TY - JOUR
T1 - Regional O2 consumption and coronary flow during beta adrenoceptor stimulation in reperfused canine myocardium
AU - Acad, B. A.
AU - Weiss, H. R.
PY - 1989
Y1 - 1989
N2 - This study was performed to assess the ability of a reperfused region to increase its flow and O2 consumption upon inotropic stimulation. Isoproterenol (5 μg/kg/min) was infused i.v. during the reperfusion phase (4 hr) after 2 hr of the left anterior descending coronary artery occlusion in anesthetized open chest dogs (n = 7). The response was compared to a similar untreated reperfused group (n = 8). Coronary blood flow was obtained with labeled microspheres. Arterial and venous O2 saturations were determined microspectrophotometrically. During reperfusion and isoproterenol infusion, significantly higher heart rate (226 ± 48 beats/min), maximum positive derivative of left ventricular pressure (3132 ± 838 mm Hg/sec) and systolic aortic blood pressure (162 ± 16 mm Hg) were recorded compared to reperfusion in the control group (133 ± 22, 1615 ± 184 and 124 ± 30, respectively). In the control group, coronary blood flow to the reperfused areas decreased from preocclusion values of 85 ± 22 and 95 ± 43 to 63 ± 45 and 47 ± 31 ml/min/100 g for the subepicardium and subendocardium, respectively. O2 extraction was increased significantly in the reperfused region and O2 consumption was similar to that in the nonoccluded area. The corresponding flow values in the treated group at the end of the reperfusion period were 272 ± 142 and 183 ± 150 ml/min/100 g, respectively. With isoproterenol, the O2 extraction was not greater than in the nonoccluded area and the O2 consumption increased about 3-fold in comparison to the control group, although the increase in the reperfused subendocardium was less. Thus, the reperfused ischemic myocardium responded to isoproterenol stimulation by increasing O2 consumption. The response to isoproterenol in terms of flow and O2 consumption appear greater in the reperfused subepicardium compared to the subendocardium.
AB - This study was performed to assess the ability of a reperfused region to increase its flow and O2 consumption upon inotropic stimulation. Isoproterenol (5 μg/kg/min) was infused i.v. during the reperfusion phase (4 hr) after 2 hr of the left anterior descending coronary artery occlusion in anesthetized open chest dogs (n = 7). The response was compared to a similar untreated reperfused group (n = 8). Coronary blood flow was obtained with labeled microspheres. Arterial and venous O2 saturations were determined microspectrophotometrically. During reperfusion and isoproterenol infusion, significantly higher heart rate (226 ± 48 beats/min), maximum positive derivative of left ventricular pressure (3132 ± 838 mm Hg/sec) and systolic aortic blood pressure (162 ± 16 mm Hg) were recorded compared to reperfusion in the control group (133 ± 22, 1615 ± 184 and 124 ± 30, respectively). In the control group, coronary blood flow to the reperfused areas decreased from preocclusion values of 85 ± 22 and 95 ± 43 to 63 ± 45 and 47 ± 31 ml/min/100 g for the subepicardium and subendocardium, respectively. O2 extraction was increased significantly in the reperfused region and O2 consumption was similar to that in the nonoccluded area. The corresponding flow values in the treated group at the end of the reperfusion period were 272 ± 142 and 183 ± 150 ml/min/100 g, respectively. With isoproterenol, the O2 extraction was not greater than in the nonoccluded area and the O2 consumption increased about 3-fold in comparison to the control group, although the increase in the reperfused subendocardium was less. Thus, the reperfused ischemic myocardium responded to isoproterenol stimulation by increasing O2 consumption. The response to isoproterenol in terms of flow and O2 consumption appear greater in the reperfused subepicardium compared to the subendocardium.
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M3 - Article
C2 - 2760843
AN - SCOPUS:0024472935
SN - 0022-3565
VL - 250
SP - 611
EP - 616
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
IS - 2
ER -