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Macrophage-stimulated cardiac fibroblast production of IL-6 is essential for TGF β/Smad activation and cardiac fibrosis induced by angiotensin II.巨噬细胞刺激心肌成纤维细胞产生白细胞介素 6 对于血管紧张素 II 诱导的 TGF-β/Smad 激活和心脏纤维化是必不可少的。
PLoS One. 2012;7(5):e35144. doi: 10.1371/journal.pone.0035144. Epub 2012 May 4.
2
Matricellular proteins in cardiac adaptation and disease.细胞基质蛋白在心脏适应和疾病中的作用。
Physiol Rev. 2012 Apr;92(2):635-88. doi: 10.1152/physrev.00008.2011.
3
Contribution of impaired mitochondrial autophagy to cardiac aging: mechanisms and therapeutic opportunities.线粒体自噬障碍在心脏衰老中的作用:机制与治疗靶点
Circ Res. 2012 Apr 13;110(8):1125-38. doi: 10.1161/CIRCRESAHA.111.246108.
4
Myocardial restoration: is it the cell or the architecture or both?心肌修复:是细胞还是结构,或者两者皆有?
Cardiol Res Pract. 2012;2012:240497. doi: 10.1155/2012/240497. Epub 2012 Feb 16.
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Inflammation in coronary artery disease and acute myocardial infarction - is the stage set for novel therapies?在冠状动脉疾病和急性心肌梗死中的炎症——为新型疗法奠定了基础?
Curr Pharm Des. 2012;18(28):4358-69. doi: 10.2174/138161212802481219.
6
Anticoagulants affect matrix metalloproteinase 9 levels in blood samples of stroke patients and healthy controls.抗凝血剂会影响中风患者和健康对照组血液样本中的基质金属蛋白酶 9 水平。
Clin Biochem. 2012 Apr;45(6):483-9. doi: 10.1016/j.clinbiochem.2012.01.028. Epub 2012 Feb 8.
7
Blood cell counts and their correlation with creatine kinase and C-reactive protein in patients with acute myocardial infarction.急性心肌梗死患者的血细胞计数及其与肌酸激酶和C反应蛋白的相关性。
Int J Clin Exp Med. 2012;5(1):50-5. Epub 2012 Jan 15.
8
Three-dimensional architecture of cardiomyocytes and connective tissues in hypertrophic cardiomyopathy: a scanning electron microscopic observation.肥厚型心肌病中心肌细胞与结缔组织的三维结构:扫描电子显微镜观察
Circulation. 2012 Feb 7;125(5):738-9. doi: 10.1161/CIRCULATIONAHA.111.054668.
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Anti-inflammatory mechanisms and therapeutic opportunities in myocardial infarct healing.心肌梗死后愈合中的抗炎机制和治疗机会。
J Mol Med (Berl). 2012 Apr;90(4):361-9. doi: 10.1007/s00109-011-0847-y. Epub 2012 Jan 7.
10
Association of neutrophil/lymphocyte ratio with long-term mortality after ST elevation myocardial infarction treated with primary percutaneous coronary intervention.中性粒细胞/淋巴细胞比值与直接经皮冠状动脉介入治疗后 ST 段抬高型心肌梗死患者长期死亡率的关系。
Chin Med J (Engl). 2010 Dec;123(23):3438-43.

基质金属蛋白酶:心肌梗死的药物靶点。

Matrix metalloproteinases: drug targets for myocardial infarction.

机构信息

San Antonio Cardiovascular Proteomics Center, The University of Texas Health Science Center, San Antonio, TX 78245, USA.

出版信息

Curr Drug Targets. 2013 Mar;14(3):276-86.

PMID:23316962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3828124/
Abstract

Myocardial infarction (MI) remains a major cause of morbidity and mortality worldwide. Rapid advances in the treatment of acute MI have significantly improved short-term outcomes in patients, due in large part to successes in preventing myocardial cell death and limiting infarct area during the time of ischemia and subsequent reperfusion. Matrix metalloproteases (MMPs) play key roles in post-MI cardiac remodeling and in the development of adverse outcomes. This review highlights the importance of MMPs in the injury and remodeling response of the left ventricle and also discusses their potential as therapeutic targets Additional pre-clinical and clinical research is needed to further investigate and understand the cardioprotective effects of MMPs inhibitors.

摘要

心肌梗死(MI)仍然是全球发病率和死亡率的主要原因。急性 MI 的治疗取得了快速进展,大大改善了患者的短期预后,这在很大程度上要归功于在缺血和随后的再灌注期间成功预防心肌细胞死亡和限制梗塞面积。基质金属蛋白酶(MMPs)在心肌梗死后心脏重构和不良结局的发展中发挥着关键作用。这篇综述强调了 MMPs 在左心室损伤和重构反应中的重要性,并讨论了它们作为治疗靶点的潜力。需要更多的临床前和临床研究来进一步研究和了解 MMPs 抑制剂的心脏保护作用。