Department of Nephrology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong Province, 250012, People's Republic of China.
Drug Des Devel Ther. 2021 Feb 16;15:589-600. doi: 10.2147/DDDT.S294009. eCollection 2021.
Diabetic Nephropathy remains a major cause of morbidity and mortality in patients suffering from renal dysfunction. This study accessed the nephroprotective role of Adropinin against streptozotocin (STZ) induced diabetic nephropathy in rats and scrutinizes the possible mechanism of action.
STZ (45 mg/kg) dose was used for inducing diabetic nephropathy (DN) and rats were divided into different groups and received the dose-dependent treatment of Adropinin. Blood glucose level, body weight, tissue weight, antioxidant, renal, hepatic parameters, and cytokines were determined. At the end of the experimental study, renal histopathology was performed.
Adropinin significantly (P<0.001) boosted plasma insulin levels and reduced the blood glucose level. Adropinin considerably increased body weight and reduced kidney weight and kidney hypertrophy. Adropinin significantly (P<0.001) reduced urine outflow, microalbumin, total protein, blood urea nitrogen (BUN), uric acid and increased the creatinine, creatinine clearance. Adropinin significantly (P<0.001) reduced the indole sulfate level in the serum, kidney and reduced in the urine. Adropinin significantly (P<0.001) reduced the total cholesterol, triglyceride, low-density lipoprotein (LDL), very-low-density lipoprotein (VLDL) and increased the level of high-density lipoprotein (HDL). Adropinin significantly (P<0.001) increased the level of antioxidant enzymes such as glutathione (GSH), superoxide dismutase (SOD), catalase (CAT) and reduced the level of malonaldehyde (MDA), 8-hydroxy-2' -deoxyguanosine (8-OHdG). Adropinin significantly (P<0.001) reduced the level of interleukin-1β (IL-1β), interleukin-6 (IL-6), transforming growth factor beta (TGF-β) and increased the level of interleukin-10 (IL-10), respectively. Adropinin treatment showed improvement in renal histopathology.
We can say that Adropinin showed the nephroprotective effect against the STZ-induced diabetic nephropathy rats via inflammatory and antioxidant pathway.
糖尿病肾病仍然是肾功能障碍患者发病率和死亡率的主要原因。本研究评估了 Adropinin 对链脲佐菌素(STZ)诱导的糖尿病肾病大鼠的肾保护作用,并探讨了其可能的作用机制。
使用 STZ(45mg/kg)剂量诱导糖尿病肾病(DN),并将大鼠分为不同组,给予 Adropinin 剂量依赖性治疗。测定血糖水平、体重、组织重量、抗氧化、肾、肝参数和细胞因子。实验研究结束时进行肾脏组织病理学检查。
Adropinin 显著(P<0.001)提高了血浆胰岛素水平,降低了血糖水平。Adropinin 显著增加了体重,减少了肾脏重量和肾脏肥大。Adropinin 显著(P<0.001)减少了尿流量、微量白蛋白、总蛋白、血尿素氮(BUN)、尿酸,并增加了肌酐、肌酐清除率。Adropinin 显著(P<0.001)降低了血清、肾脏中的吲哚硫酸水平,并减少了尿液中的吲哚硫酸水平。Adropinin 显著(P<0.001)降低了总胆固醇、甘油三酯、低密度脂蛋白(LDL)、极低密度脂蛋白(VLDL),并增加了高密度脂蛋白(HDL)水平。Adropinin 显著(P<0.001)增加了谷胱甘肽(GSH)、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)等抗氧化酶的水平,并降低了丙二醛(MDA)、8-羟基-2'-脱氧鸟苷(8-OHdG)的水平。Adropinin 显著(P<0.001)降低了白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、转化生长因子β(TGF-β)的水平,增加了白细胞介素-10(IL-10)的水平。Adropinin 治疗显示出改善肾脏组织病理学的作用。
我们可以说,Adropinin 通过炎症和抗氧化途径对 STZ 诱导的糖尿病肾病大鼠表现出肾保护作用。