Qian Lichao, Ren Shuai, Xu Zhongchi, Zheng Yawei, Wu Lihua, Yang Ying, Wang Yixuan, Li Jie, Yan Shihai, Fang Zhuyuan
Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Front Pharmacol. 2021 Jun 7;12:667433. doi: 10.3389/fphar.2021.667433. eCollection 2021.
Protection against hypoxia injury is an important therapeutic strategy for treating hypertensive nephropathy. In this study, the effects of Qian Yang Yu Yin granule (QYYY) on spontaneously hypertensive rats fed with high salt diet and HEK293T cells exposed to hypoxia were investigated. After eight weeks' treatment of QYYY, blood pressure, serum creatinine, serum cystatin C, blood urea nitrogen, urinary β2-microglobulin, urinary N-acetyl-β-glucosaminidase, and urinary microalbumin were assessed. The changes of hypoxia-inducible factor-1α (HIF-1α), pyruvate kinase M2 (PKM2), glucose transport 1 (GLUT1), lactate dehydrogenase A (LDH-A), connective tissue growth factor (CTGF), transforming growth factor-β1 (TGF-β1), ATP, lactate, pyruvate, and pathology were also assessed . HEK293T cells pre-treated with QYYY and/or HIF-1α over expressing cells were cultured in a three gas hypoxic incubator chamber (5% CO, 1% O, 94% N) for 12 h and then the expressions of HIF-1α, PKM2, GLUT1, LDH-A, CTGF, TGF-β1, ATP, lactate, and pyruvate were detected. Our results showed that QYYY promoted the indicators of renal inflammation and fibrosis mediated by HIF-1α/PKM2 positive feedback loop and . Our findings indicated that QYYY treated hypertensive nephropathy by regulating metabolic reprogramming mediated by HIF-1α/PKM2 positive feedback loop.
预防缺氧损伤是治疗高血压肾病的重要治疗策略。本研究考察了潜阳育阴颗粒(QYYY)对高盐饮食喂养的自发性高血压大鼠和缺氧处理的HEK293T细胞的影响。用QYYY治疗八周后,评估血压、血清肌酐、血清胱抑素C、血尿素氮、尿β2-微球蛋白、尿N-乙酰-β-葡萄糖苷酶和尿微量白蛋白。还评估了缺氧诱导因子-1α(HIF-1α)、丙酮酸激酶M2(PKM2)、葡萄糖转运蛋白1(GLUT1)、乳酸脱氢酶A(LDH-A)、结缔组织生长因子(CTGF)、转化生长因子-β1(TGF-β1)、ATP、乳酸、丙酮酸的变化以及病理学变化。将用QYYY预处理的HEK293T细胞和/或过表达HIF-1α的细胞在三气缺氧培养箱(5%CO₂、1%O₂、94%N₂)中培养12小时,然后检测HIF-1α、PKM2、GLUT1、LDH-A、CTGF、TGF-β1、ATP、乳酸和丙酮酸的表达。我们的结果表明,QYYY促进了由HIF-1α/PKM2正反馈环介导的肾脏炎症和纤维化指标。我们的研究结果表明,QYYY通过调节由HIF-1α/PKM2正反馈环介导的代谢重编程来治疗高血压肾病。