首页|沉默信息调节因子3通过调节线粒体功能障碍减轻特发性肺纤维化的研究进展

沉默信息调节因子3通过调节线粒体功能障碍减轻特发性肺纤维化的研究进展

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Progress in role of silent information regulator 3 in improving idiopathic pulmonary fibrosis by regulating mitochondrial dysfunction
Idiopathic pulmonary fibrosis(IPF)is a chronic progressive interstitial lung disease of unknown etiology,with a rapid disease course,poor prognosis,and the absence of effective therapeutic drugs.Mitochondrial dys-function is one of the crucial causes of inducing IPF.Silent information regulator 3(SIRT3)can restore mitochondrial ho-meostasis by inhibiting mitochondrial oxidative stress,repairing mitochondrial DNA damage,and ameliorating abnormal mitochondrial lipid metabolism.This paper summarizes the role and mechanism of SIRT3 in attenuating mitochondrial dys-function based on delineating the relationship between mitochondrial dysfunction and IPF,aiming to provide references for finding effective treatment methods for IPF.

idiopathic pulmonary fibrosismitochondrial dysfunctionsilent information regulator 3DNA damagelipid metabolism

杨树森、刘禹杉、张仪霖、惠毅、李京涛、闫曙光

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陕西中医药大学基础医学院,陕西 咸阳 712046

陕西中医药大学附属医院,陕西 咸阳 712000

陕西省胃肠病证方药重点研究室,陕西 咸阳 712046

特发性肺纤维化 线粒体功能障碍 沉默信息调节因子3 DNA损伤 脂质代谢

国家自然科学基金资助项目

81703974

2024

中国病理生理杂志
中国病理生理学会

中国病理生理杂志

CSTPCD北大核心
影响因子:1.065
ISSN:1000-4718
年,卷(期):2024.40(2)
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