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药物性肺纤维化的动物模型:分子机制与特征概述。

Animal models of drug-induced pulmonary fibrosis: an overview of molecular mechanisms and characteristics.

机构信息

Department of Pharmacology, School of Basic Medical Sciences, Zhejiang University, Hangzhou, 310058, China.

Department of Clinical Laboratory, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.

出版信息

Cell Biol Toxicol. 2022 Oct;38(5):699-723. doi: 10.1007/s10565-021-09676-z. Epub 2021 Nov 5.

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease characterized by progressive loss of pulmonary function. Drug-induced interstitial lung disease has been reported as a severe adverse effect of some drugs, such as bleomycin, amiodarone, and methotrexate. Based on good characteristics, drug-induced pulmonary fibrosis (PF) animal model has played a key role in our understanding of the molecular mechanisms of PF pathogenesis and recapitulates the specific pathology in patients and helps develop therapeutic strategies. Here, we summarize the mechanisms and characteristics of given fibrotic drug-induced animal models for PFs. Together with the key publications describing these models, this brief but detailed overview would be helpful for the pharmacological research with animal models of PFs. Potential mechanisms underlying drug induced lung toxicity.

摘要

特发性肺纤维化(IPF)是一种进行性间质性肺疾病,其特征是肺功能进行性丧失。药物性间质性肺疾病已被报道为某些药物的严重不良反应,如博来霉素、胺碘酮和甲氨蝶呤。基于良好的特性,药物性肺纤维化(PF)动物模型在我们理解 PF 发病机制的分子机制方面发挥了关键作用,并再现了患者的特定病理学,有助于开发治疗策略。在这里,我们总结了特发性肺纤维化的纤维化药物诱导的动物模型的机制和特征。结合描述这些模型的关键出版物,这一简短但详细的概述将有助于 PF 的动物模型的药理学研究。药物引起的肺毒性的潜在机制。

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