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外源性硫化氢抑制TLR2和TLR4表达并减轻大鼠肾脏缺血再灌注损伤
引用本文:张文文,闫琰,董毅玲,覃志成. 外源性硫化氢抑制TLR2和TLR4表达并减轻大鼠肾脏缺血再灌注损伤[J]. 中华肾病研究电子杂志, 2022, 11(2): 61-66. DOI: 10.3877/cma.j.issn.2095-3216.2022.02.001
作者姓名:张文文  闫琰  董毅玲  覃志成
作者单位:1. 030012 太原,山西医科大学第五临床医学院肾内科、山西省肾脏病重点实验室
基金项目:山西省"136"兴医工程专项基金(SZ2019011)
摘    要:目的观察外源性硫化氢(H2S)供体硫氢化钠(NaHS)能否抑制Toll样受体2(TLR2)和Toll样受体4(TLR4)表达、减轻大鼠肾脏缺血再灌注损伤(IRI)。 方法24只6~8周龄雄性SD大鼠随机分为3组:假手术(Sham)组、肾脏缺血再灌注(I/R)组、NaHS+I/R组。采用右肾切除联合左肾动脉夹闭45 min后再灌注24 h的方法诱导肾IRI。夹闭左肾动脉前,NaHS+I/R组给予NaHS(300 nmol/min)连续输注10 min,Sham组和I/R组则给予等体积生理盐水。分别留取各组腹主动脉血及肾组织标本。Western印迹法检测肾组织TLR2、TLR4蛋白的表达;免疫组织化学法检测肾组织白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)的表达;比色法检测血尿素氮(BUN)、血肌酐(Scr)。HE染色观察肾脏组织学改变;TUNEL法检测肾组织细胞凋亡。 结果与Sham组比较,I/R组的TLR2、TLR4、IL-6、TNF-α表达均增加(P<0.05),BUN、Scr亦明显升高(P<0.05),肾小管上皮损伤评分较高(P<0.05),肾组织凋亡细胞增加(P<0.05)。与I/R组比较,NaHS+I/R组的TLR2、TLR4、IL-6、TNF-α表达均减少(P<0.05),BUN、Scr亦明显下降(P<0.05),肾小管上皮损伤评分较低(P<0.05),肾组织凋亡细胞减少(P<0.05)。 结论外源性H2S可以抑制TLR2、TLR4途径,减少炎症因子释放及细胞凋亡,减轻大鼠肾脏IRI。

关 键 词:硫化氢  肾脏  缺血再灌注损伤  Toll样受体  
收稿时间:2021-09-15

Exogenous hydrogen sulfide inhibited TLR2 and TLR4 expression and alleviated the renal ischemia-reperfusion injury in rats
Wenwen Zhang,Yan Yan,Yiling Dong,Zhicheng Tan. Exogenous hydrogen sulfide inhibited TLR2 and TLR4 expression and alleviated the renal ischemia-reperfusion injury in rats[J]. Chinese Journal of kidney disease investigation (Electronic Edition), 2022, 11(2): 61-66. DOI: 10.3877/cma.j.issn.2095-3216.2022.02.001
Authors:Wenwen Zhang  Yan Yan  Yiling Dong  Zhicheng Tan
Affiliation:1. Department of Nephrology, Fifth Clinical Medical College of Shanxi Medical University, Shanxi Provincial Key Laboratory of Nephrology, Taiyuan 030012, Shanxi Province, China
Abstract:ObjectiveTo observe whether exogenous hydrogen sulfide (H2S) donor sodium hydrosulfide (NaHS) can alleviate renal ischemia-reperfusion injury (IRI) in rats by inhibiting the expression of Toll-like receptor 2 (TLR2) and Toll-like receptor 4 (TLR4). MethodsTwenty-four male SD rats aged 6-8 weeks were randomly divided into 3 groups: sham group (renal sham operation), I/R group (renal ischemia-reperfusion), and NaHS+ I/R group. Renal IRI was induced by right nephrectomy combined with left renal artery clipping for 45 minutes followed by 24 hours of reperfusion. Before the left renal artery clipping, the NaHS+ I/R group was given a continuous infusion of NaHS (300 nmol/min) for 10 minutes, while the sham group and I/R group were given an equal volume of normal saline. Abdominal aortic blood and kidney tissue samples were collected from each group. The expression of TLR2 and TLR4 protein in renal tissue was detected by western blotting. The expression of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) in renal tissue was detected by immunohistochemistry. Blood urea nitrogen (BUN) and serum creatinine (Scr) were detected by colorimetry. HE staining was used to observe renal histological changes, and TUNEL method to detect renal tissue apoptosis. ResultsCompared with the sham group, the I/R group showed more expression of TLR2, TLR4, IL-6 and TNF-α (P<0.05), higher levels of BUN and Scr (P<0.05), higher scores of the renal tubular injury (P<0.05), and more apoptotic cells in the renal tissue (P<0.05). Compared with the I/R group, the NaHS+ I/R group showed less expression of TLR2, TLR4, IL-6 and TNF-α (P<0.05), lower levels of BUN and Scr (P<0.05), lower scores of the renal tubular injury (P<0.05), and less apoptotic cells in the renal tissue (P<0.05). ConclusionExogenous H2S inhibited the expression of TLR2 and TLR4, reduced the release of inflammatory factors and apoptosis, and alleviated the renal IRI in rats.
Keywords:Hydrogen sulfide  Kidney  Ischemia-reperfusion injury  Toll-like receptor  
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