Mitochondria-targeting therapeutic strategies for chronic kidney disease.

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Biochemical pharmacology Pub Date : 2025-01-01 Epub Date: 2024-11-27 DOI:10.1016/j.bcp.2024.116669
Annie Sun, Carol A Pollock, Chunling Huang
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引用次数: 0

Abstract

Chronic kidney disease (CKD) is a multifactorial health issue characterised by kidney impairment that has significant morbidity and mortality in the global population. Current treatments for CKD fail to prevent progression to end-stage kidney disease, where management is limited to renal replacement therapy or kidney transplantation. Mitochondrial dysfunction has been implicated in the pathogenesis of CKD and can be broadly categorised into abnormalities related to excessive oxidative stress, reduced mitochondrial biogenesis, excess mitochondrial fission and dysregulated mitophagy. Mitochondria-targeting therapeutic strategies target many of the outlined mechanisms of mitochondrial dysfunction, and an overview of recent evidence for mitochondria-targeting therapeutic strategies is explored in this review, including naturally derived compounds and novel approaches such as fusion proteins. Mitochondria-targeting therapeutic strategies using these approaches show the potential to stabilise or improve renal function, and clinical studies are needed to further confirm their safety and efficacy in human contexts.

慢性肾脏疾病的线粒体靶向治疗策略。
慢性肾脏疾病(CKD)是一种以肾脏损害为特征的多因素健康问题,在全球人口中具有显著的发病率和死亡率。目前CKD的治疗不能防止进展为终末期肾脏疾病,其管理仅限于肾脏替代治疗或肾移植。线粒体功能障碍与CKD的发病机制有关,可大致分为与过度氧化应激、线粒体生物发生减少、线粒体分裂过多和线粒体自噬失调相关的异常。线粒体靶向治疗策略针对许多线粒体功能障碍的机制,并概述了线粒体靶向治疗策略的最新证据,包括天然衍生化合物和融合蛋白等新方法。使用这些方法的线粒体靶向治疗策略显示出稳定或改善肾功能的潜力,需要临床研究进一步证实其在人类环境中的安全性和有效性。
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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