Sleep Deprivation Triggers Mitochondrial DNA Release in Microglia to Induce Neural Inflammation: Preventative Effect of Hydroxytyrosol Butyrate

Author:

Hu Yachong1,Wang Yongyao1,Wang Yifang1ORCID,Zhang Yuxia1,Wang Zhen1,Xu Xiaohong2,Zhang Tinghua2,Zhang Tiantian1,Zhang Shuangxi1,Hu Ranrui1,Shi Le1,Wang Xudong1,Li Jin3,Shen Hui4,Liu Jiankang15ORCID,Noda Mami16ORCID,Peng Yunhua1ORCID,Long Jiangang1

Affiliation:

1. Center for Mitochondrial Biology and Medicine, The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi’an Jiaotong University, Xi’an 710049, China

2. School of Pharmacy, Chengdu Medical College, Chengdu 610500, China

3. State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China

4. Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Naval Medical University, Shanghai 200433, China

5. School of Health and Life Science, University of Health and Rehabilitation Sciences, Qingdao 266071, China

6. Research and Educational Resource Center for Immunophenotyping, RUDN University, 6 Miklukho-Maklaya St, 117198 Moscow, Russia

Abstract

Sleep deprivation (SD) triggers mitochondrial dysfunction and neural inflammation, leading to cognitive impairment and mental issues. However, the mechanism involving mitochondrial dysfunction and neural inflammation still remains unclear. Here, we report that SD rats exhibited multiple behavioral disorders, brain oxidative stress, and robust brain mitochondrial DNA (mtDNA) oxidation. In particular, SD activated microglia and microglial mtDNA efflux to the cytosol and provoked brain pro-inflammatory cytokines. We observed that the mtDNA efflux and pro-inflammatory cytokines significantly reduced with the suppression of the mtDNA oxidation. With the treatment of a novel mitochondrial nutrient, hydroxytyrosol butyrate (HTHB), the SD-induced behavioral disorders were significantly ameliorated while mtDNA oxidation, mtDNA release, and NF-κB activation were remarkably alleviated in both the rat brain and the N9 microglial cell line. Together, these results indicate that microglial mtDNA oxidation and the resultant release induced by SD mediate neural inflammation and HTHB prevents mtDNA oxidation and efflux, providing a potential treatment for SD-induced mental issues.

Funder

Space Medical Experiment Project of China Manned Space Program

National Natural Science Foundation of China

Natural Science Basic Research Program of Shaanxi

Basic Scientific Research Foundation of Xi’an Jiaotong University

Young Talent Fund of Association for Science and Technology in Xi’an

China Postdoctoral Science Foundation

National Natural Science Foundation of China Integrated Project of Major Research Plan

General Projects

Publisher

MDPI AG

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