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多囊肾病中的活性氧物种

Reactive Oxygen Species in Cystic Kidney Disease.

作者信息

Subhash Sanat, Vijayvargiya Sonya, Parmar Aetan, Sandhu Jazlyn, Simmons Jabrina, Raina Rupesh

机构信息

Department of Internal Medicine, Northeast Ohio Medical University, Rootstown, OH 44272, USA.

Department of Internal Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Antioxidants (Basel). 2024 Sep 30;13(10):1186. doi: 10.3390/antiox13101186.

DOI:10.3390/antiox13101186
PMID:39456439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11504974/
Abstract

Polycystic kidney disease (PKD) is a rare but significant renal condition with major implications for global acute and chronic patient care. Oxidative stress and reactive oxygen species (ROS) can significantly alter its pathophysiology, clinical outcomes, and treatment, contributing to negative outcomes, including hypertension, chronic kidney disease, and kidney failure. Inflammation from ROS and existing cysts propagate the generation and accumulation of ROS, exacerbating kidney injury, pro-fibrotic signaling cascades, and interstitial fibrosis. Early identification and prevention of oxidative stress and ROS can contribute to reduced cystic kidney disease progression and improved longitudinal patient outcomes. Increased research regarding biomarkers, the pathophysiology of oxidative stress, and novel therapeutic interventions alongside the creation of comprehensive guidelines establishing methods of assessment, monitoring, and intervention for oxidative stress in cystic kidney disease patients is imperative to standardize clinical practice and improve patient outcomes. The integration of artificial intelligence (AI), genetic editing, and genome sequencing could further improve the early detection and management of cystic kidney disease and mitigate adverse patient outcomes. In this review, we aim to comprehensively assess the multifactorial role of ROS in cystic kidney disease, analyzing its pathophysiology, clinical outcomes, treatment interventions, clinical trials, animal models, and future directions for patient care.

摘要

多囊肾病(PKD)是一种罕见但严重的肾脏疾病,对全球急性和慢性患者护理具有重大影响。氧化应激和活性氧(ROS)可显著改变其病理生理学、临床结局和治疗,导致包括高血压、慢性肾脏病和肾衰竭在内的不良后果。ROS引发的炎症和现有囊肿会促使ROS的产生和积累,加剧肾损伤、促纤维化信号级联反应和间质纤维化。早期识别和预防氧化应激及ROS有助于减缓囊性肾病的进展并改善患者的长期预后。加强关于生物标志物、氧化应激病理生理学及新型治疗干预措施的研究,并制定全面的指南,确立评估、监测和干预囊性肾病患者氧化应激的方法,对于规范临床实践和改善患者预后至关重要。人工智能(AI)、基因编辑和基因组测序的整合可进一步改善囊性肾病的早期检测和管理,并减轻患者的不良结局。在本综述中,我们旨在全面评估ROS在囊性肾病中的多因素作用,分析其病理生理学、临床结局、治疗干预、临床试验、动物模型以及患者护理的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f337/11504974/5ce0cf5f1350/antioxidants-13-01186-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f337/11504974/978b3f4df3d1/antioxidants-13-01186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f337/11504974/4388c169f8fe/antioxidants-13-01186-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f337/11504974/5ce0cf5f1350/antioxidants-13-01186-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f337/11504974/978b3f4df3d1/antioxidants-13-01186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f337/11504974/4388c169f8fe/antioxidants-13-01186-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f337/11504974/5ce0cf5f1350/antioxidants-13-01186-g003.jpg

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本文引用的文献

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Emerging Roles of Xanthine Oxidoreductase in Chronic Kidney Disease.黄嘌呤氧化还原酶在慢性肾脏病中的新作用
Antioxidants (Basel). 2024 Jun 12;13(6):712. doi: 10.3390/antiox13060712.
2
Genome editing and kidney health.基因组编辑与肾脏健康。
Clin Kidney J. 2024 Apr 17;17(5):sfae119. doi: 10.1093/ckj/sfae119. eCollection 2024 May.
3
Raising serum uric acid with a uricase inhibitor worsens PKD in rat and mouse models.用尿酸酶抑制剂升高血清尿酸会使大鼠和小鼠模型中的多囊肾病恶化。
Am J Physiol Renal Physiol. 2024 Jun 1;326(6):F1004-F1015. doi: 10.1152/ajprenal.00372.2023. Epub 2024 Apr 18.
4
Genetics of cystogenesis in base-edited human organoids reveal therapeutic strategies for polycystic kidney disease.碱基编辑人类类器官中的囊发生遗传学揭示了多囊肾病的治疗策略。
Cell Stem Cell. 2024 Apr 4;31(4):537-553.e5. doi: 10.1016/j.stem.2024.03.005.
5
Inspiring Tactics with the Improvement of Mitophagy and Redox Balance for the Development of Innovative Treatment against Polycystic Kidney Disease.通过提高自噬和氧化还原平衡来激发策略,为多囊肾病的创新治疗开发提供新的思路。
Biomolecules. 2024 Feb 9;14(2):207. doi: 10.3390/biom14020207.
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An Artificial Intelligence Generated Automated Algorithm to Measure Total Kidney Volume in ADPKD.一种用于测量常染色体显性多囊肾病中总肾体积的人工智能生成的自动化算法。
Kidney Int Rep. 2023 Nov 4;9(2):249-256. doi: 10.1016/j.ekir.2023.10.029. eCollection 2024 Feb.
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AI models for automated segmentation of engineered polycystic kidney tubules.用于自动分割工程化多囊肾病管腔的 AI 模型。
Sci Rep. 2024 Feb 3;14(1):2847. doi: 10.1038/s41598-024-52677-1.
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Real-life use of tolvaptan in ADPKD: a retrospective analysis of a large Canadian cohort.托伐普坦在 ADPKD 中的实际应用:一项加拿大大型队列的回顾性分析。
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Feasibility and impact of ketogenic dietary interventions in polycystic kidney disease: KETO-ADPKD-a randomized controlled trial.生酮饮食干预多囊肾病的可行性和影响:KETO-ADPKD-一项随机对照试验。
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Allopurinol and oxypurinol differ in their strength and mechanisms of inhibition of xanthine oxidoreductase.别嘌醇和氧嘌呤醇在抑制黄嘌呤氧化还原酶的强度和机制方面存在差异。
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