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靛玉红及其衍生物的药理学性质。

Pharmacological properties of indirubin and its derivatives.

机构信息

School of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

School of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Biomed Pharmacother. 2022 Jul;151:113112. doi: 10.1016/j.biopha.2022.113112. Epub 2022 May 20.

Abstract

BACKGROUND

Indirubin is the main bioactive component of the traditional Chinese medicine Indigo naturalis and is a bisindole alkaloid. Multiple studies have shown that indirubin exhibits good anticancer, anti-inflammatory and neuroprotective properties.

METHODS

The purpose of this review is to provide a summary of the pharmacological mechanisms of indirubin and its derivatives.

RESULTS

Indirubin and its derivatives exert anticancer effects by regulating the expression of cyclin-dependent kinases (CDKs), GSK-3β, Bax, Bcl-2, C-MYC, matrix metalloproteinases (MMPs), and focal adhesion kinase (FAK) through the PI3K/AKT/mTOR, nuclear factor (NF)-κB, mitogen-activated protein kinase (MAPK), JAK/signal transducer and activator of transcription 3 (STAT3) pathways and other signaling pathways. We also reviewed the anti-inflammatory and neuroprotective properties of indirubin and its derivatives.

CONCLUSION

The findings of recent studies assessing indirubin and its derivatives suggest that these compounds can be used as potential drugs to treat tumors, inflammation, neuropathy and bacterial infection.

摘要

背景

靛玉红是中药青黛的主要生物活性成分,也是双吲哚生物碱。多项研究表明,靛玉红具有良好的抗癌、抗炎和神经保护作用。

方法

本综述的目的是总结靛玉红及其衍生物的药理学机制。

结果

靛玉红及其衍生物通过调节细胞周期蛋白依赖性激酶(CDKs)、GSK-3β、Bax、Bcl-2、C-MYC、基质金属蛋白酶(MMPs)和黏着斑激酶(FAK)的表达,发挥抗癌作用,其作用机制涉及 PI3K/AKT/mTOR、核因子(NF)-κB、丝裂原活化蛋白激酶(MAPK)、JAK/信号转导和转录激活因子 3(STAT3)等信号通路。我们还综述了靛玉红及其衍生物的抗炎和神经保护作用。

结论

最近评估靛玉红及其衍生物的研究结果表明,这些化合物可作为治疗肿瘤、炎症、神经病变和细菌感染的潜在药物。

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