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硫化氢对1型糖尿病大鼠肾脏的保护作用
引用本文:杨锐,刘小粉,马善峰,高琴,李正红,贾强. 硫化氢对1型糖尿病大鼠肾脏的保护作用[J]. 中国应用生理学杂志, 2016, 32(2): 181-184. DOI: 10.13459/j.cnki.cjap.2016.02.023
作者姓名:杨锐  刘小粉  马善峰  高琴  李正红  贾强
作者单位:蚌埠医学院生理学教研室, 安徽 蚌埠 233030
基金项目:国家自然科学基金资助项目(81000074);安徽省高校自然科学研究项目(KJ2013B146,KJ2015B006by,KJ2015A163);蚌埠医学院科研项目(BYKY1312,BYKY1414ZD)
摘    要:目的:观察硫化氢(H2S)对1型糖尿病大鼠肾脏的保护作用及其机制。方法:32只雄性SD大鼠随机分为4组:正常对照(NC)组、糖尿病(DM)组、糖尿病治疗(NaHS+DM)组和NaHS对照(NaHS)组(n=8)。DM组和NaHS+DM组大鼠采用链脲佐菌素(STZ)55 mg/kg腹腔注射诱导1型糖尿病模型。造模成功后,NaHS+DM组和NaHS组采用腹腔注射NaHS溶液56 μmol/kg干预治疗。8周后,测定大鼠24 h尿蛋白含量、肾重指数、空腹血糖、尿素氮、肌酐等指标;HE染色观察肾脏组织形态学变化;测定肾脏组织脂质过氧化物丙二醛(MDA)含量、超氧化物歧化酶(SOD)和Caspase-3的活性;Western blot检测肾脏组织Bcl-2和Bax蛋白表达。结果:与NC组相比,NaHS组各项指标均无显著差异,DM组,24 h尿蛋白含量、肾重指数、空腹血糖、尿素氮和肌酐水平均明显升高;HE染色结果显示肾小球基底膜增厚、系膜基质增多;MDA含量、Caspase-3活性和Bax蛋白表达明显增高;SOD活性和Bcl-2蛋白表达显著降低。与DM组相比,NaHS+DM组肾功能损伤明显减轻,肾脏组织形态学变化明显改善,MDA含量、Caspase-3活性和Bax蛋白表达明显下降,SOD活性和Bcl-2蛋白表达显著增高。结论:H2S对1型糖尿病大鼠肾脏具有保护作用,其机制可能与抑制氧化应激和细胞凋亡有关。

关 键 词:硫化氢  糖尿病  大鼠  肾功能  氧化应激  细胞凋亡  
收稿时间:2015-08-13

Protective effect of hydrogen sulfide on kidneys of type 1 diabetic rats
YANG Rui,LIU Xiao-fen,MA Shan-feng,GAO Qin,LI Zheng-hong,JIA Qiang. Protective effect of hydrogen sulfide on kidneys of type 1 diabetic rats[J]. Chinese journal of applied physiology, 2016, 32(2): 181-184. DOI: 10.13459/j.cnki.cjap.2016.02.023
Authors:YANG Rui  LIU Xiao-fen  MA Shan-feng  GAO Qin  LI Zheng-hong  JIA Qiang
Affiliation:Department of Physiology, Bengbu Medical College, Bengbu 233030, China
Abstract:Objective: To explore the protective effects of hydrogen sulfide (H2S) on kidneys of type 1 diabetic rats and its underlying mechanism. Methods: Thirty-two male SD rats were randomly divided into four groups:normal control (NC) group, diabetes mellitus (DM) group, DM treatment (NaHS+DM) group and NaHS control (NaHS) group. The rats from DM group and NaHS+DM group were injected intraperitoneally with Streptozotocin 55 mg/kg to induce type 1 diabetes mellitus (n=8). After modeling, rats in NaHS+DM group and NaHS group were intraperitoneally injected with NaHS solution at the dosage of 56 μmol/kg. After 8 weeks, urinary protein content was detected in urine samples collected for 24 h. and the ratio of kidney weight/body weight (renal index) was determined in isolated kidneys. Besides, the levels of fasting blood glucose (FBG), blood urea nitrogen (BUN) and serum creatinine (Scr) were measured biochemically. The morphological changes of renal tissue were observed by HE staining. The content of malondialdehyde (MDA), the activities of superoxide dismutase (SOD) and Caspase-3 in renal tissue were determined by spectrophotometry. The protein expression levels of Bcl-2 and Bax in renal tissue were detected using Western blot. Results: There was no significant difference in the respective measured indexes in rats between NC group and NaHS group. However, in DM group, the levels of 24 h urinary protein, FBG, BUN, Scr and renal index were increased significantly; HE staining showed that the basement membrane was thickened and the amount of glomerular mesangial matrix was increased; MDA content, Caspase-3 activity and Bax expression levels were increased, while SOD activity and Bcl-2 expression were decreased. Compared with those in DM group, the morphological changes of renal tissue and its function were improved; MDA content, Caspase-3 activity and Bax expression were decreased significantly, while SOD activity and Bcl-2 expression were increased obviously in NaHS+DM group. Conclusion: H2S can protect the kidneys of type 1 diabetic rats, which is related to suppressing oxidative stress and cell apoptosis.
Keywords:hydrogen sulfide  diabetes mellitus  rat  renal function  oxidative stress  cell apoptosis  
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