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腺苷酸环化激酶-雷帕霉素靶蛋白信号通路参与小鼠急性肾损伤的机制研究
引用本文:查志刚,陈全景. 腺苷酸环化激酶-雷帕霉素靶蛋白信号通路参与小鼠急性肾损伤的机制研究[J]. 国际泌尿系统杂志, 2021, 41(2): 204-208. DOI: 10.3760/cma.j.cn431460-20191031-00003
作者姓名:查志刚  陈全景
作者单位:湖北医药学院附属东风医院儿科,十堰 442000
摘    要:目的 探讨腺苷酸环化激酶(AMPK)-雷帕霉素靶蛋白(mTOR)信号通路参与小鼠急性肾损伤的机制.方法 将健康雄性C57BL/6小鼠随机分为对照组、模型组及SB2111组,每组各10只.模型组与SB2111组小鼠采用脂多糖(LPS)建立急性肾损伤模型,对照组以等剂量的生理盐水代替.SB2111组另外给予经腹腔右侧注射2...

关 键 词:腺苷酸环化酶  雷帕霉素靶蛋白  模型  动物  小鼠  急性肾损伤

Mechanism of AMPR-mTOR signaling pathway involved in acute kidney injury in mice
Zha Zhigang,Chen Quanjing. Mechanism of AMPR-mTOR signaling pathway involved in acute kidney injury in mice[J]. International Journal of Urology and Nephrology, 2021, 41(2): 204-208. DOI: 10.3760/cma.j.cn431460-20191031-00003
Authors:Zha Zhigang  Chen Quanjing
Affiliation:(Department of Pediatrics,Dongfeng Hospital,Hubei University of Medicine,Shiyan 442000,China)
Abstract:Objective To investigate the mechanism of AMP-activated protein kinase(AMPK)-mammalian target of rapamycin(mTOR)signaling pathway involved in acute kidney injury in mice.Methods Thirty cases of healthy male C57BL/6 mice were divided into three groups-control group,model group and SB2111 group,with 10 mice in each group.Both the model group and the SB2111 group were treated with lipopolysaccharide(LPS)to establish acute kidney injury model,the control group were replaced with equal dose of normal saline,the SB2111 group were treated with 2 mL of AMPK blocker SB2111.The general condition and pathological characteristics of the mice were observed and recorded,and renal function were detected.Results The body weight of the model group and the SB2111 group were significantly lower than those of the control group(P<0.05),and the kidney of the model group were significantly higher than the control group(P<0.05)that there were no significant difference compared between the SB2111 group and the control group(P>0.05).After the experiment,the 24 h urine protein,serum creatinine and urea nitrogen in the model group and SB2111 group were higher than the control group,and the SB2111 group were lower than the model group that compared the difference were statistically significant(P<0.05).The renal tubular epithelial cells in the control group were rich in cytoplasm,the glomeruli and renal tubules in the renal tissues were normal,the glomerular congestion and tubular formation in the model group,the glomerular congestion in the SB2111 group,and the proximal koji,tubular epithelial cells were slightly swollen with small amount of inflammatory cell infiltration.The relative expression levels of TNF-α,TGF-β1,AMPK and mTOR in the model group and SB2111 group were significantly higher than those in the control group,and the SB2111 group were lower than the model group that compared the difference were statistically significant(P<0.05).Conclusions AMPK-mTOR signaling pathway are activated in acute kidney injury in mice.Inhibition of AMPK-mTOR signaling pathway can inhibit the expression of TNF-αand TGF-β1 and promote the recovery of renal function in mice.
Keywords:Adenylate Cyclase  Rapamycin Target Protein  Models,Animal  Mice  Acute Kidney Injury
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