神经退行性变
褪黑素
微生物群
微粒
肠-脑轴
肠道微生物群
神经科学
生物
医学
生物信息学
病理
生态学
疾病
作者
Samir Ranjan Panda,Vishal Balu Chaudhari,Sahabuddin Ahmed,Mohit Kwatra,Aishwarya Jala,Srikanth Ponneganti,Sharad Pawar,Roshan M. Borkar,Pawan Sharma,V.G.M. Naidu
标识
DOI:10.1016/j.etap.2023.104183
摘要
Exposure to ambient particulate matter (PM2.5) has been shown to disturb the gut microbiome homeostasis and cause initiation of neuroinflammation and neurodegeneration via gut-brain bi-directional axis. Polyaromatic hydrocarbons (PAHs), which are carcinogenic and mutagenic, are important organic constituents of PM2.5 that could be involved in the microbiome-gut-brain axis-mediated neurodegeneration. Melatonin (ML) has been shown to modulate the microbiome and curb inflammation in the gut and brain. However, no studies have been reported for its effect on PM2.5-induced neuroinflammation. In the current study, it was observed that treatment with ML at 100 µM significantly inhibits microglial activation (HMC-3 cells) and colonic inflammation (CCD-841 cells) by the conditioned media from PM2.5 exposed BEAS2B cells. Further, melatonin treatment at a dose of 50 mg/kg to C57BL/6 mice exposed to PM2.5 (at a dose of 60 µg/animal) for 90 days significantly alleviated the neuroinflammation and neurodegeneration caused by PAHs in PM2.5 by modulating olfactory-brain and microbiome-gut-brain axis.
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