Early-life noise exposure causes cognitive impairment in a sex-dependent manner by disrupting homeostasis of the microbiota-gut-brain axis.

Xiaofang Li, Bo Fu, Chunli Zhao, Junjie Hu,Xinyao Zhang, Yiming Fu,Xiaojun She, Cui Gu, Mengzhu Cheng, Fenghan Wang, Xiaoqiong Song, Jie Dai,Jiayi Yin, Yu Fu,Pengfang Zheng,Fangshan Wu,Yingwen Zhu,Kefeng Ma,Xiujie Gao, Miao Wang,Qiang Zeng,Bo Cui

Brain, behavior, and immunity(2023)

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摘要
Epidemiological investigations show that noise exposure in early life is associated with health and cognitive impairment. The gut microbiome established in early life plays a crucial role in modulating developmental processes that subsequently affect brain function and behavior. Here, we examined the impact of early-life exposure to noise on cognitive function in adolescent rats by analyzing the gut microbiome and metabolome to elucidate the underlying mechanisms. Chronic noise exposure during early life led to cognitive deficits, hippocampal injury, and neuroinflammation. Early-life noise exposure showed significant difference on the composition and function of the gut microbiome throughout adolescence, subsequently causing axis-series changes in fecal short-chain fatty acid (SCFA) metabolism and serum metabolome profiles, as well as dysregulation of endothelial tight junction proteins, in both intestine and brain. We also observed sex-dependent effects of microbiota depletion on SCFA-related beneficial bacteria in adolescence. Experiments on microbiota transplantation and SCFA supplementation further confirmed the role of intestinal bacteria and related SCFAs in early-life noise-exposure-induced impairments in cognition, epithelial integrity, and neuroinflammation. Overall, these results highlight the homeostatic imbalance of microbiota-gut-brain axis as an important physiological response toward environmental noise during early life and reveals subtle differences in molecular signaling processes between male and female rats.
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关键词
Noise exposure,Early-life,Gut microbiota,Short-chain fatty acid,Inflammatory response,Cognitive function,Sex-dependent
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