透皮GFR能够在无肾小管损伤的肝硬化小鼠模型中早期检测功能性急性肾损伤。

IF 3 Q1 UROLOGY & NEPHROLOGY
Kidney360 Pub Date : 2025-10-08 DOI:10.34067/KID.0000001007
Xuegang Zhao, Xin Sui, Huimin Yi, Jianrong Liu, Yufeng He, Yangbin Li, Lixin Tang, Yunshan Zou, Haijin Lyu
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引用次数: 0

摘要

背景:AKI是终末期肝病患者中一种常见的并发症,与显著的死亡率相关。目前的诊断标准主要依赖于血清肌酐水平,而血清肌酐水平可能受到肝硬化患者中常见的肌肉量减少的影响,从而延迟了对肾脏损害的识别。本研究旨在评价经皮肾小球滤过率(tGFR)测定在AKI小鼠肝硬化模型中早期诊断肾功能障碍的作用。方法:通过12周灌胃50%四氯化碳(CCl4, 1 mL/kg),然后单次腹腔注射脂多糖(LPS),建立肝硬化相关AKI (cAKI)小鼠模型。通过经皮肾小球滤过率(tGFR)测量评估肾功能,并与常规指标(包括血清肌酐和血尿素氮(BUN)水平)进行比较。结果:在小鼠cAKI模型诱导后,小鼠接受单次静脉注射异硫氰酸荧光素(FITC)偶联sininistrin (75 mg/kg)。使用附着在皮肤上的小型化传感器,每2秒连续监测一次fitc - sininistrin荧光强度,持续1.5至2小时。采用双室药代动力学模型,基于相对荧光强度(RFI)曲线计算经皮肾小球滤过率(tGFR)。分别于LPS给药后2、4、8、12和24小时测定血清尿素氮(BUN)和肌酐(CREA)水平。组织学分析显示cAKI未引起明显的肾小管损伤。值得注意的是,tGFR检测到早在lps后2小时肾小球滤过明显减少(0.54±0.207 vs 1.06±0.273 μL/min/100 g),而BUN水平直到4小时才显著升高(33.94±3.683 vs 18.7±2.414mmol/L)。血清肌酐和BUN/CREA比值在观察期内无明显变化。结论:与肌酐和bun标准相比,经皮肾小球滤过率在肝硬化相关AKI肾功能损害的早期检测中表现出更高的敏感性,突出了其潜在的临床应用价值,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transdermal GFR Enables Early Detection of Functional Acute Kidney Injury in a Cirrhotic Mouse Model Without Tubular Injury.

Background: AKI is a common complication associated with significant mortality in patients with end-stage liver disease. Current diagnostic criteria primarily rely on serum creatinine levels, which may be influenced by reduced muscle mass commonly observed in cirrhotic patients, thereby delaying the recognition of renal impairment. This study aims to evaluate the efficacy of transdermal glomerular filtration rate (tGFR) measurement for the early diagnosis of renal dysfunction in a AKI murine model of cirrhosis.

Methods: A murine model of cirrhosis-associated AKI (cAKI) was established through a 12-week regimen of intragastric administration of 50% carbon tetrachloride (CCl4, 1 mL/kg), followed by a single intraperitoneal injection of lipopolysaccharide (LPS). Renal function was evaluated using transdermal glomerular filtration rate (tGFR) measurement and compared with conventional markers, including serum creatinine and blood urea nitrogen (BUN) levels.

Results: Following the induction of the murine model of cAKI, mice received a single intravenous dose of fluorescein-isothiocyanate (FITC)-conjugated sinistrin (75 mg/kg). FITC-sinistrin fluorescence intensity was continuously monitored every 2 seconds for 1.5 to 2 hours using a skin-attached miniaturized sensor. The transdermal glomerular filtration rate (tGFR) was calculated based on a relative fluorescence intensity (RFI) curve using a two-compartment pharmacokinetic model. Serum blood urea nitrogen (BUN) and creatinine (CREA) levels were measured at 2, 4, 8, 12, and 24 hours after LPS administration. Histological analysis revealed that cAKI did not induce significant tubular injury. Notably, tGFR detected a significant reduction in glomerular filtration as early as 2 hours post-LPS ( 0.54± 0.207 vs. 1.06 ± 0.273 μL/min/100 g), whereas BUN levels did not rise significantly until 4 hours (33.94 ± 3.683 vs. 18.7 ± 2.414mmol/L). Serum creatinine and the BUN/CREA ratio showed no significant changes throughout the observation period.

Conclusions: Transdermal glomerular filtration rate demonstrates superior sensitivity compared to creatinine- and BUN-based criteria for the early detection of renal impairment in cirrhosis-associated AKI, highlighting its potential clinical utility and warranting further investigation.

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来源期刊
Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
CiteScore
3.90
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