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抗胆碱能药物抑制膀胱黏膜牵张诱发的 ATP 释放。

Inhibition of stretching-evoked ATP release from bladder mucosa by anticholinergic agents.

机构信息

Institute of Biosciences and Medicine, University of Surrey, Guildford, UK.

出版信息

BJU Int. 2012 Oct;110(8 Pt B):E397-401. doi: 10.1111/j.1464-410X.2012.10966.x. Epub 2012 Feb 28.

Abstract

OBJECTIVE

To determine whether muscarinic receptor antagonism affects stretching-induced release of ATP.

MATERIALS AND METHODS

Mucosal strips, dissected from guinea pig (male, 450g; n = 10) urinary bladders, were placed in horizontal organ baths and superfused with Ca(2+) -free Tyrode's solution. Superfusate samples were taken pre- and post- intervention (rapid stretching or relaxation) and ATP concentration was quantified using a luciferin-luciferase assay. The effect of muscarinic acetylcholine receptor antagonism on ATP release was assessed by addition of methoctramine (1 µM) and 4-DAMP (10 nM).

RESULTS

Rapid stretching (0 to 13.3 ± 1.2 mN; no. strips = 20) increased ATP in the superfusate to a median threefold increase over basal levels. After a period of equilibration, tension in the mucosal strips relaxed until it had reached a new steady-state after 60 min and stretching was repeated. In the presence of 4-DAMP (10 nM) or methoctramine (1 µM), ATP concentrations after stretching reduced to 61% or 20%, respectively. By contrast, ATP concentrations in mucosa-matched controls, perfused with vehicle, increased in response to stretching by 391% and 1500%, respectively. Rapid relaxation also stimulated ATP release. This release did not appear to be sensitive to 4-DAMP or methoctramine.

CONCLUSIONS

An alteration of resting mucosal tension is the key determinant of ATP release, as ATP is released from the mucosa in response to both stretching and relaxation. Muscarinic receptor antagonism inhibits stretching-evoked ATP release from bladder mucosa, suggesting that anticholinergic agents used to treat human lower urinary tract pathologies act on urothelial muscarinic receptors.

摘要

目的

确定毒蕈碱受体拮抗作用是否影响牵张诱导的 ATP 释放。

材料和方法

从豚鼠(雄性,450g;n = 10)的尿囊中分离出黏膜条带,置于水平器官浴中并用无 Ca(2+) 的 Tyrode 溶液灌流。在干预前(快速牵张或松弛)和干预后(快速牵张或松弛)采集灌流液样本,并使用荧光素-荧光素酶测定法定量 ATP 浓度。通过加入甲硫酸新斯的明(1 µM)和 4-DAMP(10 nM)评估毒蕈碱乙酰胆碱受体拮抗作用对 ATP 释放的影响。

结果

快速牵张(0 至 13.3 ± 1.2 mN;条带数 = 20)使灌流液中的 ATP 增加至基础水平的三倍。经过一段时间的平衡后,黏膜条带的张力松弛,直到 60 分钟后达到新的稳定状态并再次牵张。在 4-DAMP(10 nM)或甲硫酸新斯的明(1 µM)存在的情况下,牵张后 ATP 浓度分别降低至 61%或 20%。相比之下,用载体灌流的黏膜匹配对照物的 ATP 浓度在牵张时分别增加了 391%和 1500%。快速松弛也刺激了 ATP 的释放。这种释放似乎对 4-DAMP 或甲硫酸新斯的明不敏感。

结论

静息黏膜张力的改变是 ATP 释放的关键决定因素,因为 ATP 是在黏膜对牵张和松弛的反应中释放的。毒蕈碱受体拮抗作用抑制膀胱黏膜牵张诱导的 ATP 释放,表明用于治疗人类下尿路疾病的抗胆碱能药物作用于尿路上皮毒蕈碱受体。

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