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腺苷通过一种部分被六甲铵阻断的机制增强麻醉和箭毒化豚鼠对组胺的支气管收缩反应。

Adenosine enhances the bronchocontractile response to histamine in anaesthetized and curarized guinea pigs through a mechanism partly blocked by hexamethonium.

作者信息

Breschi M C, Nieri P, Lazzeri N, Martinotti E

机构信息

Institute of Biological Sciences, Faculty of Pharmacy, University of Pisa, Italy.

出版信息

Pharmacology. 1994 Jul;49(1):42-51. doi: 10.1159/000139215.

Abstract

The ability of adenosine to potentiate the airway narrowing induced by histamine in anaesthetized and curarized guinea pigs has been investigated in order to establish whether it could be ascribed to a modulatory activity by the nucleoside at the neuronal level. Bilateral vagotomy, atropine (2 mg/kg i.v.), and pretreatment with capsaicin (52 mg/kg s.c. 6 days before the experiment) did not result in any significant protection against the enhancement provoked by the nucleoside of the bronchocontractile effect of histamine. On the contrary, the latter was significantly reduced by the ganglionic blocking agent, hexamethonium (10 mg/kg i.v.). Moreover, the effect of adenosine on airway responsiveness to histamine was not modified in animals treated with propranolol (1 mg/kg i.v.) or guanethidine (20 mg/kg s.c. over a period of 2 days). In conclusion, current data suggest that the purine is able, in our experimental model, to potentiate the bronchospasm induced by histamine by means of a mechanism mediated, at least partly, by non-adrenergic-non-cholinergic nerves not related to capsaicin-sensitive afferent neurons.

摘要

为了确定腺苷增强组胺诱导的麻醉和箭毒化豚鼠气道狭窄的能力是否可归因于该核苷在神经元水平的调节活性,对此进行了研究。双侧迷走神经切断术、静脉注射阿托品(2 mg/kg)以及在实验前6天皮下注射辣椒素(52 mg/kg)预处理,均未对核苷增强组胺支气管收缩作用所引发的效应产生任何显著的保护作用。相反,神经节阻断剂六甲铵(静脉注射10 mg/kg)可使其显著降低。此外,在用普萘洛尔(静脉注射1 mg/kg)或胍乙啶(在2天内皮下注射20 mg/kg)处理的动物中,腺苷对气道对组胺反应性的影响未发生改变。总之,目前的数据表明,在我们的实验模型中,嘌呤能够通过至少部分由与辣椒素敏感传入神经元无关的非肾上腺素能-非胆碱能神经介导的机制,增强组胺诱导的支气管痉挛。

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