Hoover D B, Hancock J C
Department of Pharmacology, Quillen-Dishner College of Medicine, East Tennessee State University, Johnson City 37614.
J Auton Nerv Syst. 1988 Sep;23(3):189-97. doi: 10.1016/0165-1838(88)90093-8.
The localization of substance P (SP) binding sites in guinea-pig heart was studied by in vitro autoradiography, and pharmacological effects of SP were examined with isolated heart preparations. Specific binding of [125I]SP was found in association with cardiac parasympathetic ganglia and some coronary arteries. No specific SP binding sites were associated with coronary veins, atria, ventricles, ascending aorta or pulmonary trunk. Local bolus injections of SP (2.5 and 25 nmol) caused a bradycardia which, in some preparations, was followed by a slight tachycardia. SP produced a prominent coronary vasodilator effect after basal perfusion pressure had been elevated by 1 microM vasopressin. The vasodilator response was probably mediated by the SP binding sites associated with the coronary arteries. Bradycardia might be elicited by binding of SP to the receptors present in the parasympathetic ganglia and subsequent release of acetylcholine. It is suggested that these effects of SP on the isolated heart could be of physiological significance.
通过体外放射自显影研究了豚鼠心脏中P物质(SP)结合位点的定位,并用离体心脏标本检测了SP的药理作用。发现[125I]SP的特异性结合与心脏副交感神经节和一些冠状动脉有关。冠状动脉静脉、心房、心室、升主动脉或肺动脉干未发现特异性SP结合位点。局部推注SP(2.5和25 nmol)引起心动过缓,在某些标本中,随后出现轻微心动过速。在1 microM血管加压素使基础灌注压升高后,SP产生显著的冠状动脉扩张作用。血管扩张反应可能由与冠状动脉相关的SP结合位点介导。心动过缓可能是由于SP与副交感神经节中存在的受体结合并随后释放乙酰胆碱引起的。提示SP对离体心脏的这些作用可能具有生理意义。