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吡非尼酮抗纤维化作用的药理学基础:来自心脏和模型的机制见解。

Pharmacological basis of the antifibrotic effects of pirfenidone: Mechanistic insights from cardiac and models.

作者信息

Sartiani Laura, Bartolucci Gianluca, Pallecchi Marco, Spinelli Valentina, Cerbai Elisabetta

机构信息

Section of Pharmacology, Department of Neurosciences, Psychology, Drug Research and Child Health (NEUROFARBA), University of Florence, Florence, Italy.

Section of Medicinal Chemistry, Department of Neurosciences, Psychology, Drug Research and Child Health (NEUROFARBA), University of Florence, Florence, Italy.

出版信息

Front Cardiovasc Med. 2022 Sep 20;9:751499. doi: 10.3389/fcvm.2022.751499. eCollection 2022.

Abstract

Pirfenidone is a small drug with marked antifibrotic activity approved for the treatment of Idiopathic pulmonary fibrosis. Recently, its peculiar pharmacological profile has attracted attention for its potential therapeutic benefit for extra-pulmonary disorders characterized by pathological fibrosis, such as kidney, liver, and cardiac failure. A major pitfall of pirfenidone is the lack of consistent understanding of its mechanism of action, regardless of the target. In addition to the increasing attention to the role of inflammation and its mediators in several processes, a better knowledge of the variety of fibroblasts' population, of signals controlling their activation and trans-differentiation, and of crosstalk with other cell resident and non-resident cell types is needed for prevention, treatment and possibly reverse of fibrosis. This review will focus on pirfenidone's pharmacological profile and its effects on cardiac fibroblasts.

摘要

吡非尼酮是一种具有显著抗纤维化活性的小分子药物,已被批准用于治疗特发性肺纤维化。最近,其独特的药理学特性因其对以病理性纤维化为特征的肺外疾病(如肾脏、肝脏和心力衰竭)的潜在治疗益处而受到关注。吡非尼酮的一个主要缺陷是,无论其靶点如何,人们对其作用机制都缺乏一致的认识。除了炎症及其介质在多个过程中的作用越来越受到关注外,为了预防、治疗和可能逆转纤维化,还需要更好地了解成纤维细胞群体的多样性、控制其激活和转分化的信号,以及与其他驻留细胞和非驻留细胞类型的相互作用。本综述将聚焦于吡非尼酮的药理学特性及其对心脏成纤维细胞的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0382/9530045/ea8156ee8fa3/fcvm-09-751499-g0001.jpg

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