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Baicalin and the liver-gut system: Pharmacological bases explaining its therapeutic effects

期刊

PHARMACOLOGICAL RESEARCH
卷 165, 期 -, 页码 -

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2021.105444

关键词

Baicalin; Liver-gut system; Pharmacological basis; Intestinal flora; Bile acid

资金

  1. National Natural Science Foundation of China [81874365, 81703725]
  2. Sichuan Science and Technology Program [2019YJ0492]
  3. Beijing Medical and Health Foundation [YWJKJJHKYJJ-B20645FN]
  4. Chengdu University of TCM Found Grant [QNXZ2018025]

向作者/读者索取更多资源

Baicalin, extracted from Scutellaria baicalensis Georgi, exerts protective effects on liver and gut diseases by mediating oxidative stress, inflammation, and apoptosis pathways, providing new insights into its pharmacological effects.
With the development of high-throughput screening and bioinformatics technology, natural products with a range of pharmacological targets in multiple diseases have become important sources of new drug discovery. These compounds are derived from various plants, including the dried root of Scutellaria baicalensis Georgi, which is often used as a traditional Chinese herb named Huangqin, a popular medication used for thousands of years in China. Many studies have shown that baicalin, an extract from Scutellaria baicalensis Georgi, exerts various protective effects on liver and gut diseases. Baicalin plays a therapeutic role mainly by mediating downstream apoptosis and immune response pathways induced by upstream oxidative stress and inflammation. During oxidative stress regulation, PI3K/Akt/NRF2, Keap-1, NF-kappa B and HO-1 are key factors associated with the healing effects of baicalin on NAFLD/NASH, ulcerative colitis and cholestasis. In the inflammatory response, IL-6, IL-1 beta, TNF-alpha, MIP-2 and MIP-1a are involved in the alleviation of NAFLD/NASH, cholestasis and liver fibrosis by baicalin, as are TGF-beta 1/Smads, STAT3 and NF-kappa B. Regarding the apoptosis pathway, Bax, Bcl-2, Caspase-3 and Caspase-9 are key factors related to the suppression of hepatocellular carcinoma and attenuation of liver injury and colorectal cancer. In addition to immune regulation, PD-1/PDL-1 and TLR4-NF-kappa B are correlated with the alleviation of hepatocellular carcinoma, ulcerative colitis and colorectal cancer by baicalin. Moreover, baicalin regulates intestinal flora by promoting the production of SCFAs. Furthermore, BA is involved in the interactions of the liver-gut axis by regulating TGR5, FXR, bile acids and the microbiota. In general, a comprehensive analysis of this natural compound was conducted to determine the mechanism by which it regulates bile acid metabolism, the intestinal flora and related signaling pathways, providing new insights into the pharmacological effects of baicalin. The mechanism linking the liver and gut systems needs to be elucidated to draw attention to its great clinical importance.

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