Jiang Jun, Yin Jiangning, Liu Xiang, Wang Huajun, Lu Guoyuan
School of Pharmacy, Jiangsu University, No. 301 Xuefu Road, Zhenjiang, Jiangsu 212013, China.
Affiliated Hospital of Jiangsu University, No. 438 Jiefang Road, Zhenjiang, Jiangsu 212001, China.
Evid Based Complement Alternat Med. 2018 Aug 23;2018:1741924. doi: 10.1155/2018/1741924. eCollection 2018.
Podocytes injury was a crucial factor resulting in diabetic nephropathy (DN). Erzhi formula extract (EZF) was a clinical effective Chinese medicine on DN, but its mechanism was unclear. In this study, the main compounds of EZF and their pharmacokinetics in rat were detected by HPLC-MS/MS. And then, blood glucose, urine protein, renal index, renal microstructural (HE/PAS staining), inflammatory factors (IL-, TNF-, IL-6), and protein/mRNA expression related to the function of podocyte (CD2AP and Podocin) in DN rats were investigated after the oral administration of EZF. The concentrations of specnuezhenide and wedelolactone in rat kidney were 7.19 and 0.057 mg/kg, respectively. The T of specnuezhenide and wedelolactone were 2.0 and 1.50 h, respectively. Their C were, respectively, 30.24 ± 2.68 and 6.39 ± 0.05 g/L. Their AUC were 123.30 ± 2.68 and 16.56 ± 0.98 g/L⁎h, respectively. Compared with the model group, the blood glucose and the 24-hour urinary protein were significantly decreased (P < 0.05) after 16 weeks' treatment of EZF. The expressions of Podocin and CD2AP protein/mRNA were increased (P < 0. 05). The deteriorate of glomerular morphology was alleviated under the treatment of EZF. EZF prominently decreased the levels of inflammatory factors (P < 0.05). MDA was significantly decreased (P < 0.05) with the significant increase of SOD activity (P < 0.05) in EZF groups. All the results proved that EZF repaired glomerular mesangial matrix, protected renal tubule, and improved renal function in DN rats by upregulating the expression of Podocin and CD2AP protein/mRNA in podocytes.
足细胞损伤是导致糖尿病肾病(DN)的关键因素。二至丸提取物(EZF)是一种治疗DN的临床有效中药,但其作用机制尚不清楚。本研究采用HPLC-MS/MS法检测EZF的主要成分及其在大鼠体内的药代动力学。然后,对DN大鼠口服EZF后,检测其血糖、尿蛋白、肾指数、肾脏微观结构(HE/PAS染色)、炎症因子(IL-、TNF-、IL-6)以及与足细胞功能相关的蛋白/ mRNA表达(CD2AP和Podocin)。大鼠肾脏中specnuezhenide和wedelolactone的浓度分别为7.19和0.057 mg/kg。specnuezhenide和wedelolactone的T分别为2.0和1.50 h。其C分别为30.24±2.68和6.39±0.05 g/L。其AUC分别为123.30±2.68和16.56±0.98 g/L⁎h。与模型组相比,EZF治疗16周后,血糖和24小时尿蛋白显著降低(P<0.05)。Podocin和CD2AP蛋白/ mRNA的表达增加(P<0.05)。EZF治疗可减轻肾小球形态的恶化。EZF显著降低炎症因子水平(P<0.05)。EZF组MDA显著降低(P<0.05),SOD活性显著升高(P<0.05)。所有结果证明,EZF通过上调足细胞中Podocin和CD2AP蛋白/ mRNA的表达,修复肾小球系膜基质,保护肾小管,改善DN大鼠的肾功能。