Division of Applied Life Science (BK 21), College of Natural Sciences, Gyeongsang National University, Jinju, 660-701, Republic of Korea.
J Neuroimmune Pharmacol. 2019 Jun;14(2):278-294. doi: 10.1007/s11481-018-9824-3. Epub 2018 Nov 27.
Cognitive decline and memory impairment induced by oxidative brain damage are the critical pathological hallmarks of Alzheimer's disease (AD). Based on the potential neuroprotective effects of melatonin, we here explored the possible underlying mechanisms of the protective effect of melatonin against scopolamine-induced oxidative stress-mediated c-Jun N-terminal kinase (JNK) activation, which ultimately results in synaptic dysfunction, neuroinflammation, and neurodegeneration. According to our findings, scopolamine administration resulted in LPO and ROS generation and decreased the protein levels of antioxidant proteins such as Nrf2 and HO-1; however, melatonin co-treatment mitigated the generation of oxidant factors while improving antioxidant protein levels. Similarly, melatonin ameliorated oxidative stress-mediated JNK activation, enhanced Akt/ERK/CREB signaling, promoted cell survival and proliferation, and promoted memory processes. Immunofluorescence and western blot analysis indicated that melatonin reduced activated gliosis via attenuation of Iba-1 and GFAP. We also found that scopolamine promoted neuronal loss by inducing Bax, Pro-Caspase-3, and Caspase-3 and reducing the levels of the antiapoptotic protein Bcl-2. In contrast, melatonin significantly decreased the levels of apoptotic markers and increased neuronal survival. We further found that scopolamine disrupted synaptic integrity and, conversely, that melatonin enhanced synaptic integrity as indicated by Syntaxin, PSD-95, and SNAP-23 expression levels. Furthermore, melatonin ameliorated scopolamine-induced impairments in spatial learning behavior and memory formation. On the whole, our findings revealed that melatonin attenuated scopolamine-induced synaptic dysfunction and memory impairments by ameliorating oxidative brain damage, stress kinase expression, neuroinflammation, and neurodegeneration. Graphical Abstract The proposed schematic diagram showing the neuroprotective effect of melatonin against scopolamine-induced oxidative stress-mediated synaptic dysfunction, memory impairment neuroinflammation and neurodegeneration.
氧化应激诱导的脑损伤引起的认知能力下降和记忆障碍是阿尔茨海默病(AD)的关键病理特征。基于褪黑素的潜在神经保护作用,我们在这里探讨了褪黑素对东莨菪碱诱导的氧化应激介导的 c-Jun N-末端激酶(JNK)激活的保护作用的潜在机制,氧化应激介导的 JNK 激活最终导致突触功能障碍、神经炎症和神经退行性变。根据我们的发现,东莨菪碱给药导致 LPO 和 ROS 的产生,并降低了抗氧化蛋白(如 Nrf2 和 HO-1)的蛋白水平;然而,褪黑素的共同处理减轻了氧化因子的产生,同时提高了抗氧化蛋白水平。同样,褪黑素改善了氧化应激介导的 JNK 激活,增强了 Akt/ERK/CREB 信号通路,促进了细胞存活和增殖,并促进了记忆过程。免疫荧光和 Western blot 分析表明,褪黑素通过减弱 Iba-1 和 GFAP 来减少激活的神经胶质细胞。我们还发现,东莨菪碱通过诱导 Bax、Pro-Caspase-3 和 Caspase-3 并降低抗凋亡蛋白 Bcl-2 的水平来促进神经元丢失。相比之下,褪黑素显著降低了凋亡标志物的水平并增加了神经元的存活。我们进一步发现,东莨菪碱破坏了突触完整性,而褪黑素则增强了突触完整性,这表现在 Syntaxin、PSD-95 和 SNAP-23 的表达水平上。此外,褪黑素改善了东莨菪碱引起的空间学习行为和记忆形成损伤。总的来说,我们的研究结果表明,褪黑素通过改善氧化脑损伤、应激激酶表达、神经炎症和神经退行性变,减轻了东莨菪碱诱导的突触功能障碍和记忆损伤。