Vizi E S, Ludvig N
Eur J Pharmacol. 1983 Aug 5;91(4):377-81. doi: 10.1016/0014-2999(83)90161-9.
The alpha-adrenoceptor activity of (-)-amidephrine in the isolated vas deferens of the rat was characterized. In this preparation (-)-amidephrine showed a selective activity on alpha 1-adrenoceptors, and failed to exert any effect on alpha 2-adrenoceptors. The alpha 1-adrenoceptor antagonists prazosin (pA2 8.19 and 8.48) and E-643 (pA2 8.36 and 8.25) inhibited the agonist activity of (-)-amidephrine and (-)-phenylephrine. The pA2 values obtained did not differ significantly, indicating that the two agonists exert their effect on the same receptor. The slopes of Schild plots were not significantly different from 1, suggesting that the inhibition was truly competitive in nature.
对(-)-酰胺肾上腺素在大鼠离体输精管中的α-肾上腺素能受体活性进行了表征。在此制剂中,(-)-酰胺肾上腺素对α1-肾上腺素能受体表现出选择性活性,而对α2-肾上腺素能受体未产生任何作用。α1-肾上腺素能受体拮抗剂哌唑嗪(pA2为8.19和8.48)和E-643(pA2为8.36和8.25)抑制了(-)-酰胺肾上腺素和(-)-去氧肾上腺素的激动剂活性。获得的pA2值没有显著差异,表明这两种激动剂对同一受体发挥作用。Schild图的斜率与1没有显著差异,表明这种抑制在本质上是真正竞争性的。