Department of Urology, The Central Hospital of Wuhan, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, People's Republic of China.
Hemodialysis Center, Wuhan University of Science and Technology Hospital, Wuhan, People's Republic of China.
Int Urol Nephrol. 2023 Oct;55(10):2599-2610. doi: 10.1007/s11255-023-03494-4. Epub 2023 Mar 19.
To investigate the effect of grape seed-derived proanthocyanidin B2 (GSPB2) pretreatment on acute renal ischemia-reperfusion injury model of mice.
50 mice were divided into 5 groups: Sham group: mice were treated with right nephrectomy. GSPB2 group: GSPB2 was injected intraperitoneally 45 min before right nephrectomy. IRI group: right kidney was resected and the left renal arteriovenous vessel was blocked for 45 min. GSPB2 + IRI group: GSPB2 was intraperitoneally injected 45 min before IRI established. GSPB2 + BRU + IRI group: GSPB2 and brusatol (BRU) were injected intraperitoneally 45 min before IRI established. Creatinine and urea nitrogen of mice were detected, and the kidney morphology and pathological changes of each group were detected by HE staining, PAS staining and transmission electron microscopy. Expressions of Nrf2, HO-1, GRP78, CHOP, and cleaved-caspase3 were detected by immunofluorescence staining and western blotting.
Morphology and mitochondrial damages of kidney in GSPB2 + IRI group were significantly alleviated than those in IRI group. Expression levels of Nrf2 and HO-1 were significantly higher in GSPB2 + IRI group than those in IRI group. Expression levels of GRP78, CHOP and cleaved-caspase3 were significantly lower in GSPB2 + IRI group than those in IRI group. However, compared to GSPB2 + IRI group, protective effects of GSPB2 pretreatment were weakened in GSPB2 + BRU + IRI group.
GSPB2 pretreatment could alleviate oxidative stress damage and reduce apoptosis of renal tubular epithelial cells, which might be related to activating the antioxidant system, up-regulating the expression of Nrf2 and HO-1, inhibiting the expressions of GRP78, CHOP and cleaved-caspase3. However, the protective effect could be reversed by brusatol.
探讨葡萄籽原花青素 B2(GSPB2)预处理对小鼠急性肾缺血再灌注损伤模型的影响。
将 50 只小鼠分为 5 组:假手术组:小鼠行右肾切除术。GSPB2 组:右肾切除前 45 min 腹腔注射 GSPB2。IRI 组:切除右肾,阻断左肾动静脉 45 min。GSPB2+IRI 组:在建立 IRI 前 45 min 腹腔内注射 GSPB2。GSPB2+BRU+IRI 组:在建立 IRI 前 45 min 腹腔内注射 GSPB2 和溴夫定(BRU)。检测小鼠血肌酐和血尿素氮,HE 染色、PAS 染色和透射电镜观察各组肾脏形态学和病理变化。免疫荧光染色和 Western blot 检测 Nrf2、HO-1、GRP78、CHOP 和 cleaved-caspase3 的表达。
与 IRI 组相比,GSPB2+IRI 组肾脏形态和线粒体损伤明显减轻。GSPB2+IRI 组 Nrf2 和 HO-1 的表达水平明显高于 IRI 组。GSPB2+IRI 组 GRP78、CHOP 和 cleaved-caspase3 的表达水平明显低于 IRI 组。然而,与 GSPB2+IRI 组相比,GSPB2+BRU+IRI 组 GSPB2 预处理的保护作用减弱。
GSPB2 预处理可减轻氧化应激损伤,减少肾小管上皮细胞凋亡,其机制可能与激活抗氧化系统、上调 Nrf2 和 HO-1 的表达、抑制 GRP78、CHOP 和 cleaved-caspase3 的表达有关。然而,这种保护作用可被溴夫定逆转。