Therapeutic effect of umbilical cord mesenchymal stem cells on renal ischemia-reperfusion injury.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Acta Pharmaceutica Pub Date : 2025-04-10 Print Date: 2025-03-01 DOI:10.2478/acph-2025-0006
Liang Xiao, Chengyu Huang, Shanghua Xiao, Lingfeng Xie, Xueyan Zhang, Fucheng Xiao, Huajia Cai, Shuibo Yang, Shengqing Wu, Shoukang Qu, Jia Liu
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Abstract

Acute kidney injury (AKI) is a growing global health issue with no effective treatments. This study evaluates the therapeutic effects of umbilical cord mesenchymal stem cells (UC-MSCs) on AKI caused by ischemia-reperfusion injury (IRI) in mice. Thirty mice were divided into a sham group, an IRI group, and an MSC-treated group. Renal function was assessed, and histological analysis, immunofluorescence, and real-time PCR were used to evaluate renal damage, inflammatory cell presence, and cytokine expression (TNF-α, IL-6, IL-10). Results showed that MSC treatment reduced renal damage, decreased pro-inflammatory cytokines (TNF-α, IL-6), increased anti-inflammatory IL-10, and promoted kidney repair by homing to injury sites. Thus, umbilical cord MSCs may mitigate AKI by reducing inflammation and enhancing renal repair.

脐带间充质干细胞对肾缺血再灌注损伤的治疗作用。
急性肾损伤(AKI)是一个日益严重的全球性健康问题,目前尚无有效的治疗方法。本研究评价脐带间充质干细胞(UC-MSCs)对小鼠缺血再灌注损伤(IRI)所致AKI的治疗作用。将30只小鼠分为假手术组、IRI组和msc治疗组。评估肾功能,采用组织学分析、免疫荧光和实时荧光定量PCR评估肾脏损害、炎症细胞存在和细胞因子表达(TNF-α、IL-6、IL-10)。结果显示,MSC治疗可减轻肾损伤,降低促炎细胞因子(TNF-α, IL-6),增加抗炎IL-10,并通过损伤部位的归巢促进肾脏修复。因此,脐带间充质干细胞可能通过减少炎症和增强肾脏修复来减轻AKI。
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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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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