Zhang Xiuli, Guan Tingwen, Yang Boxuan, Chi Zhihong, Wan Qijun, Gu Harvest F
Department of Nephrology, The Second People's Hospital, The First Affiliated Hospital of Shenzhen University Shenzhen 518000, Guangdong, P. R. China.
Department of Pathophysiology, China Medical University Shenyang 110001, Liaoning, P. R. China.
Am J Transl Res. 2019 Feb 15;11(2):669-682. eCollection 2019.
Berberine (BBR), derived from Huanglian (), is a traditional Chinese herbal medicine. In the current study, we investigated the effects of BBR in high glucose (HG) and hypoxia-induced apoptosis with normal rat renal tubular epithelial (NRK-52E) and human kidney proximal tubular cells (HK-2) and further explored the underlying molecular mechanism of hypoxia-inducible factor 1α (HIF-1α) in diabetic kidney disease (DKD). Apoptosis in NRK-52E and HK-2 cells induced by HG (30 mM)/hypoxia and anti-apoptosis with BBR pretreatment (30 μM) were analyzed by using the terminal uridine nick 3' end labeling method. Activities of apoptotic proteins and anti-apoptotic factor at mRNA and protein levels were determined with real-time RT-PCR and Western blot. HIF-1α action in the apoptosis with BBR pretreatment or siRNA interfere was investigated with flow-cytometry and Western blot. Up-regulation of apoptotic proteins (Bax cytochrome C, caspase 9 and caspase 3) and down-regulation of anti-apoptotic factor Bcl-xL were accompanied with HG/Hypoxia-induced apoptosis in NRK-52E and HK-2 cells but all reversals were found after BBR pretreatment. Activity of HIF-1α was induced under HG/Hypoxia conditions and up-regulated with BBR pretreatment. Furthermore, knockdown of HIF-1α via siRNA significantly removed the anti-apoptosis effects of BBR, while the BBR-mediated HIF-1α activity was suppressed by the pharmacological inhibition of Akt. The present study thereby provided evidence that BBR protected renal tubular epithelial cells from hypoxia/HG-induced apoptosis through activation of HIF-1α in the PI3K/Akt signal pathway and suggested that BBR could be a potential drug in DKD.
黄连素(BBR)源自黄连,是一种传统的中草药。在本研究中,我们研究了黄连素对高糖(HG)和缺氧诱导的正常大鼠肾小管上皮细胞(NRK-52E)和人肾近端小管细胞(HK-2)凋亡的影响,并进一步探讨了缺氧诱导因子1α(HIF-1α)在糖尿病肾病(DKD)中的潜在分子机制。采用末端脱氧核苷酸转移酶介导的缺口末端标记法分析HG(30 mM)/缺氧诱导的NRK-52E和HK-2细胞凋亡以及黄连素预处理(30 μM)的抗凋亡作用。用实时逆转录聚合酶链反应和蛋白质免疫印迹法测定凋亡蛋白和抗凋亡因子在mRNA和蛋白质水平的活性。通过流式细胞术和蛋白质免疫印迹法研究黄连素预处理或小干扰RNA(siRNA)干扰时HIF-1α在细胞凋亡中的作用。凋亡蛋白(Bax、细胞色素C、半胱天冬酶9和半胱天冬酶3)上调以及抗凋亡因子Bcl-xL下调与HG/缺氧诱导的NRK-52E和HK-2细胞凋亡相关,但黄连素预处理后均出现逆转。HG/缺氧条件下诱导HIF-1α活性,黄连素预处理使其上调。此外,通过siRNA敲低HIF-1α可显著消除黄连素的抗凋亡作用,而PI3K/Akt信号通路的药理学抑制可抑制黄连素介导的HIF-1α活性。本研究因此提供了证据,表明黄连素通过PI3K/Akt信号通路激活HIF-1α保护肾小管上皮细胞免受缺氧/HG诱导的凋亡,并提示黄连素可能是DKD的一种潜在药物。