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睡眠剥夺引发小胶质细胞线粒体DNA释放以诱导神经炎症:羟基酪醇丁酸酯的预防作用

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

作者信息

Hu Yachong, Wang Yongyao, Wang Yifang, Zhang Yuxia, Wang Zhen, Xu Xiaohong, Zhang Tinghua, Zhang Tiantian, Zhang Shuangxi, Hu Ranrui, Shi Le, Wang Xudong, Li Jin, Shen Hui, Liu Jiankang, Noda Mami, Peng Yunhua, Long Jiangang

机构信息

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.

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

出版信息

Antioxidants (Basel). 2024 Jul 12;13(7):833. doi: 10.3390/antiox13070833.

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.

摘要

睡眠剥夺(SD)会引发线粒体功能障碍和神经炎症,导致认知障碍和精神问题。然而,涉及线粒体功能障碍和神经炎症的机制仍不清楚。在此,我们报告SD大鼠表现出多种行为障碍、脑氧化应激以及强烈的脑线粒体DNA(mtDNA)氧化。特别地,SD激活了小胶质细胞以及小胶质细胞mtDNA向胞质溶胶的外流,并引发了脑促炎细胞因子。我们观察到,随着mtDNA氧化的抑制,mtDNA外流和促炎细胞因子显著减少。用一种新型线粒体营养物羟基酪醇丁酸酯(HTHB)治疗后,SD诱导的行为障碍得到显著改善,同时大鼠脑和N9小胶质细胞系中的mtDNA氧化、mtDNA释放和NF-κB激活均得到显著缓解。总之,这些结果表明,SD诱导的小胶质细胞mtDNA氧化及其产生的释放介导了神经炎症,而HTHB可防止mtDNA氧化和外流,为SD诱导的精神问题提供了一种潜在的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1051/11273532/882e516f73e5/antioxidants-13-00833-g001.jpg

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