Literature DB >> 15451798

Relation of nonperfused myocardial volume and surface area to left ventricular performance in coronary microembolization.

Nasser M Malyar1, Lilach O Lerman, Mario Gössl, Patricia E Beighley, Erik L Ritman.   

Abstract

BACKGROUND: After occlusion of an epicardial artery, left ventricular (LV) dysfunction is closely related to the volume of nonperfused myocardium (NPM). The impact of coronary microembolization (ME) on LV function, however, is larger relative to the total volume of NPM. We hypothesized that the total surface area (SA), rather than the total volume, of NPM is the major determinant of ME-induced LV dysfunction. METHODS AND
RESULTS: We injected microspheres of 10-, 30-, or 100-microm diameter at each of 3 doses selectively into the left anterior descending coronary artery of 48 anesthetized pigs. Electron beam computed tomography (CT) was used to measure regional myocardial perfusion and changes in LV wall thickening (DeltaWT) and stroke volume (DeltaSV) after ME. At postmortem, a transmural "biopsy" of 1 to 2 cm3 of embolized myocardium was imaged by micro-CT, resulting in 3D images that provided volumes and SAs of the individual nonperfused foci. Additionally, in 9 pigs, creatine phosphokinase (CK) activity in embolized myocardium was measured as an index of washout of substances from the NPM. After ME, DeltaWT, DeltaSV, and CK washout were correlated more closely with the total SA (r=0.95, P<0.001; r=0.68, P<0.01; and r=0.88, P=0.01, respectively) than with the total NPM volume (r=0.59, P>0.05; 0.46, P>0.05; and r=0.69, P=0.04, respectively).
CONCLUSIONS: After coronary ME, LV dysfunction is more closely related to the total SA than to the total volume of nonperfused microregions in the myocardium.

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Year:  2004        PMID: 15451798     DOI: 10.1161/01.CIR.0000143631.15077.0F

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


  6 in total

1.  Relationship between surface area of nonperfused myocardium and extravascular extraction of contrast agent following coronary microembolization.

Authors:  Nasser M Malyar; Lilach O Lerman; Mario Gössl; Patricia E Beighley; Erik L Ritman
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-05-04       Impact factor: 3.619

2.  Mechanism of programmed cell death factor 4/nuclear factor-κB signaling pathway in porcine coronary micro-embolization-induced cardiac dysfunction.

Authors:  Qiang Su; Lang Li; Jiangyou Wang; You Zhou; Yangchun Liu
Journal:  Exp Biol Med (Maywood)       Date:  2015-03-13

3.  Myocardial microinfarction after coronary microembolization in swine: MR imaging characterization.

Authors:  Marcus Carlsson; Mark Wilson; Alastair J Martin; Maythem Saeed
Journal:  Radiology       Date:  2009-01-21       Impact factor: 11.105

Review 4.  Spontaneous and procedural plaque embolisation in native coronary arteries: pathophysiology, diagnosis, and prevention.

Authors:  Giovanni Luigi De Maria; Niket Patel; George Kassimis; Adrian P Banning
Journal:  Scientifica (Cairo)       Date:  2013-12-19

Review 5.  A fresh look at coronary microembolization.

Authors:  Petra Kleinbongard; Gerd Heusch
Journal:  Nat Rev Cardiol       Date:  2021-11-16       Impact factor: 49.421

6.  Downregulation of miR-181a-5p alleviates oxidative stress and inflammation in coronary microembolization-induced myocardial damage by directly targeting XIAP.

Authors:  You Zhou; Man-Yun Long; Zhi-Qing Chen; Jun-Wen Huang; Zhen-Bai Qin; Lang Li
Journal:  J Geriatr Cardiol       Date:  2021-06-28       Impact factor: 3.327

  6 in total

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