首页> 外文期刊>The Journal of Urology >Urodynamic and clinical evidence of acute inhibitory effects of intravesical nociceptin/orphanin FQ on detrusor overactivity in humans: a pilot study.
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Urodynamic and clinical evidence of acute inhibitory effects of intravesical nociceptin/orphanin FQ on detrusor overactivity in humans: a pilot study.

机译:膀胱内Nociceptin / orphanin FQ对人体逼尿肌过度活跃急性抑制作用的尿动力学和临床证据:一项前瞻性研究。

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PURPOSE: Management of neurogenic incontinence is complex and available treatments are not satisfactory. Nociceptin/orphanin FQ, a recently discovered neuropeptide, has been reported to inhibit the voiding reflex in the rat. These experimental results prompted us to investigate the urodynamic and clinical effects of intravesical instillation of nociceptin/orphanin FQ in humans. MATERIAL AND METHODS: Our study involved 5 normal subjects (group 1) with a mean age of 40.4 years (range 21 to 54) and 9 patients (group 2) 40.4 years (24 to 54). All patients in group 2 presented with detrusor hyperreflexia refractory to standard therapy. They were invited to undergo a filling cystometrogram with saline solution and after 30 minutes, a new one with a solution containing 1 microM. nociceptin/orphanin FQ. The urodynamic parameters that were recorded included bladder capacity, volume threshold for the appearance of detrusor hyperreflexia and maximum bladder pressure. Clinical and urodynamic followup was performedafter 15 days. The data were statistically analyzed with 1-way analysis of variance followed by the Dunnett test for multiple comparison considered statistically significant with p <0.05. RESULTS: Intravesical instillation of 1 microM. nociceptin/orphanin FQ in group 1 did not produce significant functional changes. This infusion in group 2 produced a statistically significant increase in mean bladder capacity and volume threshold for the appearance of detrusor hyperreflexia from 164 plus or minus standard deviation (SD) 84 to 301 +/- 118 and 93 plus or minus SD 41 to 231 +/- 104 ml. (p <0.05, respectively). Mean maximum bladder pressure decreased from 79 plus or minus SD 25 to 54 +/- 44 cm. water but was not statistically significant (p = 0.19). After 15 days an absence of clinical improvement was noticed in group 2, and the urodynamic control did not show any significant changes compared to the values before nociceptin/orphanin FQ treatment. No severe symptomatic reactions were observed during infusion of 1microM. nociceptin/orphanin FQ. CONCLUSIONS: Our results demonstrate that nociceptin/orphanin FQ is able to elicit a robust inhibitory effect on voiding reflex in group 2 but not 1. The ideal dosage, route of administration of nociceptin/orphanin FQ and treatment interval are not yet established.
机译:目的:神经性尿失禁的治疗很复杂,可用的治疗方法并不令人满意。据报道,最近发现的神经肽Nociceptin / orphanin FQ可抑制大鼠的排尿反射。这些实验结果促使我们研究了Nociceptin / orphanin FQ膀胱内滴入人的尿流动力学和临床效果。材料与方法:我们的研究涉及5名正常年龄(第1组),平均年龄40.4岁(21至54岁)和9名患者(第2组)40.4岁(24至54岁)。第2组中的所有患者均表现为标准疗法难治的逼尿肌反射亢进。邀请他们接受充满盐水溶液的膀胱膀胱压描记术,30分钟后,接受含有1 microM溶液的新膀胱膀胱描记图。伤害感受肽/孤儿蛋白FQ。记录的尿动力学参数包括膀胱容量,逼尿肌反射亢进的体积阈值和最大膀胱压力。 15天后进行临床和尿动力学检查。对数据进行统计学处理,首先采用方差分析,然后进行Dunnett检验,以进行多重比较,并认为具有统计学意义,p <0.05。结果:膀胱内滴注1 microM。第1组中的痛觉敏/孤儿蛋白FQ没有产生明显的功能变化。第2组中的这种输注使逼尿肌反射亢进的平均膀胱容量和体积阈值从164上下标准偏差(SD)84到301 +/- 118和93上下SD 41到231 +产生统计学上的显着增加/-104毫升。 (分别为p <0.05)。平均最大膀胱压力从79 +/- SD 25降至54 +/- 44 cm。水,但无统计学意义(p = 0.19)。 15天后,第2组未见临床改善,并且与Nociceptin / orphanin FQ治疗之前的值相比,尿动力学控制未显示任何明显变化。输注1microM期间未观察到严重的症状反应。伤害感受素/孤儿蛋白FQ。结论:我们的结果表明,伤害感受肽/孤啡肽FQ能够对第2组的排泄反射产生强烈的抑制作用,但不能引起1组。理想的剂量,伤害感受肽/孤啡肽FQ的给药途径和治疗间隔尚未确定。

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