Department of Pathophysiology, Medical College, Jagiellonian University, Czysta 18 Street, Cracow, Poland.
Can J Physiol Pharmacol. 2010 Sep;88(9):899-906. doi: 10.1139/y10-072.
Hyperosmolar factors induce the neurogenic inflammatory response, leading to bladder overactivity (OAB). The aim of the study was to compare the bladder motor activity in a hyperosmolar and acute cyclophosphamide (CYP)-induced model of OAB. Furthermore, we set our sights on defining the most physiological model of OAB in experimental practice. Forty-two female rats were divided randomly into 5 groups. All animals underwent cystometry with the usage of isotonic saline or saline of increasing concentration. Acute chemical cystitis was induced by CYP to elicit OAB. The following cystometric parameters were analyzed: basal pressure, threshold pressure, micturition voiding pressure, intercontraction interval, compliance, functional bladder capacity, motility index, and detrusor overactivity index. CYP and hypertonic saline solutions induced OAB. Having been compared with CYP OAB, none of the rats infused with hypertonic solution exhibited macroscopic signs of bladder inflammation. The comparison of CYP and hyperosmolar models of OAB revealed that the greatest similarity existed between the 2080 mOsm/L OAB model and the acute CYP-induced model. We postulate that the 2080 mOsm/L model of OAB can be established as being a less invasive and more physiological model when compared with the CYP-induced OAB model. Additionally, it may also be a more reliable experimental tool for evaluating novel therapeutics for OAB as compared with CYP-induced models.
高渗因素诱导神经源性炎症反应,导致膀胱过度活动症(OAB)。本研究旨在比较高渗和急性环磷酰胺(CYP)诱导的 OAB 模型中的膀胱运动活性。此外,我们旨在确定实验实践中最生理的 OAB 模型。42 只雌性大鼠随机分为 5 组。所有动物均进行膀胱测压,使用等渗盐水或浓度递增的盐水。用 CYP 诱发急性化学性膀胱炎以诱发 OAB。分析以下膀胱测压参数:基础压、阈压、排尿排空压、收缩间期、顺应性、功能性膀胱容量、运动指数和逼尿肌过度活动指数。CYP 和高渗盐水溶液均可诱导 OAB。与 CYP-OAB 相比,用高渗溶液灌注的大鼠均未出现膀胱炎症的宏观征象。CYP 和高渗性 OAB 模型的比较表明,2080 mOsm/L 的 OAB 模型与急性 CYP 诱导的模型之间存在最大的相似性。我们假设,与 CYP 诱导的 OAB 模型相比,2080 mOsm/L 的 OAB 模型可以作为一种侵入性更小、更生理的模型。此外,与 CYP 诱导的模型相比,它也可能成为评估 OAB 新型治疗药物的更可靠的实验工具。