Cooling Augments Platelet-Induced Contraction of Peripheral Arteries of the Dog
- 1 June 1984
- journal article
- research article
- Published by Frontiers Media SA in Experimental Biology and Medicine
- Vol. 176 (2) , 119-122
- https://doi.org/10.3181/00379727-176-41850
Abstract
The effect of cooling on platelet-induced contractions was studied. Rings of canine saphenous arteries were suspended for isometric tension recording in organ baths filled with aerated physiological salt solution. Norepinephrine, 5-hydroxytryptamine and autologous aggregating platelets all caused contractions that were augmented by cooling the bath content from 37.degree. to 24.degree. C. These contractions were inhibited, in a concentration-dependent manner, by the serotonergic antagonist ketanserin. The .alpha.1-adrenergic antagonist, prazosin, in concentrations causing progressive inhibition of contractions evoked by norepinephrine did not affect the response to either 5-hydroxytryptamine or platelets. Aggregating platelets were found to release 5-hydroxytryptamine in sufficient amounts to account for the observed contractions. Pretreatment of platelets with the cyclo-oxygenase inhibitor meclofenamate reduced the amount of thromboxane liberated by aggregating platelets but did not influence evoked contractions. Aggregating platelets may cause contraction of the canine saphenous artery by releasing 5-hydroxytryptamine. Apparently, cooling markedly augments contractions of peripheral arterial smooth muscle caused by aggregating platelets.This publication has 3 references indexed in Scilit:
- CHARACTERIZATION OF THE ANTIHYPERTENSIVE PROPERTIES OF KETANSERIN (R-41-468) IN RATS1982
- Effect of imidazole on renal function in unilateral ureteral-obstructed rat kidneysAmerican Journal of Physiology-Renal Physiology, 1981
- Instantaneous changes of alpha-adrenoceptor affinity caused by moderate cooling in canine cutaneous veinsAmerican Journal of Physiology-Heart and Circulatory Physiology, 1978