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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Urothelial acetylcholine involvement in ATP-induced contractile responses of the rat urinary bladder
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Urothelial acetylcholine involvement in ATP-induced contractile responses of the rat urinary bladder

机译:尿路上皮乙酰胆碱参与大鼠膀胱的ATP诱导的收缩响应

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摘要

Abstract Both acetylcholine and adenosine 5’-triphosphate (ATP) are released from the urothelium. In in vivo experiments ATP has been shown to evoke contractile responses that are significantly reduced by atropine. Currently, we aimed to examine the cholinergic part of the ATP-evoked contractile response of normal and inflamed (cyclophosphamide-treated rats) bladders. A whole bladder preparation that enabled drug administration either outside or inside the urinary bladder was used. The responses were examined in bladders from control and cyclophosphamide-treated rats that were either intact or urothelium-denuded. The expression of choline acetyltransferase and carnitine acetyltransferase were examined by Western blotting of normal and inflamed bladders. Methacholine evoked larger contractions when administered to the outside of the bladder in comparison to instillation. For ATP, an opposite trend emerged. While atropine substantially reduced the ATP-induced responses at internal administration (7.4±1.1 and 3.7±0.9 mN at 10 ?3 M; n=13; P0.001), it had no effect when administered outside the bladder. The removal of the urothelium caused a similar reduction of the responses to internal administration of ATP as caused by atropine. In cyclophosphamide-treated rats, neither atropine nor urothelium-denudation had any effect on the ATP-evoked responses. No changes in the expressions of the acetylcholine synthesising enzymes were observed. The current study shows that ATP induces a release of urothelial acetylcholine that contributes to the purinergic contractile response in the rat urinary bladder. This atropine-sensitive part of the purinergic contractile response is absent in the inflamed bladder. This may be one pathological mechanism involved in bladder dysfunction.
机译:摘要乙酰胆碱和腺苷5'-三磷酸(ATP)从尿浆中释放。在体内实验中,已显示ATP以引起阿托品显着降低的收缩反应。目前,我们旨在检查正常和发炎的ATP诱发的收缩响应的胆碱能部分(环磷酰胺处理的大鼠)膀胱。使用膀胱外部或尿膀胱内或内部的药物施用的全膀胱制剂。在具有完整或尿溶质的对照和环膦酰胺处理的大鼠中,在膀胱中检查反应。通过蛋白质印迹进行正常和发炎的膀胱检查胆碱乙酰转移酶和肉碱乙酰转移酶的表达。与滴注相比,甲素在膀胱外部施用时诱发更大的收缩。对于ATP,出现了相反的趋势。虽然阿托品大致减少了内部施用的ATP诱导的响应(7.4±1.1和3.7±0.9mn,而10?3米; n = 13; p <0.001),当膀胱外施用时它没有效果。去除尿路鞘升高导致与阿托品引起的ATP内部施用的反应相似。在环膦酰胺处理的大鼠中,阿托品和尿溶质脱氢管没有对ATP诱发的反应有任何影响。没有观察到乙酰胆碱合成酶的表达的变化。目前的研究表明,ATP诱导尿液乙酰胆碱的释放,其有助于大鼠膀胱中的嘌呤能收缩响应。在发炎的膀胱中不存在这种嘌呤能收缩响应的阿托嘌呤敏感部分。这可能是膀胱功能障碍中涉及的一种病理机制。

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