Mehta Vineet, Parashar Arun, Udayabanu Malairaman
Department of Biotechnology, Bioinformatics and Pharmacy, Jaypee University of Information Technology, Waknaghat, India.
Physiol Behav. 2017 Mar 15;171:69-78. doi: 10.1016/j.physbeh.2017.01.006. Epub 2017 Jan 7.
It is now evident that chronic stress is associated with anxiety, depression and cognitive dysfunction and very few studies have focused on identifying possible methods to prevent these stress-induced disorders. Previously, we identified abundance of quercetin in Urtica dioica extract, which efficiently attenuated stress related complications. Therefore, current study was designed to investigate the effect of quercetin on chronic unpredicted stress (CUS) induced behavioral dysfunction, oxidative stress and neuroinflammation in the mouse hippocampus. Animals were subjected to unpredicted stress for 21days, during which 30mg/kg quercetin was orally administered to them. Effect of CUS and quercetin treatment on animal behavior was assessed between day 22-26. Afterward, the hippocampus was processed to evaluate neuronal damage, oxidative and inflammatory stress. Results revealed that stressed animals were highly anxious (Elevated Plus Maze and Open Field), showed depressive-like behavior (sucrose preference task), performed poorly in short-term and long-term associative memory task (passive avoidance step-through task) and displayed reduced locomotion (open field). Quercetin alleviated behavioral dysfunction in chronically stressed animals. Compared to CUS, quercetin treatment significantly reduced anxiety, attenuated depression, improved cognitive dysfunction and normalized locomotor activity. Further, CUS elevated the levels of oxidative stress markers (TBARS, nitric oxide), lowered antioxidants (total thiol, catalase), enhanced expression of pro-inflammatory cytokines (IL-6, TNF-α, IL-1β and COX-2) in the hippocampus and damaged hippocampal neurons. Quercetin treatment significantly lowered oxidative and inflammatory stress and prevented neural damage. In conclusion, quercetin can efficiently prevent stress induced neurological complications by rescuing brain from oxidative and inflammatory stress.
现在很明显,慢性应激与焦虑、抑郁和认知功能障碍有关,而很少有研究专注于确定预防这些应激诱导疾病的可能方法。此前,我们在荨麻提取物中发现了大量的槲皮素,其能有效减轻与应激相关的并发症。因此,本研究旨在探讨槲皮素对慢性不可预测应激(CUS)诱导的小鼠海马体行为功能障碍、氧化应激和神经炎症的影响。动物接受21天的不可预测应激,在此期间,给它们口服30mg/kg的槲皮素。在第22 - 26天评估CUS和槲皮素治疗对动物行为的影响。之后,对海马体进行处理以评估神经元损伤、氧化应激和炎症应激。结果显示,应激动物高度焦虑(高架十字迷宫和旷场试验),表现出抑郁样行为(蔗糖偏好试验),在短期和长期联想记忆任务(被动回避穿梭试验)中表现不佳,并且运动能力降低(旷场试验)。槲皮素减轻了慢性应激动物的行为功能障碍。与CUS组相比,槲皮素治疗显著降低了焦虑,减轻了抑郁,改善了认知功能障碍并使运动活动恢复正常。此外,CUS提高了氧化应激标志物(丙二醛、一氧化氮)的水平,降低了抗氧化剂(总巯基、过氧化氢酶),增强了海马体中促炎细胞因子(白细胞介素 - 6、肿瘤坏死因子 - α、白细胞介素 - 1β和环氧化酶 - 2)的表达,并损伤了海马体神经元。槲皮素治疗显著降低了氧化应激和炎症应激,并预防了神经损伤。总之,槲皮素可以通过使大脑免受氧化应激和炎症应激,有效预防应激诱导的神经并发症。