Wróbel Andrzej, Rechberger Tomasz
Second Department of Gynecology, Medical University of Lublin, Lublin, Poland.
Neurourol Urodyn. 2017 Mar;36(3):580-588. doi: 10.1002/nau.22978. Epub 2016 Feb 16.
The objective of the study was to evaluate the efficacy and safety of the combined treatment with the β AR agonist and ROCK inhibitor in the rat model of detrusor overactivity induced by retinyl acetate instillation.
The ROCK inhibitor (GSK 269962) and/or the β AR agonist (BRL 37344) were administered in single doses and a cystometry was carried out, along with a 24 hr measurement of cardiovascular parameters and diuresis.
The combined use of GSK 269962 and BRL 37344 in doses ineffective in monotherapies, ameliorated DO. An increase was found in voided volume, voiding efficiency, volume threshold, intercontraction interval, bladder compliance, and volume threshold to elicit nonvoiding contractions, accompanied by a decrease in basal pressure, threshold pressure, detrusor overactivity index, nonvoiding contractions amplitude, and frequency. The combination therapy in question proved to have no effect on micturition voiding pressure, post-void residual, bladder contraction duration, or relaxation time. A 24 hr observation of female rats who received GSK 269962 and/or BRL 37344 did not show any significant changes in urine production. BRL 37344 increased heart rate and blood pressure proportionately to the applied dose. The assessment of the combined treatment with GSK 269962 and BRL 37344 revealed a significant drop of cardiovascular parameters when compared to the rats which only received BRL 37344.
The combined use of β AR agonists and ROCK inhibitors may improve overactive bladder treatment efficacy and minimize side effects.
This polytherapy appears to improve urine storage with no impairment of voiding function. Neurourol. Urodynam. 36:580-588, 2017. © 2016 Wiley Periodicals, Inc.
本研究的目的是评估β肾上腺素能受体(β AR)激动剂与Rho激酶(ROCK)抑制剂联合治疗醋酸视黄酯灌注诱导的逼尿肌过度活动大鼠模型的疗效和安全性。
单次给予ROCK抑制剂(GSK 269962)和/或β AR激动剂(BRL 37344),并进行膀胱测压,同时对心血管参数和利尿进行24小时测量。
GSK 269962和BRL 37344联合使用,剂量在单一疗法中无效,但改善了逼尿肌过度活动。发现排尿量、排尿效率、容量阈值、收缩间期、膀胱顺应性以及引发非排尿性收缩的容量阈值增加,同时基础压力、阈值压力、逼尿肌过度活动指数、非排尿性收缩幅度和频率降低。所讨论的联合疗法对排尿压力、排尿后残余尿量、膀胱收缩持续时间或舒张时间没有影响。对接受GSK 269962和/或BRL 37344的雌性大鼠进行24小时观察,未发现尿量有任何显著变化。BRL 37344使心率和血压与给药剂量成比例增加。与仅接受BRL 37344的大鼠相比,对GSK 269962和BRL 37344联合治疗的评估显示心血管参数显著下降。
β AR激动剂和ROCK抑制剂联合使用可能提高膀胱过度活动症的治疗效果并使副作用最小化。
这种联合治疗似乎可改善尿液储存功能而不损害排尿功能。《神经泌尿学与尿动力学》36:580 - 588,2017年。© 2016威利期刊公司