首页> 外文期刊>Urology >Amiloride-sensitive ion channels in urinary bladder epithelium involved in mechanosensory transduction by modulating stretch-evoked adenosine triphosphate release.
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Amiloride-sensitive ion channels in urinary bladder epithelium involved in mechanosensory transduction by modulating stretch-evoked adenosine triphosphate release.

机译:膀胱上皮中对氨氯溴化物敏感的离子通道,通过调节拉伸诱发的三磷酸腺苷的释放而参与机械感觉转导。

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OBJECTIVES: To examine the possibility that mechanosensitive ion channels, including epithelial Na+ channels (ENaC), are implicated in mechanosensory transduction of the rat urinary bladder. METHODS: Cystometry with continuous infusion was performed to investigate the effect of intravesically perfused amiloride (a blocker of ENaC) on micturition reflex in urethane-anesthetized female rats. Bladder strips with or without epithelium suspended in organ bath were subjected to varying degrees of mechanical stretch (up to 50%). A luciferin-luciferase assay was used to quantify the change of stretch-evoked adenosine triphosphate (ATP) release by amiloride. The ENaC gene expression was assessed by reverse transcriptase-polymerase chain reaction. The expression and localization of ENaC proteins was examined using immunofluorescent staining. RESULTS: The intravesical perfusion of 1 mM amiloride significantly reduced the frequency of reflex voiding during bladder filling. This effect of amiloride was reversible by washing out the drug. The peak amplitude of micturition pressure was not affected by amiloride. The stretch-evoked ATP release, most of which (more than 90%) came from epithelial layer, was greatly diminished by 1 mM amiloride (from 443 to a 22% increase from basal level at 50% stretch of the original length). The alpha, beta, and gamma-ENaC subunit proteins and genes were expressed in the rat bladder epithelium. CONCLUSIONS: The amiloride-sensitive mechanosensitive channel, including ENaC, expressed in the rat bladder epithelium might be involved in the mechanosensory transduction mechanism by controlling stretch-evoked ATP release.
机译:目的:探讨机械敏感性离子通道(包括上皮Na +通道(ENaC))参与大鼠膀胱机械感觉转导的可能性。方法:连续输注膀胱镜检查以研究经膀胱灌注的阿米洛利(ENaC的阻滞剂)对尿烷麻醉雌性大鼠排尿反射的影响。对有或没有上皮悬浮在器官浴中的膀胱条进行不同程度的机械拉伸(最多50%)。使用萤光素-萤光素酶测定法定量阿米洛利引起的牵张性三磷酸腺苷(ATP)释放的变化。通过逆转录酶-聚合酶链反应评估ENaC基因表达。使用免疫荧光染色检查ENaC蛋白的表达和定位。结果:1 mM阿米洛利的膀胱内灌注显着减少了膀胱充盈期间反射性排尿的频率。阿米洛利的这种作用通过洗去药物是可逆的。排尿压的峰值幅度不受阿米洛利的影响。拉伸诱发的ATP释放(其中大部分(超过90%)来自上皮层)被1 mM阿米洛利大大降低(在原始长度的50%拉伸下,从基础水平从443增加到22%)。 α,β和γ-ENaC亚基蛋白和基因在大鼠膀胱上皮中表达。结论:在大鼠膀胱上皮中表达的阿米洛利敏感的机械敏感通道,包括ENaC,可能通过控制拉伸诱发的ATP释放而参与了机械感觉转导机制。

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