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使用缓慢降解类似物α,β-亚甲基ATP诱导P2嘌呤受体脱敏:对豚鼠膀胱非肾上腺素能、非胆碱能反应的影响

The use of the slowly degradable analog, alpha, beta-methylene ATP, to produce desensitisation of the P2-purinoceptor: effect on non-adrenergic, non-cholinergic responses of the guinea-pig urinary bladder.

作者信息

Kasakov L, Burnstock G

出版信息

Eur J Pharmacol. 1982 Dec 24;86(2):291-4. doi: 10.1016/0014-2999(82)90330-2.

Abstract

alpha, beta-Methylene ATP has advantages over ATP in producing desensitisation of the P2-purinoceptor since it is degraded more slowly than ATP and does not initiate synthesis of prostaglandins. Following desensitisation of the excitatory P2-purinoceptors in the guinea-pig urinary bladder, the excitatory responses to non-adrenergic, non-cholinergic nerve stimulation were abolished, while those to acetylcholine and histamine were little affected. This result is consistent with the purinergic nerve hypothesis.

摘要

α,β-亚甲基ATP在使P2嘌呤受体脱敏方面比ATP更具优势,因为它比ATP降解得更慢,且不会引发前列腺素的合成。豚鼠膀胱中兴奋性P2嘌呤受体脱敏后,对非肾上腺素能、非胆碱能神经刺激的兴奋性反应消失,而对乙酰胆碱和组胺的反应影响不大。这一结果与嘌呤能神经假说相符。

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