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靶向肺血管内皮功能障碍治疗肺动脉高压的研究进展OACSTPCD

Research progress of targeted pulmonary vascular endothelial dysfunction in treatment of pulmonary hypertension

中文摘要英文摘要

肺动脉高压(pulmonary hypertension,PH)是一种进行性、致命性疾病,肺动脉内皮细胞(pulmonary arterial endothe-lial cells,PAECs)功能障碍是其重要的致病因素之一.PAECs是单层扁平上皮细胞,在维持肺血管稳态调控中发挥重要作用.研究发现,在PH发生的早期,PAECs出现损伤及凋亡的现象,而在PH发展的晚期,PAECs则呈现抗凋亡的特征.缺氧、炎症因子诱导的PAECs向间充质细胞的转化,也参与了PH的发病过程.PAECs的癌样代谢和线粒体功能障碍、骨形态发生蛋白受体2突变、表观遗传学改变和炎症,是导致PH患者肺血管内皮功能障碍的主要发病机制.新的靶向PAECs功能障碍的治疗措施,有望在未来治疗PH中发挥重要作用.

Pulmonary hypertension(PH)is a progressive and fatal disease.The dysfunction of pulmonary artery endothelial cells(PAECs)is one of its important pathogenic factors.PAECs are monolayer flat epithelial cells,which play an impor-tant role in maintaining pulmonary vascular homeostasis.Studies have found that PAECs show damage and apoptosis at the early stage of PH development,while PAECs show anti-apoptotic characteristics at the late stage of PH development.The transi-tion of PAECs into mesenchymal cells induced by hypoxic and inflammatory factors is also involved in the pathogenesis of PH.Carcinoid metabolism and mitochondrial dysfunction,bone mor-phogenic type 2 receptor mutation,epigenetic changes and in-flammation of PAECs are the main pathogenesis of pulmonary vascular endothelial dysfunction in PH patients.New therapeutic measures targeting PAECs dysfunction are expected to play an important role in the treatment of PH in the future.

李娜;李占强;芦殿香

青海大学高原医学研究中心||高原医学教育部重点实验室、青海省高原医学应用基础重点实验室(青海-犹他高原医学联合重点实验室)||青海大学附属医院,青海西宁 810000青海大学高原医学研究中心||高原医学教育部重点实验室、青海省高原医学应用基础重点实验室(青海-犹他高原医学联合重点实验室)青海大学高原医学研究中心||高原医学教育部重点实验室、青海省高原医学应用基础重点实验室(青海-犹他高原医学联合重点实验室)||成都大学附属医院,四川成都 610086

肺动脉高压内皮细胞功能障碍表型发病机制治疗

pulmonary hypertensionendothelial cellsdys-functionphenotype pathogenesistreatment

《中国药理学通报》 2024 (001)

藏药三味檀香散保护低氧性肺动脉高压大鼠右心室结构和功能的物质基础及作用机制

1-5 / 5

国家自然科学基金资助项目(No 82374148,82060786,81860768);青海省科技厅自然科学基金面上资助项目(No 2021-ZJ-907);青海省昆仑英才·高端创新创业领军人才项目;青海省昆仑英才·高端创新创业拔尖人才项目

10.12360/CPB202206011

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