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线粒体作为肠道微生物群与动脉粥样硬化之间联系的新型介质,而草药可改善这种联系:综述。

Mitochondria as novel mediators linking gut microbiota to atherosclerosis that is ameliorated by herbal medicine: A review.

作者信息

Li Yujuan, Yang Shengjie, Jin Xiao, Li Dan, Lu Jing, Wang Xinyue, Wu Min

机构信息

Guang'an Men Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Pharmacol. 2023 Jan 17;14:1082817. doi: 10.3389/fphar.2023.1082817. eCollection 2023.

Abstract

Atherosclerosis (AS) is the main cause of cardiovascular disease (CVD) and is characterized by endothelial damage, lipid deposition, and chronic inflammation. Gut microbiota plays an important role in the occurrence and development of AS by regulating host metabolism and immunity. As human mitochondria evolved from primordial bacteria have homologous characteristics, they are attacked by microbial pathogens as target organelles, thus contributing to energy metabolism disorders, oxidative stress, and apoptosis. Therefore, mitochondria may be a key mediator of intestinal microbiota disorders and AS aggravation. Microbial metabolites, such as short-chain fatty acids, trimethylamine, hydrogen sulfide, and bile acids, also affect mitochondrial function, including mtDNA mutation, oxidative stress, and mitophagy, promoting low-grade inflammation. This further damages cellular homeostasis and the balance of innate immunity, aggravating AS. Herbal medicines and their monomers can effectively ameliorate the intestinal flora and their metabolites, improve mitochondrial function, and inhibit atherosclerotic plaques. This review focuses on the interaction between gut microbiota and mitochondria in AS and explores a therapeutic strategy for restoring mitochondrial function and intestinal microbiota disorders using herbal medicines, aiming to provide new insights for the prevention and treatment of AS.

摘要

动脉粥样硬化(AS)是心血管疾病(CVD)的主要病因,其特征为内皮损伤、脂质沉积和慢性炎症。肠道微生物群通过调节宿主代谢和免疫在AS的发生发展中起重要作用。由于人类线粒体由原始细菌进化而来,具有同源特征,它们作为靶细胞器受到微生物病原体的攻击,从而导致能量代谢紊乱、氧化应激和细胞凋亡。因此,线粒体可能是肠道微生物群紊乱和AS加重的关键介质。微生物代谢产物,如短链脂肪酸、三甲胺、硫化氢和胆汁酸,也会影响线粒体功能,包括线粒体DNA突变、氧化应激和线粒体自噬,促进低度炎症。这进一步破坏细胞稳态和先天免疫平衡,加重AS。草药及其单体可有效改善肠道菌群及其代谢产物,改善线粒体功能,抑制动脉粥样硬化斑块形成。本综述重点关注AS中肠道微生物群与线粒体之间的相互作用,并探索利用草药恢复线粒体功能和肠道微生物群紊乱的治疗策略,旨在为AS的预防和治疗提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d0c/9886688/06c72a94eee3/fphar-14-1082817-g001.jpg

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