Institute of Basic Medical Sciences, National Cheng Kung University Medical College, Tainan, Taiwan.
J Physiol. 2013 Feb 15;591(4):985-1000. doi: 10.1113/jphysiol.2012.241125. Epub 2012 Nov 26.
Closed-head injury (CHI) usually involves both physical damage of neurons and neuroinflammation. Although exercise promotes neuronal repair and suppresses neuroinflammation, CHI patients currently often remain resting during the post-traumatic period. This study aimed to investigate whether and how postinjury exercise benefited the brain structure and function in mice after CHI. Closed-head injury immediately caused an elevated neurological severity score, with rapid loss of object recognition memory, followed by progressive location-dependent brain damage (neuronal loss and activation of microglia in the cortex and hippocampus). An early exercise protocol at moderate intensity (starting 2 days postimpact and lasting for 7 or 14 days) effectively restored the object recognition memory and prevented the progressive neuronal loss and activation of microglia. However, if the exercise started 9 days postimpact, it was unable to recover recognition memory deficits. In parallel, early exercise intervention drastically promoted neurite regeneration, while late exercise intervention was much less effective. We also tested the possible involvement of brain-derived neurotrophic factor (BDNF) and mitogen-activated protein kinase phosphatase-1 (MKP-1) in the exercise-induced beneficial effects. Exercise gradually restored the impact-abolished hippocampal expression of BDNF and MPK-1, while oral administration of triptolide (a synthesis inhibitor of MKP-1 and an antagonist of nuclear factor-B) before each bout of exercise blocked the restorative effects of exercise on MKP-1 and recognition memory, as well as the exercise-induced retardation of neuronal loss. Although triptolide treatment alone inhibited activation of microglia and maintained neuronal numbers, it did not recover the injury-hampered recognition memory. Overall, moderate exercise shortly after CHI reversed the deficits in recognition memory and prevented the progression of brain injury.
闭合性颅脑损伤(CHI)通常涉及神经元的物理损伤和神经炎症。尽管运动促进神经元修复并抑制神经炎症,但 CHI 患者在创伤后通常仍处于休息状态。本研究旨在探讨创伤后运动是否以及如何有益于 CHI 后小鼠的大脑结构和功能。闭合性颅脑损伤立即导致神经严重程度评分升高,伴有物体识别记忆迅速丧失,随后出现位置依赖的进行性脑损伤(皮质和海马区神经元丢失和小胶质细胞激活)。中等强度的早期运动方案(在撞击后 2 天开始,持续 7 或 14 天)可有效恢复物体识别记忆并防止进行性神经元丢失和小胶质细胞激活。然而,如果运动在撞击后 9 天开始,则无法恢复识别记忆缺陷。平行地,早期运动干预极大地促进了神经突再生,而晚期运动干预则效果较差。我们还测试了脑源性神经营养因子(BDNF)和丝裂原活化蛋白激酶磷酸酶-1(MKP-1)在运动诱导的有益作用中的可能参与。运动逐渐恢复了海马区 BDNF 和 MPK-1 的表达,而在每次运动前口服雷公藤内酯(MKP-1 的合成抑制剂和核因子-B 的拮抗剂)可阻断运动对 MKP-1 和识别记忆的恢复作用,以及运动对神经元丢失的延缓作用。尽管雷公藤内酯单独处理可抑制小胶质细胞激活并维持神经元数量,但无法恢复损伤造成的识别记忆障碍。总的来说,CHI 后适度运动可逆转识别记忆缺陷并防止脑损伤进展。