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认知衰老可改变生活方式因素结局中的性别差异:神经炎症和小胶质细胞作为关键潜在机制。

Sex differences in the outcomes of modifiable lifestyle factors for cognitive aging: neuroinflammation and microglia as key underlying mechanisms.

作者信息

Coleborn Samantha G, Gilson Zoë M, Guo Yunyong, Tremblay Marie-Ève

机构信息

Institute on Aging and Lifelong Health, University of Victoria, Victoria, BC, Canada.

Department of Psychology, University of Victoria, Victoria, BC, Canada.

出版信息

Front Aging Neurosci. 2025 Jul 22;17:1642043. doi: 10.3389/fnagi.2025.1642043. eCollection 2025.

Abstract

Microglia are the resident immune cells of the brain. Over the past two decades, they have been shown to play critical roles throughout life. Microglia are now considered to be important for brain formation, maturation, activity and plasticity, with outcomes on behavior and other cognitive domains. With this knowledge, microglia represent a promising therapeutic target to promote brain health along an aging trajectory. Emerging evidence also indicates that modifiable lifestyle factors for cognitive aging can influence the brain and behavior by acting on microglia. The mechanisms identified so far involve their roles in synaptic plasticity, axonal myelination, and adult neurogenesis, exerted through the modulation of brain inflammation ('neuroinflammation'), the release of trophic factors, and phagocytosis. In this mini-review, we will cover the outcomes of exercise, diet. and social isolation on microglial functions during aging. Sex differences in the identified outcomes on cognitive aging and the underlying mechanisms will be highlighted. Our goal with this mini-review is to stimulate further research on this important topic.

摘要

小胶质细胞是大脑中的常驻免疫细胞。在过去二十年中,已表明它们在整个生命过程中发挥着关键作用。小胶质细胞现在被认为对大脑的形成、成熟、活动和可塑性很重要,并影响行为和其他认知领域。基于这一认识,小胶质细胞是促进大脑在衰老过程中保持健康的一个有前景的治疗靶点。新出现的证据还表明,可改变的认知衰老生活方式因素可通过作用于小胶质细胞来影响大脑和行为。迄今为止确定的机制包括它们通过调节脑内炎症(“神经炎症”)、释放营养因子和吞噬作用,在突触可塑性、轴突髓鞘形成和成年神经发生中所起的作用。在这篇小型综述中,我们将探讨衰老过程中运动、饮食和社会隔离对小胶质细胞功能的影响。我们将突出已确定的认知衰老结果中的性别差异及其潜在机制。这篇小型综述的目的是激发对这一重要主题的进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d29e/12321788/6cf95a63d8b1/fnagi-17-1642043-g001.jpg

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