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去甲肾上腺素和三磷酸腺苷对兔中耳动脉交感神经刺激反应的贡献取决于刺激参数。

The contributions of noradrenaline and ATP to the responses of the rabbit central ear artery to sympathetic nerve stimulation depend on the parameters of stimulation.

作者信息

Kennedy C, Saville V L, Burnstock G

出版信息

Eur J Pharmacol. 1986 Apr 2;122(3):291-300. doi: 10.1016/0014-2999(86)90409-7.

DOI:10.1016/0014-2999(86)90409-7
PMID:3709657
Abstract

The possibility that ATP and noradrenaline act as cotransmitters from sympathetic perivascular nerves was studied in the isolated rabbit central ear artery. Electrical stimulation of the perivascular nerves for either 1 s, or continuously until a maximum response was reached, produced frequency-dependent contractions that were sensitive to tetrodotoxin and guanethidine. Contractions to continuous stimulation were significantly greater than those to a 1 s train of stimulation. Prazosin (10(-6) M) significantly reduced, but did not abolish, all neurogenic contractions such that contractions to both a 1 s train and to continuous stimulation were now of a similar magnitude. A higher concentration of prazosin (10(-5) M) had no additional inhibitory effect on neurogenic contractions even though it further significantly inhibited contractions to exogenous noradrenaline. The greatest resistance to alpha-adrenoceptor blockade was seen at low frequencies. Desensitisation of the postjunctional P2-purinoceptor by repeated administration of alpha, beta-methylene ATP inhibited the non-adrenergic neurogenic contractions and contractions to exogenous ATP, but had no effect on contractions to exogenous noradrenaline. It is concluded that ATP and noradrenaline are excitatory cotransmitters from sympathetic perivascular nerves innervating the rabbit central ear artery. The relative contribution of each compound to neurogenic contractions of the ear artery is highly dependent on the parameters of stimulation used. Short pulse bursts (1 s) at low frequency (2-5 Hz) favour the prazosin-resistant (purinergic) component of the response.

摘要

在离体兔中耳动脉中研究了ATP和去甲肾上腺素作为交感血管周围神经共同递质的可能性。对血管周围神经进行1秒的电刺激或持续刺激直至达到最大反应,可产生频率依赖性收缩,这些收缩对河豚毒素和胍乙啶敏感。持续刺激引起的收缩明显大于1秒串刺激引起的收缩。哌唑嗪(10^(-6) M)显著降低但并未消除所有神经源性收缩,使得对1秒串刺激和持续刺激的收缩现在幅度相似。更高浓度的哌唑嗪(10^(-5) M)对神经源性收缩没有额外的抑制作用,尽管它进一步显著抑制了对外源性去甲肾上腺素的收缩。在低频时观察到对α-肾上腺素能受体阻断的最大抗性。通过重复给予α,β-亚甲基ATP使节后P2-嘌呤能受体脱敏,抑制了非肾上腺素能神经源性收缩和对外源性ATP的收缩,但对外源性去甲肾上腺素的收缩没有影响。得出的结论是,ATP和去甲肾上腺素是支配兔中耳动脉的交感血管周围神经的兴奋性共同递质。每种化合物对耳动脉神经源性收缩的相对贡献高度依赖于所使用的刺激参数。低频(2 - 5 Hz)下的短脉冲串(1秒)有利于反应中对哌唑嗪耐药(嘌呤能)的成分。

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