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作 者:Jiachi Yu Jia Huang Tian Xia Mianyang Li Ruibing Li
机构地区:[1]Department of Laboratory Medicine,The First Medical Center of Chinese PLA General Hospital,Beijing,China [2]Medical School of Chinese PLA,Beijing,China [3]Beijing Traditional Chinese Medicine Hospital,Capital Medical University,Beijing,China
出 处:《Portal Hypertension & Cirrhosis》2024年第4期217-233,共17页门静脉高压与肝硬化(英文)
基 金:Chinese PLA General Hospital Innovation Support Program,Grant/Award Number:22QNCZ058;National Natural Science Foundation of China,Grant/Award Number:82000537。
摘 要:Alcohol-associated liver disease(ALD)and nonalcoholic fatty liver disease(NAFLD)are the two predominant forms of chronic liver disease worldwide.Regardless of alcohol consumption,patients with NAFLD and ALD exhibit disturbances in lipid metabolism,progressing from simple steatosis to steatohepatitis,fibrosis,and ultimately cirrhosis.The precise mechanisms underlying the pathogenesis of NAFLD and ALD remain unclear.However,numerous studies have highlighted mitochondrial dysfunction as a hallmark of both diseases.Beyond their canonical metabolic function,mitochondria could influence hepatocytes through oxidative stress,intracellular signaling transduction,inflammation,and cell death,all of which are regulated by the mitochondrial quality control(MQC)system.Abnormalities in MQC,including defective mitophagy,erroneous mitochondrial dynamics,and delayed biogenesis,comprise mitochondrial morphological structure,function,and lifespan,resulting in hepatocyte damage.This review explores the involvement of MQC in the pathogenesis of NAFLD and ALD and identifies promising therapeutic targets aimed at enhancing MQC,potentially alleviating metabolic liver disease.
关 键 词:alcohol-associated liver disease mitochondrial dynamics mitochondrial quality control MITOPHAGY nonalcoholic fatty liver disease
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