Effects of Inotropic Drugs on Mechanical Function and Oxygen Balance in Postischemic Canine Myocardium: Comparison of Dobutamine, Epinephrine, Amrinone, and Calcium Chloride.
10.3346/jkms.2005.20.5.732
- Author:
Kyung Yeon YOO
1
;
Hyeun KIM
;
Cheol Won JEONG
;
Heon Chang PARK
;
Hong Beom BAE
;
Jong Un LEE
Author Information
1. Department of Anesthesiology, Chonnam National University Medical School, Gwangju, Korea. kyyoo@chonnam.chonnam.ac.kr
- Publication Type:Original Article ; Comparative Study
- Keywords:
Heart;
Coronary Circulation;
Inotropic;
Reperfusion Injury;
Animal Experimentation;
Dogs;
Dobutamine;
Amrinone;
Calcium Chloride;
Epinephrine
- MeSH:
Amrinone/administration and dosage;
Animals;
Calcium Chloride/administration and dosage;
Cardiotonic Agents/*administration and dosage;
Comparative Study;
Dobutamine/administration and dosage;
Dogs;
Dose-Response Relationship, Drug;
Epinephrine/administration and dosage;
Female;
Male;
Myocardial Contraction/*drug effects;
Myocardial Stunning/*drug therapy/etiology/*physiopathology;
Oxidation-Reduction/drug effects;
Oxygen Consumption/*drug effects;
Reperfusion Injury/complications/*drug therapy/*physiopathology;
Treatment Outcome
- From:Journal of Korean Medical Science
2005;20(5):732-739
- CountryRepublic of Korea
- Language:English
-
Abstract:
Brief ischemic episodes that induce myocardial and coronary endothelial dysfunction may alter the responses to inotropic drugs. To determine the effects of inotropic drugs in stunned myocardium, the coronary blood flow (CBF), myocardial oxygen consumption (MVO2), and regional mechanical function in response to intracoronary dobutamine, epinephrine, amrinone, and calcium chloride (CaCl2) were measured before (normal) and 30 min after a 15-min-period occlusion of the left anterior descending artery (stunned) in an open-chest canine model. Percent segment shortening (%SS) and post-systolic shortening (%PSS) were determined. Myocardial extraction of oxygen (EO2) and lactate (E(lac)) was calculated. The inotropic drugs increased %SS, CBF, and MVO2 in normal myocardium. Epinephrine and amrinone decreased, while dobutamine and CaCl2 did not affect EO2. The ischemia and reperfusion itself significantly reduced %SS and E(lac), and increased %PSS. In stunned myocardium, the responses to inotropic drugs were not significantly altered, except that they progressively reduced %PSS and epinephrine did not affect EO2. These findings indicate that a brief episode of ischemia does not affect the mechanical and metabolic coronary flow responses to inotropic drugs, although it abolishes direct vasodilator responses to epinephrine.
