Liu Xianchu, Mo Yanzhi, Gong Jingbo, Li Zhuang, Peng Huan, Chen Jiaxue, Wang Qichao, Ke Zhaowen, Xie Jingtao
Department of Applied Psychology, Hunan University of Chinese Medicine, Hunan, People's Republic of China.
Metab Brain Dis. 2016 Apr;31(2):417-23. doi: 10.1007/s11011-015-9779-5. Epub 2015 Dec 19.
Previous research has indicated that Diabetes is a high risk of learning and memory deficits. Puerarin, an isoflavonoid extracted from Kudzu roots, has been reported to possess antioxidant, anti-inflammatory, anti-apoptotic and anti-diabetic properties which are useful in the treatment of various diseases. Recently, Puerarin was found to have the effects on learning and memory performances in humans and animal models. However, up to now, there is no detailed evidence on the effect of Puerarin on diabetes-associated cognitive decline (DACD). In this study, we designed to assess the effects of Puerarin on diabetes-associated cognitive decline (DACD) using a streptozotocin (STZ)-injected rat model and exploring its potential mechanism. Diabetic rats were treated with Puerarin (100 mg/kg per d) for 7 days. The learning and memory function was evaluated by morris water maze test. The acetylcholinesterase (AChE), choline acetylase (ChAT), oxidative indicators [malondialdehyde (MDA) and superoxide dismutase (SOD)] and inflammatory cytokine (TNF-a, IL-1β and IL-6) were measured in hippocampus by using corresponding commercial kits. mRNA and Protein levels of Bcl-2 were analyzed by RT-PCR and Westernblot. The results showed that supplementation of Puerarin improved the learning and memory performances compared with the STZ group by the morris water maze test. In addition, Puerarin supplement significantly prevented AChE and MDA activities, increased ChAT and SOD activities, and alleviated the protein level of TNF-α, IL-1β and IL-6 in the hippocampus compared with the STZ group. Moreover, the pretreatment with Puerarin also significantly increased the Bcl-2 expression. It is concluded that Puerarin possesses neuroprotection to ameliorate cognitive deficits in streptozotocin-induced diabetic rats by anti-inflammatory, antioxidant and antiapototic effects.
先前的研究表明,糖尿病患者存在学习和记忆缺陷的高风险。葛根素是从葛根中提取的一种异黄酮,据报道具有抗氧化、抗炎、抗凋亡和抗糖尿病特性,可用于治疗多种疾病。最近,人们发现葛根素对人类和动物模型的学习和记忆能力有影响。然而,到目前为止,尚无关于葛根素对糖尿病相关认知功能下降(DACD)影响的详细证据。在本研究中,我们旨在使用链脲佐菌素(STZ)注射大鼠模型评估葛根素对糖尿病相关认知功能下降(DACD)的影响,并探索其潜在机制。给糖尿病大鼠用葛根素(每日100mg/kg)治疗7天。通过莫里斯水迷宫试验评估学习和记忆功能。使用相应的商业试剂盒测量海马中的乙酰胆碱酯酶(AChE)、胆碱乙酰化酶(ChAT)、氧化指标[丙二醛(MDA)和超氧化物歧化酶(SOD)]以及炎性细胞因子(TNF-α、IL-1β和IL-6)。通过RT-PCR和蛋白质印迹分析Bcl-2的mRNA和蛋白质水平。结果表明,与STZ组相比,通过莫里斯水迷宫试验,补充葛根素改善了学习和记忆能力。此外,与STZ组相比,补充葛根素显著降低了AChE和MDA活性,增加了ChAT和SOD活性,并减轻了海马中TNF-α、IL-1β和IL-6的蛋白质水平。此外,葛根素预处理还显著增加了Bcl-2表达。得出结论,葛根素具有神经保护作用,可通过抗炎、抗氧化和抗凋亡作用改善链脲佐菌素诱导的糖尿病大鼠的认知缺陷。