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辅酶 Q10 在急性肾损伤中肾脏保护作用的分子机制。

Molecular mechanisms underlying the renal protective effects of coenzyme Q10 in acute kidney injury.

机构信息

Department of Urology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, 318000, Zhejiang, China.

Department of Urology, Maoming People's Hospital, Maoming, 525000, Guangdong, China.

出版信息

Cell Mol Biol Lett. 2022 Jul 22;27(1):57. doi: 10.1186/s11658-022-00361-5.


DOI:10.1186/s11658-022-00361-5
PMID:35869439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9308331/
Abstract

Coenzyme Q10 (CoQ10), an endogenous antioxidant, has been reported frequently to exert an outstanding protective effect on multiple organ injury, including acute kidney injury (AKI). In this study, we aim to summarize all the current evidence of the protective action of CoQ10 against AKI as there are presently no relevant reviews in the literature. After a systematic search, 20 eligible studies, either clinical trials or experimental studies, were included and further reviewed. CoQ10 treatment exhibited a potent renal protective effect on various types of AKI, such as AKI induced by drugs (e.g., ochratoxin A, cisplatin, gentamicin, L-NAME, and nonsteroidal anti-inflammatory drug), extracorporeal shock wave lithotripsy (ESWL), sepsis, contrast media, and ischemia-reperfusion injury. The renal protective role of CoQ10 against AKI might be mediated by the antiperoxidative, anti-apoptotic, and anti-inflammatory potential of CoQ10. The molecular mechanisms for the protective effects of CoQ10 might be attributed to the regulation of multiple essential genes (e.g., caspase-3, p53, and PON1) and signaling cascades (e.g., Nrf2/HO-1 pathway). This review highlights that CoQ10 may be a potential strategy in the treatment of AKI.

摘要

辅酶 Q10(CoQ10)作为一种内源性抗氧化剂,常被报道对多种器官损伤具有显著的保护作用,包括急性肾损伤(AKI)。在本研究中,我们旨在总结 CoQ10 对 AKI 的保护作用的所有现有证据,因为目前文献中尚无相关综述。经过系统检索,纳入了 20 项符合条件的研究,包括临床试验和实验研究,并进一步进行了综述。CoQ10 治疗对各种类型的 AKI (如药物诱导的 AKI (如赭曲霉毒素 A、顺铂、庆大霉素、L-NAME 和非甾体抗炎药)、体外冲击波碎石术(ESWL)、脓毒症、造影剂和缺血再灌注损伤)均表现出强大的肾脏保护作用。CoQ10 对 AKI 的肾脏保护作用可能是通过 CoQ10 的抗过氧化、抗凋亡和抗炎潜力介导的。CoQ10 保护作用的分子机制可能归因于对多种必需基因(如 caspase-3、p53 和 PON1)和信号级联(如 Nrf2/HO-1 途径)的调节。本综述强调,CoQ10 可能是治疗 AKI 的一种潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e11/9308331/178372ab28e2/11658_2022_361_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e11/9308331/9681a456f978/11658_2022_361_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e11/9308331/178372ab28e2/11658_2022_361_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e11/9308331/9681a456f978/11658_2022_361_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e11/9308331/178372ab28e2/11658_2022_361_Fig2_HTML.jpg

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[8]
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本文引用的文献

[1]
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.

Kidney Int. 2022-9

[2]
Serum IL-17 levels are higher in critically ill patients with AKI and associated with worse outcomes.

Crit Care. 2022-4-14

[3]
Anti-cancer peptide-based therapeutic strategies in solid tumors.

Cell Mol Biol Lett. 2022-4-9

[4]
Antioxidant and Anti-Inflammatory Effects of Coenzyme Q10 Supplementation on Infectious Diseases.

Healthcare (Basel). 2022-3-7

[5]
Serum Level of Complement C1q is Associated with Contrast-Associated Acute Kidney Injury in Patients Undergoing Emergency Percutaneous Coronary Intervention.

J Inflamm Res. 2021-12-24

[6]
Non-embryotoxic dosage of alternariol aggravates ochratoxin A-triggered deleterious effects on embryonic development through ROS-dependent apoptotic processes.

Toxicol Res (Camb). 2021-11-28

[7]
Prediction of Postoperative Sepsis Based on Changes in Presepsin Levels of Critically Ill Patients with Acute Kidney Injury after Abdominal Surgery.

Diagnostics (Basel). 2021-12-9

[8]
Delivery of coenzyme Q10 with mitochondria-targeted nanocarrier attenuates renal ischemia-reperfusion injury in mice.

Mater Sci Eng C Mater Biol Appl. 2021-12

[9]
Recent advances in nanotherapeutics for the treatment and prevention of acute kidney injury.

Asian J Pharm Sci. 2021-7

[10]
Shift in MSL1 alternative polyadenylation in response to DNA damage protects cancer cells from chemotherapeutic agent-induced apoptosis.

Cell Rep. 2021-10-12

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