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

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

Antioxidants (Basel)

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.

Published: July 2024

AI Article Synopsis

  • Sleep deprivation can cause problems in the brain like poor thinking and mood issues by messing with tiny energy factories called mitochondria and causing inflammation.
  • In tests with rats that hadn't slept, researchers found that their brains got stressed and damaged, leading to increased inflammation and more harmful substances called cytokines.
  • A new treatment using a special nutrient called hydroxytyrosol butyrate (HTHB) helped improve behavior in sleep-deprived rats and reduced the brain damage, suggesting it might help with mental health problems caused by lack of sleep.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11273532PMC
http://dx.doi.org/10.3390/antiox13070833DOI Listing

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