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运动因子鸢尾素通过抑制肠-脑轴介导的炎症减轻认知障碍。

Exerkine irisin mitigates cognitive impairment by suppressing gut-brain axis-mediated inflammation.

作者信息

Zhang Hu, Liang Jiling, Huang Jielun, Wang Minghui, Wu Liangwen, Wu Tong, Chen Ning

机构信息

Tianjiu Research and Development Center for Exercise Nutrition and Foods, Hubei Key Laboratory of Exercise Training and Monitoring, College of Sports Medicine, Wuhan Sports University, Wuhan 430079, China.

Tianjiu Research and Development Center for Exercise Nutrition and Foods, Hubei Key Laboratory of Exercise Training and Monitoring, College of Sports Medicine, Wuhan Sports University, Wuhan 430079, China.

出版信息

J Adv Res. 2024 Oct 29. doi: 10.1016/j.jare.2024.10.031.

Abstract

INTRODUCTION

Exercise has been recognized to improve cognitive performance by optimizing gut flora and up-regulating exerkine irisin.

OBJECTIVE

Although exercise-induced irisin is beneficial to cognitive improvement, whether this benefit is achieved by optimizing gut microbiota and metabolites is not fully explored.

METHODS

After aerobic exercise and exogenous irisin interventions for 12 weeks, the 16S rRNA and metabolites in feces of 21-month-old mice were analyzed. Meanwhile, the differential miRNAs and mRNAs in hippocampal tissues were screened by high-throughput sequencing. Relevant mRNAs and proteins were evaluated by RT-PCR, Western blot, and immunofluorescence.

RESULTS

Compared with the young control mice, irisin levels and cognitive capacity of aged mice revealed a significant reduction, while aerobic exercise and intraperitoneal injection of exogenous irisin reversed aging-induced cognitive impairment. Similarly, 147 up-regulated and 173 down-regulated metabolites were detected in aged mice, while 64 and 45 up-regulated and 225 and 187 down-regulated metabolites were detected in aged mice with exercise and irisin interventions, respectively. Moreover, during hippocampal miRNA and mRNA sequencing analysis, 9 differential gut flora and 35 differential genes were identified to be correlated with the inflammatory signaling mediated by the TLR4/MyD88 signal pathway.

CONCLUSION

Aging-induced cognitive impairment is due to insulin resistance induced by TLR4/MyD88 signaling activation in hippocampal tissues mediated by gut microbiota and metabolite changes. Myokine irisin may be an important mediator in optimizing gut microbiota and metabolism for an improved understanding of mitigated aging process upon exercise interventions.

摘要

引言

运动已被认为可通过优化肠道菌群和上调运动因子鸢尾素改善认知功能。

目的

尽管运动诱导产生的鸢尾素有益于认知功能改善,但这种益处是否通过优化肠道微生物群及其代谢产物来实现尚未得到充分探究。

方法

对21月龄小鼠进行12周的有氧运动和外源性鸢尾素干预后,分析其粪便中的16S rRNA和代谢产物。同时,通过高通量测序筛选海马组织中的差异微小RNA(miRNA)和信使核糖核酸(mRNA)。采用逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和免疫荧光法对相关mRNA和蛋白质进行评估。

结果

与年轻对照小鼠相比,老年小鼠的鸢尾素水平和认知能力显著降低,而有氧运动和腹腔注射外源性鸢尾素可逆转衰老引起的认知障碍。同样,在老年小鼠中检测到147种上调和173种下调的代谢产物,而在运动和鸢尾素干预的老年小鼠中分别检测到64种上调和45种上调以及225种下调和187种下调的代谢产物。此外,在海马miRNA和mRNA测序分析中,鉴定出9种差异肠道菌群和35个差异基因与Toll样受体4(TLR4)/髓样分化因子88(MyD88)信号通路介导的炎症信号相关。

结论

衰老引起的认知障碍是由于肠道微生物群和代谢产物变化介导的海马组织中TLR4/MyD88信号激活诱导的胰岛素抵抗所致。肌动蛋白鸢尾素可能是优化肠道微生物群和代谢的重要介质,有助于更好地理解运动干预对减缓衰老过程的作用。

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