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血必净通过抑制中性粒细胞和炎症减轻高压电烧伤所致急性肾损伤。

Xuebijing alleviates high-voltage electrical burn-induced acute kidney injury by inhibiting neutrophils and inflammation.

作者信息

He Xiaopei, Li Na, Ma Leilei, Yang Meng, Ren Liqing, Hao Jiawen, Xue Xin, Pang Yinghui

机构信息

Outpatient Department, Shijiazhuang Tianyimei Medical Aesthetic Hospital, Shijiazhuang, Hebei, China.

Department of Gastrointestinal Diagnosis and Treatment, First Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

出版信息

Sci Rep. 2025 Aug 19;15(1):30410. doi: 10.1038/s41598-025-11977-w.

DOI:10.1038/s41598-025-11977-w
PMID:40830157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12365283/
Abstract

This study aimed to investigate the clinical effect of Xuebijing in alleviating acute kidney injury (AKI) after high-voltage electrical burns by inhibiting neutrophils, inflammatory cells, and its potential influence on reactive oxygen species (ROS). Ninety-six patients with AKI following high-voltage electrical burns, admitted to our hospital from February 2023 to December 2024, were included. They were randomized using a computer-generated random number sequence into two groups: a study group (Xuebijing, n = 48) and a control group (n = 48). This study was conducted in an open-label manner. Neutrophil, inflammatory cell, and ROS levels, as well as kidney function and oxidative stress factors (SOD, MDA), were compared at baseline (1 h before treatment) and 7 days post-treatment. Adverse reactions were recorded. The sample size was determined based on previous similar studies indicating clinically significant differences with comparable group sizes. Prior to treatment, there were no significant differences in BUN, SCr, or urinary protein between groups (P > 0.05). After 7 days, both groups showed significant improvements in BUN, SCr, and urinary protein levels, with the study group showing greater improvement (P < 0.05). Similarly, neutrophils, CRP, IL-18, and IL-6 levels decreased significantly in both groups, with the study group showing greater reductions (P < 0.05). Regarding oxidative stress markers, SOD levels decreased and MDA levels increased post-treatment in both groups. However, compared to the control group, the study group showed a more pronounced decrease in SOD levels and a more pronounced increase in MDA levels (P < 0.05), findings that are contrary to an expected direct antioxidant effect measured by these specific markers. Adverse reactions were mild in both groups, with the control group having a slightly higher rate (8.16% vs. 4.08%), but no significant differences were observed (P = 0.399). Xuebijing can alleviate AKI after high-voltage electrical burns by inhibiting neutrophils and inflammatory cells. While it improves kidney function and reduces inflammation, its effects on SOD and MDA levels suggest a complex interaction with the oxidative stress system that requires further investigation, as the observed changes in these markers (decreased SOD, increased MDA) in the Xuebijing group were more pronounced than in the control group. It shows potential as an effective treatment option for improving kidney function and reducing inflammation, warranting further clinical application.Clinical trial registration This trial is registered with ClinicalTrials.gov under NCT07026227 (Date of registration: 18/06/2025).

摘要

本研究旨在探讨血必净通过抑制中性粒细胞、炎性细胞来减轻高压电烧伤后急性肾损伤(AKI)的临床效果及其对活性氧(ROS)的潜在影响。纳入了2023年2月至2024年12月在我院住院的96例高压电烧伤后发生AKI的患者。使用计算机生成的随机数字序列将他们随机分为两组:研究组(血必净,n = 48)和对照组(n = 48)。本研究采用开放标签方式进行。在基线(治疗前1小时)和治疗后7天比较中性粒细胞、炎性细胞和ROS水平,以及肾功能和氧化应激因子(超氧化物歧化酶(SOD)、丙二醛(MDA))。记录不良反应。样本量根据既往类似研究确定,这些研究表明在相当的组规模下存在临床显著差异。治疗前,两组间血尿素氮(BUN)、血清肌酐(SCr)或尿蛋白无显著差异(P > 0.05)。7天后,两组的BUN、SCr和尿蛋白水平均显著改善,研究组改善更明显(P < 0.05)。同样,两组的中性粒细胞、C反应蛋白(CRP)、白细胞介素-18(IL-18)和白细胞介素-6(IL-6)水平均显著降低,研究组降低更明显(P < 0.05)。关于氧化应激标志物,两组治疗后SOD水平降低,MDA水平升高。然而,与对照组相比,研究组SOD水平下降更明显,MDA水平升高更明显(P < 0.05),这些结果与通过这些特定标志物测量的预期直接抗氧化作用相反。两组不良反应均较轻,对照组发生率略高(8.16%对4.08%),但未观察到显著差异(P = 0.399)。血必净可通过抑制中性粒细胞和炎性细胞减轻高压电烧伤后的AKI。虽然它改善了肾功能并减轻了炎症,但其对SOD和MDA水平的影响表明与氧化应激系统存在复杂的相互作用,需要进一步研究,因为血必净组中这些标志物的观察变化(SOD降低、MDA升高)比对照组更明显。它显示出作为改善肾功能和减轻炎症的有效治疗选择的潜力,值得进一步临床应用。临床试验注册 本试验已在ClinicalTrials.gov上注册,注册号为NCTO7026227(注册日期:2025年6月18日)。

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