Blakeley A G, Summers R J
Br J Pharmacol. 1978 Aug;63(4):683-7. doi: 10.1111/j.1476-5381.1978.tb17283.x.
1 The competitive alpha-adrenoceptor blocking agent, piperoxan, in concentrations up to 2 x 10(-4) M, produced large dose-dependent increases in transmitter overflow from the isolated blood perfused spleen of the cat following nerve stimulation at 10 hertz. 2 At concentrations greater than 2 x 10(-4) M, piperoxan produced a rise in perfusion pressure, a contraction of the splenic capsule, and a marked dose-dependent decrease in transmitter overflow. 3 Phenoxybenzamine (10(-4) M) and desmethylimipramine (3 x 10(-5) M) produced further increases in transmitter overflow when added after piperoxan. 4 Piperoxan (5.8 to 6.6 x 10(-6) M) had no effect on the recovery of 3H in the venous blood following the close arterial infusion or injection of (3H)-(--)-noradrenaline, indicating that the drug does not inhibit uptake of the amine. 5 Piperoxan produced dose-dependent inhibition of responses of the splenic vasculature to close arterial injection of 1 microgram of (--)-noradrenaline but was much less effective at inhibiting responses to nerve stimulation. At 2 x 10(-6) M piperoxan produced a considerable reduction of the response to injected noradrenaline but potentiated the response to nerve stimulation. 6 In isolated strips of cat splenic capsule, piperoxan produced a shift to the right of the dose-response curve to noradrenaline with no change of the maximum response. There was no evidence of a postsynaptic sensitizing effect of the type observed in the rat vas deferens.
竞争性α-肾上腺素能受体阻断剂哌罗克生,在浓度高达2×10⁻⁴M时,在以10赫兹频率刺激神经后,可使猫离体血液灌注脾脏的递质溢出量出现显著的剂量依赖性增加。
当浓度大于2×10⁻⁴M时,哌罗克生可使灌注压升高、脾包膜收缩,并使递质溢出量出现显著的剂量依赖性减少。
苯氧苄胺(10⁻⁴M)和去甲丙咪嗪(3×10⁻⁵M)在哌罗克生之后添加时,可使递质溢出量进一步增加。
哌罗克生(5.8至6.6×10⁻⁶M)对动脉内近距离输注或注射(³H)-(-)-去甲肾上腺素后静脉血中³H的回收无影响,表明该药物不抑制胺的摄取。
哌罗克生对脾血管系统对动脉内近距离注射1微克(-)-去甲肾上腺素的反应产生剂量依赖性抑制,但对抑制神经刺激反应的效果要差得多。在2×10⁻⁶M时,哌罗克生可使对注射去甲肾上腺素的反应显著降低,但增强了对神经刺激的反应。
在猫脾包膜的离体条带上,哌罗克生使去甲肾上腺素剂量-反应曲线右移,最大反应无变化。没有证据表明存在大鼠输精管中观察到的那种突触后致敏作用。