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综述:五味子甲素的药理学和药代动力学。

A review: Pharmacology and pharmacokinetics of Schisandrin A.

机构信息

State Key Laboratory of Southwestern Chinese Medicine Resources, Key Laboratory of Standardization for Chinese Herbal Medicine, Ministry of Education, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Phytother Res. 2022 Jun;36(6):2375-2393. doi: 10.1002/ptr.7456. Epub 2022 Apr 5.

Abstract

Schisandrin A (SA) is a bioactive lignan isolated from the traditional Chinese medicine Fructus schisandrae chinensis. In recent years, it has attracted extensive attention because of its multiple pharmacological activities. This review is the first to provide an overview of SA-related pharmacological effects and pharmacokinetic characteristics. The results showed that SA had many pharmacological effects, such as antiinflammation, anticancer, hepatoprotection, antioxidation, neuroprotection, antidiabetes mellitus, and musculoskeletal protection. Among them, NF-κB, Nrf2, MAPK, NLRP3, PI3K/AKT, Wnt, miRNA, P-gp, CYP450, PXR, and other signal transduction pathways are involved. Pharmacokinetic studies showed that SA had good pharmacokinetic characteristics, but these were affected by other factors, such as drugs or hepatic fibrosis. Thus, SA has a variety of pharmacological effects and good pharmacokinetic characteristics, which is worthy of further research and development in the future.

摘要

五味子甲素(SA)是从中药五味子中分离得到的一种生物活性木脂素。近年来,由于其多种药理活性,引起了广泛关注。这是第一篇综述五味子甲素相关药理作用和药代动力学特征的文章。结果表明,SA 具有多种药理作用,如抗炎、抗癌、保肝、抗氧化、神经保护、抗糖尿病和肌肉骨骼保护。其中涉及 NF-κB、Nrf2、MAPK、NLRP3、PI3K/AKT、Wnt、miRNA、P-gp、CYP450、PXR 等信号转导通路。药代动力学研究表明,SA 具有良好的药代动力学特征,但这些特征受到其他因素的影响,如药物或肝纤维化。因此,SA 具有多种药理作用和良好的药代动力学特征,值得进一步研究和开发。

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