山奈酚的潜在肾脏保护作用:生物合成、作用机制和临床前景。

IF 2.1 Q3 PHARMACOLOGY & PHARMACY Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2024-09-30 eCollection Date: 2024-01-01 DOI:10.1155/2024/8907717
Maulana Yusuf Alkandahri, Asman Sadino, Barolym Tri Pamungkas, Zulpakor Oktoba, Maya Arfania, Nia Yuniarsih, Eko Sri Wahyuningsih, Yuliani Dewi, Sri Ayu Winarti, Sri Tantia Dinita
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引用次数: 0

摘要

肾脏是一个重要器官,极易受到血液中各种有毒物质造成的细胞损伤。多项研究表明,该器官的损伤如不及时治疗,会导致肾小球硬化、肾小管间质纤维化和肾小管细胞凋亡,从而导致肾功能衰竭。尽管现代治疗取得了重大进展,但目前还没有完全有效的药物来修复肾脏功能、提供全面保护和帮助细胞再生。此外,据报道,一些现有药物会加重损伤,因此有必要探索替代治疗方法。目前,人们正在探索将天然药物作为治疗肾脏疾病的新策略。山奈酚是一种存在于蔬菜、豆类和水果等植物中的多酚,已在各种肾毒性实验中被广泛研究。据报道,该化合物具有肾保护剂的潜力,对各种生理途径都有益处,如 CPL 诱导的肾损伤、DOX、LPO、ROS、RCC 和糖尿病肾病。因此,本研究旨在概述目前山奈酚的肾保护作用及其分子作用机制、生物合成途径和临床前景。
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Potential Nephroprotective Effect of Kaempferol: Biosynthesis, Mechanisms of Action, and Clinical Prospects.

Kidney is an essential organ that is highly susceptible to cellular injury caused by various toxic substances in the blood. Several studies have shown that untreated injuries to this organ can cause glomerulosclerosis, tubulointerstitial fibrosis, and tubular cell apoptosis, leading to kidney failure. Despite significant advancements in modern treatment, there is no fully effective drug for repairing its function, providing complete protection, and assisting in cell regeneration. Furthermore, some available medications have been reported to exacerbate injuries, showing the need to explore alternative treatments. Natural drugs are currently being explored as a new therapeutic strategy for managing kidney diseases. Kaempferol, a polyphenol found in plants, including vegetables, legumes, and fruits, has been extensively studied in various nephrotoxicity protocols. The compound has been reported to have potential as a nephroprotective agent with beneficial effects on various physiological pathways, such as CPL-induced kidney injury, DOX, LPO, ROS, RCC, and diabetic nephropathy. Therefore, this study aims to provide a brief overview of the current nephroprotective effects of kaempferol, as well as its molecular mechanisms of action, biosynthesis pathways, and clinical prospects.

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来源期刊
CiteScore
4.30
自引率
3.60%
发文量
0
审稿时长
17 weeks
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