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Dietary emulsifier polysorbate 80 exposure accelerates age-related cognitive decline

肠道菌群 失调 脱氧胆酸 毛螺菌科 认知功能衰退 胆汁酸 生物 肠-脑轴 血脑屏障 内分泌学 免疫学 医学 内科学 中枢神经系统 痴呆 生物化学 疾病 16S核糖体RNA 基因 厚壁菌
作者
Lan Zhang,Zhenyu Yin,Xilei Liu,Ge Jin,Y. Wang,Linlin He,Meimei Li,Xiaoqi Pang,Bo Yan,Zexi Jia,Jiahui Ma,Jingge Wei,Fangyuan Cheng,Li Dai,Lu Wang,Zhaoli Han,Qiang Liu,Fanglian Chen,Hailong Cao,Ping Lei
出处
期刊:Brain Behavior and Immunity [Elsevier BV]
卷期号:119: 171-187 被引量:3
标识
DOI:10.1016/j.bbi.2024.03.052
摘要

Gut microbial homeostasis is crucial for the health of cognition in elderly. Previous study revealed that polysorbate 80 (P80) as a widely used emulsifier in food industries and pharmaceutical formulations could directly alter the human gut microbiota compositions. However, whether long-term exposure to P80 could accelerate age-related cognitive decline via gut-brain axis is still unknown. Accordingly, in this study, we used the senescence accelerated mouse prone 8 (SAMP8) mouse model to investigate the effects of the emulsifier P80 intake (1 % P80 in drinking water for 12 weeks) on gut microbiota and cognitive function. Our results indicated that P80 intake significantly exacerbated cognitive decline in SAMP8 mice, along with increased brain pathological proteins deposition, disruption of the blood–brain barrier and activation of microglia and neurotoxic astrocytes. Besides, P80 intake could also induce gut microbiota dysbiosis, especially the increased abundance of secondary bile acids producing bacteria, such as Ruminococcaceae, Lachnospiraceae, and Clostridium scindens. Moreover, fecal microbiota transplantation from P80 mice into 16-week-old SAMP8 mice could also exacerbated cognitive decline, microglia activation and intestinal barrier impairment. Intriguingly, the alterations of gut microbial composition significantly affected bile acid metabolism profiles after P80 exposure, with markedly elevated levels of deoxycholic acid (DCA) in serum and brain tissue. Mechanically, DCA could activate microglial and promote senescence-associated secretory phenotype production through adenosine triphosphate-binding cassette transporter A1 (ABCA1) importing lysosomal cholesterol. Altogether, the emulsifier P80 accelerated cognitive decline of aging mice by inducing gut dysbiosis, bile acid metabolism alteration, intestinal barrier and blood brain barrier disruption as well as neuroinflammation. This study provides strong evidence that dietary-induced gut microbiota dysbiosis may be a risk factor for age-related cognitive decline.
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