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黄连素治疗纤维化的药理机制研究进展

Advances in the pharmacological mechanisms of berberine in the treatment of fibrosis.

作者信息

Liu Xiaoqin, Liang Qingzhi, Wang Yifan, Xiong Shuai, Yue Rensong

机构信息

Department of Endocrinology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.

Clinical Medical School, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.

出版信息

Front Pharmacol. 2024 Sep 20;15:1455058. doi: 10.3389/fphar.2024.1455058. eCollection 2024.

Abstract

The rising incidence of fibrosis poses a major threat to global public health, and the continuous exploration of natural products for the effective treatment of fibrotic diseases is crucial. Berberine (BBR), an isoquinoline alkaloid, is widely used clinically for its anti-inflammatory, anti-tumor and anti-fibrotic pharmacological effects. Until now, researchers have worked to explore the mechanisms of BBR for the treatment of fibrosis, and multiple studies have found that BBR attenuates fibrosis through different pathways such as TGF-β/Smad, AMPK, Nrf2, PPAR-γ, NF-κB, and Notch/snail axis. This review describes the anti-fibrotic mechanism of BBR and its derivatives, and the safety evaluation and toxicity studies of BBR. This provides important therapeutic clues and strategies for exploring new drugs for the treatment of fibrosis. Nevertheless, more studies, especially clinical studies, are still needed. We believe that with the continuous implementation of high-quality studies, significant progress will be made in the treatment of fibrosis.

摘要

纤维化发病率的上升对全球公共卫生构成了重大威胁,持续探索用于有效治疗纤维化疾病的天然产物至关重要。黄连素(BBR)是一种异喹啉生物碱,因其抗炎、抗肿瘤和抗纤维化药理作用而在临床上广泛应用。到目前为止,研究人员一直在探索BBR治疗纤维化的机制,多项研究发现BBR通过TGF-β/Smad、AMPK、Nrf2、PPAR-γ、NF-κB和Notch/snail轴等不同途径减轻纤维化。本文综述了BBR及其衍生物的抗纤维化机制,以及BBR的安全性评价和毒性研究。这为探索治疗纤维化的新药提供了重要的治疗线索和策略。然而,仍需要更多的研究,尤其是临床研究。我们相信,随着高质量研究的不断开展,纤维化的治疗将取得重大进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c704/11450235/e1535b713397/fphar-15-1455058-g001.jpg

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