College of Food and Biotechnology, Shaanxi University of Science and Technology, Xi'an, 710021, China.
School of Chemistry and Chemical Engineering, Xi'an University of Science and Technology, Xi'an, 710054, China.
Environ Toxicol Pharmacol. 2017 Sep;54:80-92. doi: 10.1016/j.etap.2017.06.021. Epub 2017 Jun 28.
Diabetic nephropathy (DN) is the most severe complication of diabetes and multiple factors are involved in the pathogenesis of DN. Among them, cadmium (Cd) acts as a risk factor inducing the occurrence of DN. The present study focused on investigating the protective role of caffeic acid phenethyl ester (CAPE), an active component of propolis from honeybee hives, against Cd-induced DN in mice based on ultra performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS)and pattern recognition. Serum and urine biochemical indexes were detected and histopathological observation has been done to evaluate the damage of Cd on animals. Moreover, the global serum profiles of different groups were distinguished by UPLC-Q-TOF-MS and principal component analysis (PCA) were applied for group differentiation and marker selection. Moreover, the influence of Cd on the oxidative status in DN mice were also evaluated by assessing the parameters of oxidative stress, proinflammatory cytokines and antioxidant competence. As shown in the scores plots, the distinct clustering among controls, DN and CAPE groups were observed, significant changes in serum levels of LysoPC(18:1(11Z)), 2,3-dinor-8-iso-PGF2a, PS(18:1(9Z)/18:1(9Z)), DG(17:0/22:4 (7Z,10Z, 13Z, 16Z)/0:0) and Arachidonic acid(AA) were noted and identified as potential biomarkers, the effect of CAPE reverted them back to near normalcy. Further, It was observed a significant improvement in lipid peroxides (LPO) and protein carbonyls (PCO) levels in Cd-induced DN kidneys along with a significant decline in superoxide dismutase (SOD), catalase (CAT), and reduced glutathione (GSH) levels, however, CAPE relieved these changes. In conclusion, the study suggested that the pathogenesis of DN caused by Cd probably owes to the perturbations of lipid metabolism and AA metabolism; CAPE seems to be effective agent and may be related to its potent antioxidant, anti-inflammatory properties and action as an Nrf2 activator.
糖尿病肾病(DN)是糖尿病最严重的并发症,其发病机制涉及多种因素。其中,镉(Cd)作为诱导 DN 发生的危险因素之一。本研究基于超高效液相色谱-四极杆飞行时间质谱联用(UPLC-Q-TOF-MS)和模式识别技术,聚焦于研究咖啡酸苯乙酯(CAPE),一种来自蜜蜂蜂巢的蜂胶活性成分,对 Cd 诱导的小鼠 DN 的保护作用。检测血清和尿液生化指标,并进行组织病理学观察,以评估 Cd 对动物的损伤。此外,通过 UPLC-Q-TOF-MS 对不同组别的血清进行全局分析,并应用主成分分析(PCA)进行组间区分和标志物选择。此外,还通过评估氧化应激、促炎细胞因子和抗氧化能力的参数来评估 Cd 对 DN 小鼠氧化状态的影响。结果表明,在得分图中,观察到对照组、DN 组和 CAPE 组之间的明显聚类,血清中 LysoPC(18:1(11Z))、2,3-二去-8-异-PGF2a、PS(18:1(9Z)/18:1(9Z))、DG(17:0/22:4 (7Z,10Z, 13Z, 16Z)/0:0)和花生四烯酸(AA)的水平发生显著变化,并将其鉴定为潜在的生物标志物,CAPE 可使这些标志物水平恢复正常。此外,还观察到 Cd 诱导的 DN 肾脏中的脂质过氧化物(LPO)和蛋白羰基(PCO)水平显著降低,而过氧化物歧化酶(SOD)、过氧化氢酶(CAT)和还原型谷胱甘肽(GSH)水平显著升高,而 CAPE 缓解了这些变化。综上所述,本研究表明,Cd 引起的 DN 发病机制可能归因于脂质代谢和 AA 代谢的紊乱;CAPE 可能是一种有效的药物,其作用可能与其强大的抗氧化、抗炎特性以及作为 Nrf2 激活剂有关。