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利血平和6-羟基多巴胺的使用为兔耳动脉中嘌呤能共传递提供了证据支持。

Use of reserpine and 6-hydroxydopamine supports evidence for purinergic cotransmission in the rabbit ear artery.

作者信息

Saville V L, Burnstock G

机构信息

Department of Anatomy and Developmental Biology, University College London, U.K.

出版信息

Eur J Pharmacol. 1988 Oct 18;155(3):271-7. doi: 10.1016/0014-2999(88)90513-4.

Abstract

The relative roles of noradrenaline and ATP in the contractile response of the rabbit central ear artery following electrical stimulation of the sympathetic perivascular nerves were investigated after treatment with reserpine and 6-hydroxydopamine. In control tissues, electrical stimulation produced frequency-dependent contractile responses that were reduced, but not abolished, following incubation with the alpha 1-adrenoceptor antagonist prazosin (10(-6) M). Desensitisation of the P2X-purinoceptor by alpha,beta-methylene ATP (10(-6) M) abolished the prazosin-resistant component of the response. Tissues removed from reserpine-pretreated animals responded to electrical stimulation with small, frequency-dependent contractions, despite a dramatically reduced tissue noradrenaline content. Prazosin (10(-6) M) had no significant effect on these contractile responses. Following P2X-purinoceptor desensitisation, the neurogenic responses were virtually abolished. Tissues that had been incubated with 6-hydroxydopamine failed to respond to electrical stimulation at the parameters used in the control and reserpine-pretreated vessels. This study provides supporting evidence for the involvement of noradrenaline and ATP in sympathetic cotransmission in the rabbit central ear artery.

摘要

在用利血平和6-羟基多巴胺处理后,研究了去甲肾上腺素和ATP在电刺激交感血管周围神经后家兔中耳动脉收缩反应中的相对作用。在对照组织中,电刺激产生频率依赖性收缩反应,在用α1肾上腺素能受体拮抗剂哌唑嗪(10(-6) M)孵育后,该反应减弱但未被消除。α,β-亚甲基ATP(10(-6) M)使P2X嘌呤受体脱敏,消除了反应中对哌唑嗪耐药的成分。从利血平预处理动物身上取出的组织,尽管组织去甲肾上腺素含量显著降低,但对电刺激仍有小的、频率依赖性的收缩反应。哌唑嗪(10(-6) M)对这些收缩反应无显著影响。P2X嘌呤受体脱敏后,神经源性反应几乎完全消失。用6-羟基多巴胺孵育过的组织,在对照和利血平预处理血管所用的参数下,对电刺激无反应。本研究为去甲肾上腺素和ATP参与家兔中耳动脉交感神经共同传递提供了支持性证据。

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