Department of Gastroenterology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, Jiangsu 223300, P. R. China.
Department of Endocrinology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, Jiangsu 223300, P. R. China.
Food Funct. 2017 Jan 25;8(1):299-306. doi: 10.1039/c6fo01601d.
The present study was designed to investigate the protective effect of betulinic acid (BA) on streptozotocin (STZ)-induced diabetic rats. The rats were intraperitoneally injected with STZ (35 mg kg). 7 days later, the animals were intragastrically administered with metformin (MET, 150 mg kg), BA (20 mg kg) or BA (40 mg kg) once daily for consecutive 30 days. The blood glucose, the contents of insulin, interleukin-6 (IL-6), interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) in serum were examined. The levels of IL-6, IL-1β, TNF-α, superoxide dismutase (SOD), catalase (CAT) and malondialdehyde (MDA) in kidney tissues were measured. Moreover, the histopathological alteration and the protein expressions of the signaling pathway were detected by hematoxylin and eosin (H&E) staining and western blotting, respectively. BA significantly decreased the levels of serum insulin, IL-6, IL-1β, TNF-α and blood glucose. In addition, BA increased the activities of SOD, CAT and reduced the contents of MDA, IL-6, IL-1β, and TNF-α in kidney tissues. BA also ameliorated the histopathological condition. Furthermore, BA attenuated the phosphorylations of p-adenosine 5'-monophosphate-activated protein kinase (AMPK), nuclear factor kappaB (NF-κB), and an inhibitor of NF-κB (IκBα) and the expressions of NF-E2-related factor 2 (Nrf2) and heme oxygenase (HO)-1. These findings demonstrated that BA exhibited a protective effect on diabetic nephropathy in STZ-induced rats possibly through the AMPK/NF-κB/Nrf2 pathway.
本研究旨在探讨白桦酸(BA)对链脲佐菌素(STZ)诱导的糖尿病大鼠的保护作用。大鼠腹腔注射 STZ(35mg/kg)。7 天后,动物每天经胃内给予二甲双胍(MET,150mg/kg)、BA(20mg/kg)或 BA(40mg/kg)连续 30 天。检测血清中血糖、胰岛素含量、白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)的含量。测定肾组织中 IL-6、IL-1β、TNF-α、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和丙二醛(MDA)的水平。此外,通过苏木精和伊红(H&E)染色和蛋白质印迹法分别检测信号通路的组织病理学改变和蛋白表达。BA 显著降低了血清胰岛素、IL-6、IL-1β、TNF-α和血糖水平。此外,BA 增加了 SOD、CAT 的活性,降低了肾组织中 MDA、IL-6、IL-1β和 TNF-α的含量。BA 还改善了组织病理学状况。此外,BA 减弱了磷酸化腺苷 5'-单磷酸激活蛋白激酶(AMPK)、核因子 kappaB(NF-κB)和 NF-κB 抑制剂(IκBα)以及核因子红细胞 2 相关因子 2(Nrf2)和血红素加氧酶(HO)-1 的表达。这些结果表明,BA 通过 AMPK/NF-κB/Nrf2 通路对 STZ 诱导的糖尿病大鼠的糖尿病肾病表现出保护作用。