Zhan Juan, Wang Kun, Zhang Conghui, Zhang Chunxiu, Li Yueqiang, Zhang Ying, Chang Xiaoyan, Zhou Qiaodan, Yao Ying, Liu Yanyan, Xu Gang
Department of Nephrology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Ave, Wuhan 430030, Hubei, China.
Int J Mol Sci. 2016 Sep 29;17(10):1647. doi: 10.3390/ijms17101647.
Grape seed proanthocyanindin extract (GSPE) is a polyphenolic bioflavonoid derived from grape seeds and has been widely studied for its potent antioxidant, anti-inflammatory and antitumor activities. HMGB1 is a newly discovered danger-associated molecular pattern (DAMP) that has potent proinflammatory effects once released by necrotic cells. However, the effect of GSPE on the HMGB1, and the relationship of those two with acute kidney injury and chronic kidney fibrosis are unknown. This study aimed to investigate the impact of GSPE on acute kidney injury and chronic fibrosis. C57bl/6 mice were subjected to bilateral ischemia/reperfusion (I/R) and unilateral I/R with or without GSPE administration. After bilateral I/R, mice administered GSPE had a marked improvement in renal function (BUN and Cr), decreased pathological damage and reduced inflammation. In unilateral I/R, mice subjected GSPE showed reduced tubulointerstitial fibrosis and decreased inflammatory reaction. The renoprotection of GSPE on both models was associated with the inhibition of HMGB1 nucleocytoplasmic shuttling and release, which can amplify the inflammation through binding to its downstream receptor TLR4 and facilitated P65 transcription. Thus, we have reason to believe that GSPE could be a good alternative therapy for the prevention and treatment of IR-induced renal injury and fibrosis in clinical practice.
葡萄籽原花青素提取物(GSPE)是一种源自葡萄籽的多酚类生物黄酮,因其具有强大的抗氧化、抗炎和抗肿瘤活性而受到广泛研究。HMGB1是一种新发现的与危险相关的分子模式(DAMP),一旦由坏死细胞释放,就具有强大的促炎作用。然而,GSPE对HMGB1的影响以及二者与急性肾损伤和慢性肾纤维化的关系尚不清楚。本研究旨在探讨GSPE对急性肾损伤和慢性纤维化的影响。对C57bl/6小鼠进行双侧缺血/再灌注(I/R)和单侧I/R,并给予或不给予GSPE。双侧I/R后,给予GSPE的小鼠肾功能(血尿素氮和肌酐)有明显改善,病理损伤减轻,炎症反应减轻。在单侧I/R中,给予GSPE的小鼠肾小管间质纤维化减轻,炎症反应减轻。GSPE对两种模型的肾脏保护作用与抑制HMGB1的核质穿梭和释放有关,HMGB1可通过与其下游受体TLR4结合并促进P65转录来放大炎症。因此,我们有理由相信,在临床实践中,GSPE可能是预防和治疗IR诱导的肾损伤和纤维化的一种良好替代疗法。