms of Tan IIA against diseases were predicted by bioinformatic analysis. This paper provides new insights into the therapeutic effects and mechanisms of Tan IIA against diseases.

摘要

丹参酮IIA(Tan IIA)是[具体事物]中的一种重要特征成分和活性成分,其各方面研究不断更新以探索其潜在应用。本文根据2015 - 2021年间的文献,综述了Tan IIA药理活性及治疗机制的最新进展。Tan IIA具有多种药理作用,包括抗癌、心血管、神经、呼吸、泌尿、消化和运动系统活性。Tan IIA调节涉及Nrf2、AMPK、GSK - 3β、EGFR、CD36、HO - 1、NOX4、Beclin - 1、TLR4、TNF - α、STAT3、Caspase - 3和bcl - 2蛋白的多靶点以及包括NF - κB、SIRT1/PGC1α、MAPK、SREBP - 2/Pcsk9、Wnt、PI3K/Akt/mTOR途径、TGF - β/Smad和Hippo/YAP途径等多途径,这些直接或间接影响疾病进程。此外,结合已报道的靶点,通过生物信息学分析预测了Tan IIA对疾病的潜在作用和可能机制。本文为Tan IIA对疾病的治疗作用和机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6550/8606659/d81d0cf6c7ca/fphar-12-778847-g001.jpg

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