Oral nano-antioxidants improve sleep by restoring intestinal barrier integrity and preventing systemic inflammation

被引:8
作者
Wu, Zhanfeng [1 ,2 ]
Liu, Lei [1 ,2 ]
Li, Lei [1 ,2 ]
Cao, Xinran [1 ,2 ]
Jia, Wang [1 ,2 ]
Liao, Xiaodan [1 ,2 ]
Zhao, Zhongpu [1 ,2 ]
Qi, Hedong [1 ,2 ]
Fan, Guoqiang [3 ]
Lu, Huiqiang [4 ]
Shu, Chunying [1 ,2 ]
Zhen, Mingming [1 ,2 ]
Wang, Chunru [1 ,2 ]
Bai, Chunli [1 ,2 ]
机构
[1] Chinese Acad Sci, Key Lab Mol Nanostruct & Nanotechnol, CAS Res Educ Ctr Excellence Mol Sci, Beijing Natl Lab Mol Sci,Inst Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Wenzhou Med Univ, Sch Pharm, Wenzhou 325000, Peoples R China
[4] Gannan Normal Univ, Ctr Drug Screening & Res, Sch Geog & Environm Engn, Ganzhou 341000, Peoples R China
关键词
sleep deprivation; fullerene nano-antioxidants; brain-gut axis; reactive oxygen species; inflammation; DISEASE; MICROBIOTA; IMMUNE; RISK;
D O I
10.1093/nsr/nwad309
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sleep deprivation (SD) is a severe public health threat that can cause systemic inflammation and nerve damage. Few effective and side-effect-free drugs are available to address SD. However, the bidirectional communications between the brain and gut provide new strategies for anti-SD therapeutics. Here we explored oraldelivery of fullerene nano-antioxidants (FNAO) in the SD model to improve sleep by regulating abnormal intestinal barrier and systemic inflammation via the brain-gut axis. SD caused excessive reactive oxygen species (ROS) production and hyperactive inflammatory responses in the intestines of zebrafish and mouse models, leading to disturbed sleep patterns and reduced brain nerve activity. Of note, based on the property of the conjugated pi bond of the C60 structure to absorb unpaired electrons, oral FNAO efficiently reduced the excessive ROS in the intestines, maintained redox homeostasis and intestinal barrier integrity, and ameliorated intestinal and systemic inflammation, resulting in superior sleep improvement. Our findings suggest that maintaining intestinal homeostasis may be a promising avenue for SD-related nerve injury therapy.
引用
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页数:13
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