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利血平和6-羟基多巴胺对兔隐动脉交感神经反应中肾上腺素能和嘌呤能成分的影响。

Effects of reserpine and 6-hydroxydopamine on the adrenergic and purinergic components of sympathetic nerve responses of the rabbit saphenous artery.

作者信息

Warland J J, Burnstock G

机构信息

Department of Anatomy, University College, London.

出版信息

Br J Pharmacol. 1987 Dec;92(4):871-80. doi: 10.1111/j.1476-5381.1987.tb11393.x.

Abstract

1 The effects of reserpine and of 6-hydroxydopamine on the contractions of the rabbit isolated saphenous artery produced by stimulation of the sympathetic nerves were studied. 2 In vessels exposed to reserpine, substantial contractions to nerve stimulation were recorded despite a 95.7% reduction in the noradrenaline content of the tissue. These responses of the vessel were not significantly affected by the alpha 1-antagonist, prazosin, whereas after desensitization of the P2-purinoceptor with alpha, beta-methylene ATP, no response to nerve stimulation remained. 3 In vessels exposed to 6-hydroxydopamine, no nerve-mediated responses were observed. 4 Noradrenaline-containing nerves were observed by fluorescence histochemistry in control tissues, but were not observed in tissues treated with reserpine or 6-hydroxydopamine. 5 The potencies of ATP and histamine were not significantly affected by reserpine or 6-hydroxydopamine treatment. However, there was a slight supersensitivity to noradrenaline in reserpine-treated and 6-hydroxydopamine-treated vessels compared with that of control vessels. Prazosin was selective for alpha-adrenoceptors, while alpha, beta-methylene ATP was selective for P2-purinoceptors. 6 These results substantiate the finding that ATP and noradrenaline are sympathetic cotransmitters in the rabbit isolated saphenous artery, and demonstrate that ATP can act as a transmitter independently of noradrenaline in this vessel.

摘要
  1. 研究了利血平和6-羟基多巴胺对刺激兔离体隐动脉交感神经所产生收缩作用的影响。2. 在暴露于利血平的血管中,尽管组织中去甲肾上腺素含量降低了95.7%,但对神经刺激仍记录到明显的收缩反应。血管的这些反应不受α1拮抗剂哌唑嗪的显著影响,而在用α,β-亚甲基ATP使P2嘌呤受体脱敏后,对神经刺激不再有反应。3. 在暴露于6-羟基多巴胺的血管中,未观察到神经介导的反应。4. 通过荧光组织化学在对照组织中观察到含去甲肾上腺素的神经,但在用利血平或6-羟基多巴胺处理的组织中未观察到。5. ATP和组胺的效能不受利血平或6-羟基多巴胺处理的显著影响。然而,与对照血管相比,利血平处理和6-羟基多巴胺处理的血管对去甲肾上腺素略有超敏反应。哌唑嗪对α-肾上腺素能受体具有选择性,而α,β-亚甲基ATP对P2嘌呤受体具有选择性。6. 这些结果证实了ATP和去甲肾上腺素是兔离体隐动脉中的交感神经共同递质这一发现,并表明在该血管中ATP可以独立于去甲肾上腺素发挥递质作用。

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