Kim Sang-Hoon, Ko Young Jun, Kim Jee-Youn, Sim Young-Je
Department of Sport & Health Sciences, College of Art & Culture, Sangmyung University, Seoul, Korea.
Major in Sport Service Practice, College of Welfare Convergence, Kangnam University, Youngin, Korea.
Int Neurourol J. 2021 May;25(Suppl 1):S35-43. doi: 10.5213/inj.2142164.082. Epub 2021 May 31.
Exercise is known to reduce proinflammatory cytokines production and apoptosis. We investigated the effect of treadmill running on spatial learning memory in terms of activation of nuclear factor kappa B (NF-κB) and mitogen-activated protein kinase (MAPK) signaling pathway in Alzheimer disease (AD) rats. We also evaluated the effect of treadmill running on proinflammatory cytokine production and apoptosis.
Using the stereotaxic frame, amyloid-β (Aβ) was injected into the lateral ventricle of the brain. The rats belong to treadmill running groups were forced to run on a motorized treadmill for 30 minutes per a day during 4 weeks, starting 3 days after Aβ injection. Morris water maze task was done for the determination of spatial learning memory. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay, immunohistochemistry for cleaved caspase-3, and western blot for NF-κB, inhibitory protein of NF-κB (IκB), MAPK signaling pathway, tumor necrosis factor (TNF)-α, interleukin (IL)-1β were done.
Induction of AD increased proinflammatory cytokine secretion by activating the NF-κB/MAPK signaling pathway. These changes induced apoptosis in the hippocampus and reduced spatial learning memory. In contrast, treadmill running inactivated the NF-κB/MAPK signaling pathway and suppressed proinflammatory cytokine production. These changes inhibited apoptosis and improved spatial learning memory.
Current results showed that treadmill running promoted spatial learning memory through suppressing proinflammatory cytokine production and apoptosis via inactivation of NF-κB/MAPK signaling pathway. Treadmill exercise can be considered an effective intervention for symptom relieve of AD.
已知运动可减少促炎细胞因子的产生和细胞凋亡。我们从阿尔茨海默病(AD)大鼠中核因子κB(NF-κB)和丝裂原活化蛋白激酶(MAPK)信号通路的激活方面,研究了跑步机跑步对空间学习记忆的影响。我们还评估了跑步机跑步对促炎细胞因子产生和细胞凋亡的影响。
使用立体定位框架,将淀粉样β蛋白(Aβ)注入脑侧脑室。在Aβ注射后3天开始,属于跑步机跑步组的大鼠在4周内每天被迫在电动跑步机上跑步30分钟。进行莫里斯水迷宫任务以确定空间学习记忆。进行末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)分析、裂解的半胱天冬酶-3免疫组织化学以及NF-κB、NF-κB抑制蛋白(IκB)、MAPK信号通路、肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β的蛋白质印迹分析。
AD的诱导通过激活NF-κB/MAPK信号通路增加了促炎细胞因子的分泌。这些变化诱导海马体中的细胞凋亡并降低空间学习记忆。相反,跑步机跑步使NF-κB/MAPK信号通路失活并抑制促炎细胞因子的产生。这些变化抑制细胞凋亡并改善空间学习记忆。
目前的结果表明,跑步机跑步通过使NF-κB/MAPK信号通路失活来抑制促炎细胞因子的产生和细胞凋亡,从而促进空间学习记忆。跑步机运动可被认为是缓解AD症状的有效干预措施。