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作 者:Marc Irqsusi Fiona R Rodepeter Madeline Günther Andreas Kirschbaum Sebastian Vogt
机构地区:[1]Department of Heart Surgery,Universitätsklinikum Marburg and Gießen GmbH,Marburg 35043,Hesse,Germany [2]Institute of Pathology,Philipps-University Marburg,Marburg 35043,Hesse,Germany [3]Department of Heart Surgery,Cardiovascular Research Laboratory,Philipps-University Marburg,Marburg 35043,Hesse,Germany [4]Department of Visceral Surgery,University Hospital Giessen and Marburg GmbH,Marburg 35043,Hesse,Germany [5]Department of Heart Surgery,Philipps-University Marburg,Marburg 35043,Hesse,Germany
出 处:《World Journal of Experimental Medicine》2025年第2期1-11,共11页世界实验医学杂志(英文)
摘 要:Aneurysms and dissections represent some of the most serious cardiovascular diseases.The prevailing theory posits that mechanical overloading of the vessel wall is the underlying cause.Inspired by Barkhordarian et al,the authors present matrix metalloproteinases(MMPs)and their inhibitors in immunohistological analyses as contributing factors in the pathophysiology of aortic aneurysms(AA).Data analysis of MMP-1,MMP-9,tissue inhibitors of metalloproteinases(TIMPs),including TIMP-1 and TIMP-2 expression reveals a varied distribution between the adventitia and media and a non-uniform expression of the investigated markers.These elements,as key components of the extracellular matrix(ECM),indicate that the formation of AA is not solely driven by endoluminal pressure loading of the aortic wall.Instead,degenerative processes within ECM elements contribute significantly.Importantly,AA do not necessarily imply dissection.Tissue destruction,allowing blood flow entry,arises from reduced oxygen supply to the media,primarily due to incomplete capillarization or neocapillarization.
关 键 词:Matrix metalloproteinases Tissue inhibitor of metalloproteinases Acute aortic dissection Aortic aneurysm Extracellular matrix remodeling PATHOGENESIS
分 类 号:R543.1[医药卫生—心血管疾病]
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