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细胞衰老与特发性肺纤维化药物治疗研究进展

任正肖 张颖颖 车萍 李紫薇 朱庆均

中国药理学通报2024,Vol.40Issue(4):601-605,5.
中国药理学通报2024,Vol.40Issue(4):601-605,5.DOI:10.12360/CPB202206081

细胞衰老与特发性肺纤维化药物治疗研究进展

Research progress in cellular senescence and drug therapy of idiopathic pulmonary fibrosis

任正肖 1张颖颖 1车萍 1李紫薇 1朱庆均1

作者信息

  • 1. 山东中医药大学实验中心,山东中医药大学中医学院微生物教研室,山东中医药大学中医药创新研究院,山东济南 250355
  • 折叠

摘要

Abstract

Idiopathic pulmonary fibrosis(IPF)is a devastating lung disease of unknown etiology characterized by the deposition of extracellular matrix proteins,such as collagen and fibronectin,in the interstitium of the lung,leading to respiratory failure.Our understanding of the pathobiology of IPF remains incomplete;however,it is generally accepted that aging is a major risk factor for the disease.Senescence is a complex process characterized by irreversible cell cycle arrest and secretory senescence-associ-ated phenotype(SASP),leading to the continuous accumulation of senescent cells and the development of inflammation.Cellular senescence is closely related to pulmonary fibrosis disease pro-gression.This review mainly discusses the molecular mechanism of cellular senescence,telomere shortening,mitochondrial dys-function,autophagy deficiency,apoptosis resistance related to cellular cellular in the pathogenesis of IPF and the anti-aging drugs used to treat IPF,so as to provide the theoretical basis and therapeutic methods for the future treatment of IPF.

关键词

特发性肺纤维化/细胞衰老/衰老相关表型/端粒缩短/线粒体功能障碍/自噬不足/细胞凋亡抵抗/治疗

Key words

idiopathic pulmonary fibrosis/cellular senescence/senescence-associated secretory phenotype/telomere shortening/mitochondrial dysfunction/autophagy deficiency/apoptosis re-sistance/treatment

分类

医药卫生

引用本文复制引用

任正肖,张颖颖,车萍,李紫薇,朱庆均..细胞衰老与特发性肺纤维化药物治疗研究进展[J].中国药理学通报,2024,40(4):601-605,5.

基金项目

山东省自然科学基金项目(No ZR2020MH384) (No ZR2020MH384)

山东省重点研发计划(重大科技创新工程)(No 2020CXGC010505) (重大科技创新工程)

中国药理学通报

OA北大核心CSTPCD

1001-1978

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