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从剖析纤维化途径到评估药物相互作用以减少心脏纤维化和心力衰竭。

From dissection of fibrotic pathways to assessment of drug interactions to reduce cardiac fibrosis and heart failure.

作者信息

Garoffolo Gloria, Pesce Maurizio

机构信息

Unità di Ingegneria Tissutale Cardiovascolare, Centro Cardiologico Monzino, IRCCS, Milan, Italy.

出版信息

Curr Res Pharmacol Drug Discov. 2021 May 25;2:100036. doi: 10.1016/j.crphar.2021.100036. eCollection 2021.

DOI:10.1016/j.crphar.2021.100036
PMID:34909666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8663973/
Abstract

Cardiac fibrosis is characterized by extracellular matrix deposition in the cardiac interstitium, and this contributes to cardiac contractile dysfunction and progression of heart failure. The main players involved in this process are the cardiac fibroblasts, which, in the presence of pro-inflammatory/pro-fibrotic stimuli, undergo a complete transformation acquiring a more proliferative, a pro-inflammatory and a secretory phenotype. This review discusses the cellular effectors and molecular pathways implicated in the pathogenesis of cardiac fibrosis and suggests potential strategies to monitor the effects of specific drugs designed to slow down the progression of this disease by specifically targeting the fibroblasts.

摘要

心脏纤维化的特征是细胞外基质在心脏间质中沉积,这会导致心脏收缩功能障碍和心力衰竭的进展。参与这一过程的主要细胞是心脏成纤维细胞,在促炎/促纤维化刺激存在的情况下,它们会经历完全转变,获得更具增殖性、促炎和分泌性的表型。这篇综述讨论了与心脏纤维化发病机制相关的细胞效应器和分子途径,并提出了潜在的策略,以监测旨在通过特异性靶向成纤维细胞来减缓该疾病进展的特定药物的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a02b/8663973/b1cf446c3cac/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a02b/8663973/b1cf446c3cac/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a02b/8663973/b1cf446c3cac/gr1.jpg

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2
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JACC Basic Transl Sci. 2020 Sep 28;5(9):931-945. doi: 10.1016/j.jacbts.2020.07.009. eCollection 2020 Sep.
3
Single-Cell RNA Sequencing Analysis Reveals a Crucial Role for CTHRC1 (Collagen Triple Helix Repeat Containing 1) Cardiac Fibroblasts After Myocardial Infarction.
MedComm (2020). 2023 Aug 9;4(4):e340. doi: 10.1002/mco2.340. eCollection 2023 Aug.
4
Cells and Materials for Cardiac Repair and Regeneration.用于心脏修复和再生的细胞与材料
J Clin Med. 2023 May 10;12(10):3398. doi: 10.3390/jcm12103398.
5
Role of Dopamine in the Heart in Health and Disease.多巴胺在心脏健康和疾病中的作用。
Int J Mol Sci. 2023 Mar 6;24(5):5042. doi: 10.3390/ijms24055042.
6
Investigating the possible mechanisms of pirfenidone to be targeted as a promising anti-inflammatory, anti-fibrotic, anti-oxidant, anti-apoptotic, anti-tumor, and/or anti-SARS-CoV-2.研究吡非尼酮作为一种有前途的抗炎、抗纤维化、抗氧化、抗凋亡、抗肿瘤和/或抗 SARS-CoV-2 的可能机制。
Life Sci. 2022 Nov 15;309:121048. doi: 10.1016/j.lfs.2022.121048. Epub 2022 Oct 7.
7
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6
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