作者: J. C. McGrath , N. A. Flavahan , C. E. McKean
DOI: 10.1097/00005344-198200041-00021
关键词: Prazosin 、 Internal medicine 、 Chronotropic 、 Rauwolscine 、 Alpha-2 adrenergic receptor 、 Adrenergic receptor 、 Alpha (ethology) 、 Phenylephrine 、 Stimulation 、 Endocrinology 、 Chemistry
摘要: In pithed rats or rabbits the pressor effects of catecholamines sympathetic nerve stimulation can be reduced by "selective" antagonists alpha 1- (prazosin) 2 (rauwolscine) adrenoceptors. response to low and high doses intravenous noradrenaline were due predominantly 2- 1-adrenoceptors, respectively. With frequencies vasopressor stimulation, could blocked each antagonist, suggesting either that both receptors involved unlike those activated circulating noradrenaline. higher frequencies, prazosin responses but left a residual which not eliminated rauwolscine; this indicate "non-alpha" junctional activation; rauwolscine, on its own, increase indicating blockade prejunctional alpha-mediated feedback. rats, acid-base balance was critical for activation 2-adrenoceptors. The indicated adrenaline acts through 1-adrenoceptors at pH, influence increased as pH falls. Also, fell, phenylephrine xylazine decreased, respectively, mechanism change lies subsequent stage in excitation-contraction coupling. These results are discussed relation current hypotheses heterogeneity postjunctional