Wang Zhi-Shun, Zhou Hai-Hong, Han Qi, Guo Yong-Lian, Li Zhong-Yuan
PhD, Department of Urology, The Central Hospital of Wuhan , Tongji Medical College , Huazhong University of Science and Technology , Wuhan , China . Conception and design of the study, acquisition and analysis of data, manuscript writing.
PhD, Department of Urology, The Central Hospital of Wuhan , Tongji Medical College , Huazhong University of Science and Technology , Wuhan , China . Conception and design of the study, acquisition and analysis of data.
Acta Cir Bras. 2020 Sep 4;35(8):e202000802. doi: 10.1590/s0102-865020200080000002.
To investigate the effects of grape seed proanthocyanidin B2 (GSPB2) preconditioning on oxidative stress and apoptosis of renal tubular epithelial cells in mice after renal ischemia-reperfusion (RIR).
Forty male ICR mice were randomly divided into 4 groups: Group A: mice were treated with right nephrectomy. Group B: right kidney was resected and the left renal vessel was clamped for 45 minutes. Group C: mice were intraperitoneally injected with GSPB2 before RIR established. Group D: mice were intraperitoneally injected with GSPB2 plus brusatol before RIR established. Creatinine and urea nitrogen of mice were determined. Pathological and morphological changes of kidney were checked. Expressions of Nrf-2, HO-1, cleaved-caspase3 were detected by Western-blot.
Compared to Group B, morphology and pathological damages of renal tissue were less serious in Group C. Western-blot showed that expressions of Nrf-2 and HO-1 in Group C were obviously higher than those in Group B. The expression of cleaved-caspase3 in Group C was significantly lower than that in Group B.
GSPB2 preconditioning could attenuate renal oxidative stress injury and renal tubular epithelial cell apoptosis by up-regulating expressions of Nrf-2 and HO-1 and down-regulating the expression of cleaved-caspase-3, but the protective effect could be reversed by brusatol.
探讨葡萄籽原花青素B2(GSPB2)预处理对肾缺血再灌注(RIR)后小鼠肾小管上皮细胞氧化应激及凋亡的影响。
将40只雄性ICR小鼠随机分为4组:A组:行右肾切除术;B组:切除右肾并夹闭左肾血管45分钟;C组:在建立RIR模型前腹腔注射GSPB2;D组:在建立RIR模型前腹腔注射GSPB2加布罗索龙。检测小鼠肌酐和尿素氮水平。检查肾脏的病理和形态学变化。通过蛋白质免疫印迹法检测Nrf-2、HO-1、裂解型半胱天冬酶3的表达。
与B组相比,C组肾组织的形态和病理损伤较轻。蛋白质免疫印迹法显示,C组Nrf-2和HO-1的表达明显高于B组。C组裂解型半胱天冬酶3的表达明显低于B组。
GSPB2预处理可通过上调Nrf-2和HO-1的表达、下调裂解型半胱天冬酶-3的表达减轻肾脏氧化应激损伤和肾小管上皮细胞凋亡,但布罗索龙可逆转其保护作用。