Literature DB >> 7955201

Time course of coronary endothelial healing after injury due to ischemia and reperfusion.

L D Horwitz1, D Kaufman, M W Keller, Y Kong.   

Abstract

BACKGROUND: Although it has been demonstrated in short-term preparations that ischemia with early reperfusion results in coronary vascular injury manifested by abnormal endothelium-dependent relaxation and increased permeability to plasma proteins, it has not been clear whether these abnormalities are permanent or reversible. METHODS AND
RESULTS: In a canine model, regional coronary ischemia was accomplished by 1 hour of left anterior descending coronary artery ligation, and follow-up studies were performed after reperfusion for 1 hour, 48 hours, 2 weeks, or 9 weeks. Vasorelaxation was measured in vitro with preconstricted epicardial coronary artery rings subjected to increasing concentrations of the endothelium-dependent vasodilator ADP and the endothelium-independent vasodilator nitroprusside. At 1 and 48 hours of reperfusion, relaxation of rings from the ischemic reperfused artery to ADP was blunted, but relaxation to nitroprusside was normal. At 2 weeks there was a nonsignificant trend toward a blunted response to ADP in the ischemic/reperfused rings, and at 9 weeks a completely normal response to ADP was observed. Coronary microvascular permeability was assessed by measurement of protein leak index (PLI), by using a double-isotope technique with autologous radiolabeled transferrin and erythrocytes. At 1 and 48 hours of reperfusion there were substantial increases in PLI in the previously ischemic regions, indicative of increased extravascular transferrin. There was a small increase in PLI at 2 weeks but a completely normal measurement at 9 weeks. Electron microscopy of ischemic/reperfused vessels demonstrated endothelial cell swelling and other abnormalities in epicardial arteries and the microcirculation at 48 hours of reperfusion but normal endothelium at 2 weeks of reperfusion.
CONCLUSIONS: After 1 hour of regional coronary ischemia, coronary endothelial injury occurs early in reperfusion with abnormalities in epicardial coronary artery endothelium-dependent relaxation, coronary microvascular permeability, and both epicardial coronary artery and microvascular histology. This pattern of injury persists for at least 48 hours, but there is partial functional and complete histological recovery within 2 weeks and complete functional recovery within 9 weeks.

Entities:  

Mesh:

Year:  1994        PMID: 7955201     DOI: 10.1161/01.cir.90.5.2439

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  16 in total

1.  Micro- and Nanoparticles for Treating Cardiovascular Disease.

Authors:  S Suarez; A Almutairi; K L Christman
Journal:  Biomater Sci       Date:  2015-04       Impact factor: 6.843

2.  Multimodality imaging demonstrates trafficking of liposomes preferentially to ischemic myocardium.

Authors:  Michael J Lipinski; M Teresa Albelda; Juan C Frias; Stasia A Anderson; Dror Luger; Peter C Westman; Ricardo O Escarcega; David G Hellinga; Ron Waksman; Andrew E Arai; Stephen E Epstein
Journal:  Cardiovasc Revasc Med       Date:  2016-01-21

3.  Induced peroxidase and cytoprotective enzyme expressions support adaptation of HUVECs to sustain subsequent H2O2 exposure.

Authors:  Hemang Patel; Juan Chen; Mahendra Kavdia
Journal:  Microvasc Res       Date:  2015-09-25       Impact factor: 3.514

4.  Enzyme-Responsive Nanoparticles for Targeted Accumulation and Prolonged Retention in Heart Tissue after Myocardial Infarction.

Authors:  Mary M Nguyen; Andrea S Carlini; Miao-Ping Chien; Sonya Sonnenberg; Colin Luo; Rebecca L Braden; Kent G Osborn; Yiwen Li; Nathan C Gianneschi; Karen L Christman
Journal:  Adv Mater       Date:  2015-08-25       Impact factor: 30.849

5.  Ischemic preconditioning and superoxide dismutase protect against endothelial dysfunction and endothelium glycocalyx disruption in the postischemic guinea-pig hearts.

Authors:  A Beresewicz; E Czarnowska; M Maczewski
Journal:  Mol Cell Biochem       Date:  1998-09       Impact factor: 3.396

Review 6.  Adenosine-associated delivery systems.

Authors:  Mehdi Kazemzadeh-Narbat; Nasim Annabi; Ali Tamayol; Rahmi Oklu; Amyl Ghanem; Ali Khademhosseini
Journal:  J Drug Target       Date:  2015       Impact factor: 5.121

7.  Targeting the Extracellular Matrix in Traumatic Brain Injury Increases Signal Generation from an Activity-Based Nanosensor.

Authors:  Rebecca M Kandell; Julia A Kudryashev; Ester J Kwon
Journal:  ACS Nano       Date:  2021-12-06       Impact factor: 15.881

8.  Targeting delivery of Radix Ophiopogonis polysaccharide to ischemic/reperfused rat myocardium by long-circulating macromolecular and liposomal carriers.

Authors:  LiNa Wang; ChunXia Yao; Fei Wu; Xiao Lin; Lan Shen; Yi Feng
Journal:  Int J Nanomedicine       Date:  2015-09-10

9.  Increased cardiac distribution of mono-PEGylated Radix Ophiopogonis polysaccharide in both myocardial infarction and ischemia/reperfusion rats.

Authors:  ChunXia Yao; XiaoLi Shi; Xiao Lin; Lan Shen; DeSheng Xu; Yi Feng
Journal:  Int J Nanomedicine       Date:  2015-01-09

Review 10.  Targeted nanoscale therapeutics for myocardial infarction.

Authors:  Holly L Sullivan; Nathan C Gianneschi; Karen L Christman
Journal:  Biomater Sci       Date:  2020-12-23       Impact factor: 6.843

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.