Department of Biology, Golden Meditech Center for NeuroRegeneration Sciences, Hong Kong Baptist University, Hong Kong Special Administrative Region.
Institute of Environmental Science, Shanxi University, Taiyuan, PR China.
Ecotoxicol Environ Saf. 2020 Apr 1;192:110325. doi: 10.1016/j.ecoenv.2020.110325. Epub 2020 Feb 18.
Fine particulate matter (PM) was a risk factor for neurological disorders when emerging studies revealed that PM affected the bacterial community structure of gut in Alzheimer's disease (AD) patients. The purpose of this study was to explore the effects of PM on intestinal and brain injury and on bacterial community structure in the intestine and feces of APP/PS1 transgenic mice exposed to PM for eight weeks with a real-world whole-body inhalation exposure system in Taiyuan, China. The brain and intestinal tissues were collected to evaluate histopathological changes by HE staining. TNF-α and IL-6 levels in intestines, brains, and serums, and Aβ-42 levels in brains were detected. Intestinal and fecal samples were subjected to 16S rRNA gene sequencing. Results showed that PM significantly aggravated the pathological injury in intestines and brains in AD mice with elevated pro-inflammatory cytokine levels. The estimators of Shannon, Simpson, Chao1, and ACE indexes reflected the diversity and richness of the bacterial community. Compared with the FA-WT group, the FA-AD group had lower diversity and richness when the PM-AD group had the highest ones. PCA and NMDS revealed the specific influence of PM on the bacterial community of intestine and feces because that the PM-FA and PM-AD group clumped visibly closer than the other groups in both bacterial communities of intestine and feces. The KEGG pathway analysis predicted the vital functional genes and metabolic pathways in the bacterial community of PM-AD mice. This study indicated the histopathological changes and inflammation in the intestine and brain were seriously caused in PM-AD mice when the α-diversity of the bacterial community in intestine and feces was visibly changed.
细颗粒物(PM)是神经紊乱的一个风险因素,因为新出现的研究表明 PM 会影响阿尔茨海默病(AD)患者肠道中的细菌群落结构。本研究的目的是在中国太原的真实全身体吸入暴露系统中,探索 PM 对 APP/PS1 转基因小鼠肠道和大脑损伤以及肠道和粪便中细菌群落结构的影响,这些小鼠在 8 周内暴露于 PM。收集大脑和肠道组织,通过 HE 染色评估组织病理学变化。检测肠道、大脑和血清中的 TNF-α 和 IL-6 水平以及大脑中的 Aβ-42 水平。对肠道和粪便样本进行 16S rRNA 基因测序。结果表明,PM 显著加重了 AD 小鼠的肠道和大脑病理损伤,同时提高了促炎细胞因子水平。香农、辛普森、Chao1 和 ACE 指数的估计值反映了细菌群落的多样性和丰富度。与 FA-WT 组相比,FA-AD 组的多样性和丰富度较低,而 PM-AD 组的多样性和丰富度最高。PCA 和 NMDS 显示了 PM 对肠道和粪便细菌群落的具体影响,因为在肠道和粪便细菌群落中,PM-FA 和 PM-AD 组明显比其他组更紧密地聚集在一起。KEGG 途径分析预测了 PM-AD 小鼠肠道细菌群落中的重要功能基因和代谢途径。本研究表明,当肠道和粪便中细菌群落的α多样性明显改变时,PM-AD 小鼠的肠道和大脑的组织病理学变化和炎症明显加重。