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哌罗克生对猫离体血液灌注脾脏中去甲肾上腺素摄取及递质释放的影响。

The effects of piperoxan on uptake of noradrenaline and overflow of transmitter in the isolated blood perfused spleen of the cat.

作者信息

Blakeley A G, Summers R J

出版信息

Br J Pharmacol. 1978 Aug;63(4):683-7. doi: 10.1111/j.1476-5381.1978.tb17283.x.

Abstract

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.

摘要
  1. 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。

  2. 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。

  3. 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。

  4. 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。

  5. 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。

  6. 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。

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本文引用的文献

1
Observations on the isolated vas deferens.对离体输精管的观察
Br J Pharmacol Chemother. 1963 Apr;20(2):299-306. doi: 10.1111/j.1476-5381.1963.tb01469.x.
3
Postnatal development of the mechanical response of the isolated rat vas deferens to nerve stimulation.
Acta Physiol Scand. 1972 Feb;84(2):217-23. doi: 10.1111/j.1748-1716.1972.tb05172.x.
5
Effects of phenoxybenzamine on transmitter release and effector response in the isolated portal vein.
J Pharm Pharmacol. 1972 Feb;24(2):161-4. doi: 10.1111/j.2042-7158.1972.tb08954.x.
6
Perfusion of the spleen with blood containing prostaglandin E1: transmitter liberation and uptake.
Proc R Soc Lond B Biol Sci. 1969 Dec 23;174(1036):281-92. doi: 10.1098/rspb.1969.0094.

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