Advances and Perspectives on the Anti-Fibrotic Mechanisms of the Quercetin.

IF 5.5
The American journal of Chinese medicine Pub Date : 2025-01-01 Epub Date: 2025-07-07 DOI:10.1142/S0192415X25500545
Xiaoqin Liu, Qingzhi Liang, Yufeng Qin, Zhengtao Chen, Rensong Yue
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Abstract

Fibrosis is a pathological process that affects multiple tissues and organs and a significant contributor to mortality, particularly in developed countries. Dietary flavonoids, especially quercetin (QUR), have emerged as key bioactive compounds with protective effects on vital organs such as the liver, heart, lungs, and kidneys. As a prominent focus in natural product research, QUR exhibits diverse anti-fibrotic mechanisms across various fibrotic conditions, including modulation of the TGF-[Formula: see text], NF-[Formula: see text]B, Nrf2, and AREG/EGFR signaling pathways. This review consolidates current knowledge on QUR and its derivatives, covering their anti-fibrotic mechanisms, drug interactions, pharmacokinetics, safety, and toxicological profiles. It offers insights for developing novel QUR-based formulations. Our findings highlight QUR's potential, which is supported by substantial evidence, as a natural therapeutic agent in functional foods and dietary supplements that target fibrosis. However, further high-quality studies are essential to validate its safety, optimize formulation stability, and confirm clinical efficacy in order to ultimately expand its therapeutic applications.

槲皮素抗纤维化机制研究进展及展望。
纤维化是一种影响多个组织和器官的病理过程,是造成死亡率的重要因素,特别是在发达国家。膳食类黄酮,尤其是槲皮素(QUR),已经成为对肝脏、心脏、肺和肾脏等重要器官具有保护作用的关键生物活性化合物。作为天然产物研究的重点,QUR在不同的纤维化条件下表现出不同的抗纤维化机制,包括调节TGF-[公式:见文],NF-[公式:见文]B, Nrf2和AREG/EGFR信号通路。这篇综述整合了目前关于QUR及其衍生物的知识,包括它们的抗纤维化机制、药物相互作用、药代动力学、安全性和毒理学特征。它为开发新的基于qur的配方提供了见解。我们的研究结果强调了QUR的潜力,这是有大量证据支持的,作为针对纤维化的功能性食品和膳食补充剂的天然治疗剂。然而,为了最终扩大其治疗应用,需要进一步的高质量研究来验证其安全性、优化配方稳定性和确认临床疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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