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阳离子通道 TRPV4 在膀胱内的激活可改善逼尿肌无力大鼠模型的膀胱功能。

Intravesical Activation of the Cation Channel TRPV4 Improves Bladder Function in a Rat Model for Detrusor Underactivity.

机构信息

Laboratory of Experimental Urology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium; Laboratory of Ion Channel Research, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium; TRP Channel Research Platform Leuven (TRPLe), KU Leuven, Leuven, Belgium.

Laboratory of Experimental Urology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.

出版信息

Eur Urol. 2018 Sep;74(3):336-345. doi: 10.1016/j.eururo.2018.05.020. Epub 2018 Jun 3.

Abstract

BACKGROUND

Improvement of bladder emptying by modulating afferent nerve activity is an attractive therapeutic strategy for detrusor underactivity. Transient receptor potential vanilloid 4 (TRPV4) is a sensory ion channel in urothelial cells that contribute to the detection of bladder filling.

OBJECTIVE

To investigate the potential benefit of intravesical TRPV4 agonists in a pelvic nerve injury rat model for detrusor underactivity.

DESIGN, SETTING, AND PARTICIPANTS: Female wild-type and Trpv4 knockout rats underwent sham surgery or bilateral pelvic nerve injury (bPNI). Four weeks later, rats underwent cystometry with infusion of the TRPV4 agonist GSK1016790A. Bladders were harvested for in vitro pharmacological studies, quantitative reverse polymerase chain reaction and immunohistochemistry.

OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS

Data are expressed as median ± interquartile range. Statistical comparisons were made using the Mann-Witney U test and Wilcoxon signed rank test as appropriate.

RESULTS AND LIMITATIONS

Rats with bPNI showed a phenotype characteristic of detrusor underactivity with lower-amplitude voiding contractions, decreased voiding frequency, and increased postvoid residual. Intravesical application of GSK1016790A increased voiding frequency and reduced postvoid residual in wild-type, but not Trpv4, rats. In isolated bladder strips, GSK1016790A did not induce relevant contractions, indicating that the observed improvements in bladder function are the result of increased afferent signalling through TRPV4 activation, rather than a local effect on the detrusor. The altered urinary phenotype of Trpv4 mice was not apparent in the Trpv4 rat model, suggesting species-related functional variations. Our results are limited to the preclinical setting in rodents.

CONCLUSIONS

Intravesical activation of TRPV4 improves bladder dysfunction after bPNI by increasing afferent signalling.

PATIENT SUMMARY

We demonstrate that the sensory protein transient receptor potential vanilloid 4 (TRPV4) can be targeted to improve bladder function in animals that have iatrogenic injury to the nerves innervating the bladder. Further research is required to determine whether these results can be translated to patients with an underactive bladder.

摘要

背景

通过调节传入神经活动来改善膀胱排空是治疗逼尿肌活动低下的一种有吸引力的治疗策略。瞬时受体电位香草酸 4(TRPV4)是尿路上皮细胞中的一种感觉离子通道,有助于检测膀胱充盈。

目的

在骨盆神经损伤大鼠模型中研究膀胱内 TRPV4 激动剂在逼尿肌活动低下中的潜在益处。

设计、地点和参与者:雌性野生型和 Trpv4 敲除大鼠接受假手术或双侧骨盆神经损伤(bPNI)。4 周后,大鼠进行膀胱测压,并输注 TRPV4 激动剂 GSK1016790A。采集膀胱进行体外药理学研究、定量逆转录聚合酶链反应和免疫组织化学。

结果测量和统计分析

数据表示为中位数±四分位距。使用 Mann-Whitney U 检验和 Wilcoxon 符号秩检验进行适当的统计比较。

结果和局限性

bPNI 大鼠表现出逼尿肌活动低下的特征性表型,表现为排尿收缩幅度降低、排尿频率降低和残余尿量增加。膀胱内应用 GSK1016790A 可增加野生型大鼠的排尿频率并减少残余尿量,但在 Trpv4 大鼠中无效。在分离的膀胱条中,GSK1016790A 不会引起相关收缩,这表明观察到的膀胱功能改善是通过 TRPV4 激活增加传入信号的结果,而不是对逼尿肌的局部作用。Trpv4 小鼠的改变的尿表型在 Trpv4 大鼠模型中并不明显,表明与物种相关的功能差异。我们的结果仅限于啮齿动物的临床前环境。

结论

膀胱内激活 TRPV4 通过增加传入信号改善 bPNI 后的膀胱功能障碍。

患者总结

我们证明,感觉蛋白瞬时受体电位香草酸 4(TRPV4)可以作为靶点,改善对支配膀胱的神经造成医源性损伤的动物的膀胱功能。需要进一步研究以确定这些结果是否可以转化为逼尿肌活动低下的患者。

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