Long-Term Moderate Exercise Rescues Age-Related Decline in Hippocampal Neuronal Complexity and Memory

被引:43
作者
Tsai, Sheng-Feng [1 ]
Ku, Nai-Wen [2 ]
Wang, Tzu-Feng [2 ]
Yang, Yan-Hsiang [2 ]
Shih, Yao-Hsiang [1 ]
Wu, Shih-Ying [1 ]
Lee, Chu-Wan [1 ,3 ]
Yu, Megan [4 ]
Yang, Ting-Ting [5 ]
Kuo, Yu-Min [1 ,2 ]
机构
[1] Natl Cheng Kung Univ, Inst Basic Med Sci, Coll Med, Tainan, Taiwan
[2] Natl Cheng Kung Univ, Dept Cell Biol & Anat, Coll Med, 1 Univ Rd, Tainan 70101, Taiwan
[3] Ching Kuo Inst Management & Hlth, Dept Nursing, Keelung, Taiwan
[4] Univ Virginia, Dept Chem, Charlottesville, VA USA
[5] I Shou Univ, Sch Chinese Med Postbaccalaureate, 8 Yida Rd, Kaohsiung 82445, Taiwan
关键词
Aging; Memory decline; Treadmill exercise; Spine density; Lactate shuttle; SYNAPTIC POTENTIATION; GLUCOSE-UTILIZATION; ALZHEIMERS-DISEASE; PHYSICAL-ACTIVITY; OXIDATIVE STRESS; GLUTAMATE UPTAKE; IN-VITRO; BRAIN; MICE; RATS;
D O I
10.1159/000488589
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background: Aging impairs hippocampal neuroplasticity and hippocampus-related learning and memory. In contrast, exercise training is known to improve hippocampal neuronal function. However, whether exercise is capable of restoring memory function in old animals is less clear. Objective: Here, we investigated the effects of exercise on the hippocampal neuroplasticity and memory functions during aging. Methods: Young (3 months), middle-aged (9-12 months), and old (18 months) mice underwent moderate-intensity treadmill running training for 6 weeks, and their hippocampus-related learning and memory, and the plasticity of their CA1 neurons was evaluated. Results: The memory performance (Morris water maze and novel object recognition tests), and dendritic complexity (branch and length) and spine density of their hippocampal CA1 neurons decreased as their age increased. The induction and maintenance of high-frequency stimulation-induced long-term potentiation in the CA1 area and the expressions of neuroplasticity-related proteins were not affected by age. Treadmill running increased CA1 neuron long-term potentiation and dendritic complexity in all three age groups, and it restored the learning and memory ability in middle-aged and old mice. Furthermore, treadmill running upregulated the hippocampal expressions of brain-derived neurotrophic factor and monocarboxylate transporter-4 in middle-aged mice, glutamine synthetase in old mice, and full-length TrkB in middle-aged and old mice. Conclusion: The hippocampus-related memory function declines from middle age, but long-term moderate-intensity running effectively increased hippocampal neuroplasticity and memory in mice of different ages, even when the memory impairment had progressed to an advanced stage. Thus, long-term, moderate intensity exercise training might be a way of delaying and treating aging-related memory decline. (C) 2018 S. Karger AG, Basel
引用
收藏
页码:551 / 561
页数:11
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