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通过肿瘤坏死因子受体的肿瘤坏死因子信号传导介导运动对认知样行为的影响。

TNF signalling via the TNF receptors mediates the effects of exercise on cognition-like behaviours.

作者信息

Morgan Julie A, Singhal Gaurav, Corrigan Frances, Jaehne Emily J, Jawahar Magdalene C, Baune Bernhard T

机构信息

The University of Adelaide, School of Medicine, Discipline of Psychiatry, Adelaide, Australia.

The University of Adelaide, School of Medicine, Discipline of Medical Sciences, Adelaide, Australia.

出版信息

Behav Brain Res. 2018 Nov 1;353:74-82. doi: 10.1016/j.bbr.2018.06.036. Epub 2018 Jun 30.

Abstract

BACKGROUND

Altered TNF levels are associated with cognitive impairment in depression, schizophrenia, bipolar disorder, and Alzheimer's disease (AD). Exercise improves cognition-like behaviours, reduces the expression of tumour necrosis factor alpha (TNF), and increases expression of the soluble TNF receptors soluble TNFR1 (sTNFR1) and sTNFR2. We suggest TNF and its receptors are involved in cognitive function and dysfunction, and investigate whether exercise mediates its effects on cognitive function via TNF and its receptors.

METHODS

We utilised C57BL/6, TNF, TNFR1, and TNFR2 mice to compare exercise to non-exercise control groups to investigate whether exercise exerts its effects on various types of cognition-like behaviours via TNF and its receptors.

RESULTS

Recognition memory improved with exercise in WT mice, was impaired in TNFR1 exercise mice, showed non-significant impairment with exercise in TNF mice, and no changes in TNFR2 mice. In spatial learning there were exercise related improvements in WT mice, non-significant but meaningful impairments evident in TNFR1 exercise mice, modest improvement in TNF exercise mice, and potentially meaningful non-significant improvements in TNFR2 exercise mice. Moreover, WT and TNFR2 mice displayed noteworthy non-significant improvements in spatial memory, whereas TNFR1 exercise mice demonstrated non-significant spatial memory impairment. Exercise did not alter cognitive flexibility in any strain.

DISCUSSION

TNF receptor signalling via the TNFR1 and TNFR2 appears to mediate the effects of exercise on cognitive-like behaviours. The potential for exercise to regulate human TNF and TNF signalling and cognitive dysfunction needs investigation under inflammatory conditions including depression and neuropsychiatric disorders.

摘要

背景

肿瘤坏死因子(TNF)水平的改变与抑郁症、精神分裂症、双相情感障碍和阿尔茨海默病(AD)中的认知障碍有关。运动可改善认知样行为,降低肿瘤坏死因子α(TNF)的表达,并增加可溶性TNF受体可溶性TNFR1(sTNFR1)和sTNFR2的表达。我们认为TNF及其受体参与认知功能和功能障碍,并研究运动是否通过TNF及其受体介导其对认知功能的影响。

方法

我们利用C57BL/6、TNF、TNFR1和TNFR2小鼠,将运动组与非运动对照组进行比较,以研究运动是否通过TNF及其受体对各种类型的认知样行为产生影响。

结果

野生型(WT)小鼠运动后识别记忆得到改善,TNFR1运动小鼠的识别记忆受损,TNF小鼠运动后识别记忆有不显著的损伤,而TNFR2小鼠无变化。在空间学习方面,WT小鼠运动后有改善,TNFR1运动小鼠有不显著但有意义的损伤,TNF运动小鼠有适度改善,TNFR2运动小鼠有潜在有意义的不显著改善。此外,WT和TNFR2小鼠在空间记忆方面有值得注意的不显著改善,而TNFR1运动小鼠表现出不显著的空间记忆损伤。运动对任何品系的认知灵活性均无影响。

讨论

通过TNFR1和TNFR2的TNF受体信号似乎介导了运动对认知样行为的影响。在包括抑郁症和神经精神疾病在内的炎症条件下,运动调节人类TNF和TNF信号以及认知功能障碍的潜力需要进一步研究。

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