EFFECTS OF ACETYLCHOLINE ON LARGE AND SMALL CORONARY-ARTERIES IN CONSCIOUS DOGS
- 1 January 1983
- journal article
- research article
- Vol. 225 (3) , 764-769
Abstract
The effects of acetylcholine, 10 .mu.g/kg i.v., were examined in 9 conscious dogs on measurements of left ventricular pressure, dP/dt [change in pressure with time], aortic pressure, heart rate, coronary blood flow, left circumflex external coronary arterial diameter, arterial and coronary sinus O2 content and calculations of late diastolic coronary resistance and left circumflex internal coronary cross-sectional area. In the absence of autonomic blockade, acetylcholine induced in conscious dogs a rapid, transient response characterized by hypotension and peak increases in coronary blood flow (+135 .+-. 14%) and coronary sinus O2 content (+5.0 .+-. 0.5 volume percent) and decreases in late diastolic coronary resistance (-65 .+-. 3%). The peak large coronary arterial effects were observed 60 s later at a time when arterial pressure, left ventricular end-diastolic pressure, left ventricular dP/dt and heart rate were not significantly different from control. At this time, large coronary cross-sectional area was increased by 36 .+-. 4%, whereas late diastolic coronary resistance was not significantly different from control. .beta.-Adrenergic or combined .alpha.- and .beta.- adrenergic receptor blockade did not alter the responses significantly. The effects were abolished by muscarinic blockade with atropine methylbromide, 0.1 mg/kg. Acetylcholine dilates large coronary arteries as well as coronary resistance vessels. These effects are independent of metabolic and adrenergic mechanisms, and are mediated by muscarinic receptors, inasmuch as the effects are abolished by prior muscarinic receptor blockade.This publication has 2 references indexed in Scilit:
- Regulation of large coronary arteries by increases in myocardial metabolic demands in conscious dogs.Circulation Research, 1981
- Transmural distribution of blood flow during activation of coronary muscarinic receptorsAmerican Journal of Physiology-Heart and Circulatory Physiology, 1981