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Citations to this article

Reduction of sympathetic inotropic response after ischemia in dogs. Contributor to stunned myocardium.
A A Ciuffo, … , L Levin, M L Weisfeldt
A A Ciuffo, … , L Levin, M L Weisfeldt
Published May 1, 1985
Citation Information: J Clin Invest. 1985;75(5):1504-1509. https://doi.org/10.1172/JCI111854.
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Research Article

Reduction of sympathetic inotropic response after ischemia in dogs. Contributor to stunned myocardium.

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Abstract

Eight open chest dogs underwent 25 min of coronary occlusion to determine whether brief myocardial ischemia disrupts the normal myocardial inotropic response to sympathetic nervous stimulation. If so, this could represent a mechanism contributing to postischemic myocardial dysfunction. Myocardial segment shortening was measured using ultrasonic dimension crystals before and after coronary artery occlusion and reperfusion. Left ansa subclavia stimulation and systemic norepinephrine (NE) infusion were used to test the myocardial inotropic response to neural stimulation and direct exposure to the sympathetic mediator, respectively. Before coronary artery occlusion, base-line preischemic segment shortening (12.5 +/- 1.6%) (SEM) increased during both sympathetic stimulation (20.2 +/- 1.4%) and NE infusion (19.7 +/- 1.1%). The control segment responded similarly. After ischemia and reperfusion there was no significant change in heart rate, aortic or left ventricular pressures, nor changes in control segment shortening. In contrast, shortening in the postischemic segment was markedly reduced compared to baseline (4.1 +/- 2.4%), and no longer responded to sympathetic stimulation (2.4 +/- 2.8%), while responsiveness to systemic NE was maintained (12.9 +/- 2.0%), P less than 0.001, which suggested injury to the sympathetic-neural axis during the period of ischemia. This reduced response to neural stimulation was persistent for up to 2 h after reperfusion. Left atrial or intracoronary infusion of bretylium tosylate, which releases norepinephrine from nerve terminals, resulted in an immediate inotropic response in the postischemic segment, which indicated that total depletion of NE from nerve terminals during the ischemic period had not occurred. Disruption of sympathetic neural responsiveness is likely a component of the mechanism of postischemic myocardial dysfunction whenever there is appreciable sympathetic drive to the heart.

Authors

A A Ciuffo, P Ouyang, L C Becker, L Levin, M L Weisfeldt

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Total citations by year

Year: 2019 2014 2013 2012 2010 2006 2005 2003 2002 1998 1997 1996 1995 1994 1993 1992 1991 1990 1989 1988 1987 1986 Total
Citations: 1 2 1 1 1 1 2 1 2 2 2 2 5 3 4 3 5 10 3 7 4 2 64
Citation information
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Citations to this article (64)

Title and authors Publication Year
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Hibernating myocardium results in partial sympathetic denervation and nerve sprouting
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American journal of physiology. Heart and circulatory physiology 2013
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JA Fallavollita, JM Canty
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Journal of Cardiac Surgery 1994
Regional asynchrony of segmental contraction may explain the "oxygen consumption paradox" in stunned myocardium
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Basic Research in Cardiology 1993
Experimental Study of Cardiac Lymph in Myocardial Stunning
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Vascular and endovascular surgery 1993
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HM Piper, CJ Preusse
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Clinical Cardiology 1992
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Annals of Emergency Medicine 1991
The Jaundiced Heart: Evidence of Blunted Response to Positive Inotropic Stimulation
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