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Novel mechanistic insights into treadmill exercise based rescue of social defeat-induced anxiety-like behavior and memory impairment in rats

机译:基于跑步机锻炼的社会机制诱发的焦虑样行为和记忆障碍的抢救的新型机制

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摘要

Social defeat (SD) induced stress causes physiological and behavioral deficits in rodents, including depression and anxiety-like behaviors, as well as memory impairment. Anxiolytic and mood elevating effects of physical exercise are also known. However, rescue effect of physical exercise in social defeat-induced anxiety, depression or memory impairment has not been addressed. Role of epigenetic mechanisms that potentially contribute to these rescue or protective effects are also not known. Present study investigated the effect of moderate treadmill exercise on anxiety-like behavior and memory function in rats subjected to SD using a modified version of the resident-intruder model for social stress (defeat). Changes in histone acetylation and histone-modifying enzymes were examined in hippocampus, amygdala and frontal cortex which are considered critical for anxiety, depression and cognition. Sprague Dawley rats were randomly assigned in four groups; control, exercised, social defeat, social defeat and exercise. At the end of the SD or control exposure lasting 30 min daily for 7 days, one group of SD rats was subjected to treadmill exercise for 2 weeks, whereas the other SD group was handled without exercise. Anxiety-like behavior tests and radial arm water maze test suggested that moderate treadmill exercise rescued social defeat induced anxiety-like behavior and memory impairment. Moreover, exercise normalized SD-induced increase in oxidative stress, most likely by adjusting antioxidant response. Our data suggests involvement of epigenetic mechanisms including histone acetylation of H3 and modulation of methyl-CpG-binding in the hippocampus that might contribute to the rescue effects of exercise in SD-induced behavioral deficits in rats.
机译:社会挫败(SD)诱发的压力导致啮齿动物的生理和行为缺陷,包括抑郁和焦虑样行为,以及记忆力减退。体育锻炼的抗焦虑和提高情绪的作用也是已知的。然而,尚未解决体育锻炼对社交失败引起的焦虑,抑郁或记忆障碍的挽救作用。还不知道可能有助于这些拯救或保护作用的表观遗传机制的作用。本研究使用改良版的居民-入侵者模型应对社会压力(失败),研究了适度的跑步机运动对SD大鼠的焦虑样行为和记忆功能的影响。在海马,杏仁核和额叶皮层检查了组蛋白乙酰化和组蛋白修饰酶的变化,这些变化被认为对焦虑,抑郁和认知至关重要。将Sprague Dawley大鼠随机分为四组。控制,锻炼,社交失败,社交失败和锻炼。在SD或对照暴露持续30天每天7天结束时,一组SD大鼠接受跑步机运动2周,而另一组SD大鼠则不运动。焦虑样行为测试和radial水迷宫测试表明,适度的跑步机锻炼可以挽救社交失败引起的焦虑样行为和记忆障碍。此外,运动可能是通过调节抗氧化剂的反应使SD引起的氧化应激标准化增高。我们的数据表明表观遗传机制的参与,包括H3的组蛋白乙酰化和海马中甲基CpG结合的调节,这可能有助于运动对SD诱发的大鼠行为缺陷的挽救作用。

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