Sidler Martin, Aitken Karen, Jiang Janet, Bijos Dominika, Belik Jaques, Bägli Darius J
Division of Urology, The Hospital for Sick Children, Toronto, ON, Canada; Institute of Medical Science, and Department of Surgery, University of Toronto, Toronto, ON, Canada.
Research Institute, Division of Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Urology. 2017 Jul;105:208.e1-208.e9. doi: 10.1016/j.urology.2017.03.032. Epub 2017 Mar 30.
To develop and evaluate a novel technique modeling partial bladder outlet obstruction (pBOO) using a nerve-sparing mid-urethral obstruction (NeMO) approach.
Female unoperated rats were compared to rats after NeMO, NeMO sham, proximal urethral (PU) obstruction, or PU sham. Residual volume, bladder capacity, voiding volume, and bladder mass were recorded; the contractile characteristics of isolated bladder strips were also analyzed. Additionally, we quantitated nerve fibers at the bladder neck as well as the extracellular matrix in the bladder wall.
NeMO yields a more predictable degree of obstruction vs PU, causes no animal mortality, and is easy to release. NeMO also results in a more moderate increase in bladder mass commensurate with human disease vs the exaggerated response to PU, and does not lead to the excessive bladder dilation observed after PU while showing increased residual urine and fibrosis over time, thus closely modeling human pBOO pathophysiology. Importantly, PU shams significantly incite both an undesirable mass increase as well as bladder dysfunction, correlating with a denervation injury making them unsuitable as controls when modeling a non-neurogenic pBOO. The bladder physiology and structure of NeMO-sham animals were indistinguishable from those of unoperated controls. The low complication rate and low variability of NeMO also can be applied to mice, opening the pBOO field to the full spectrum of transgenic manipulation.
NeMO is a pathophysiologically accurate modeling approach, with low variability and mortality, and newly paves the way for realistic and robust interpretation of omics and sequencing analytical methodologies. We therefore suggest NeMO as a new standard model when investigating pBOO.
开发并评估一种使用保留神经的尿道中段梗阻(NeMO)方法模拟部分膀胱出口梗阻(pBOO)的新技术。
将未手术的雌性大鼠与接受NeMO、NeMO假手术、近端尿道(PU)梗阻或PU假手术的大鼠进行比较。记录残余尿量、膀胱容量、排尿量和膀胱质量;还分析了离体膀胱条的收缩特性。此外,我们对膀胱颈部的神经纤维以及膀胱壁中的细胞外基质进行了定量分析。
与PU相比,NeMO产生的梗阻程度更可预测,不会导致动物死亡,且易于解除梗阻。与对PU的过度反应相比,NeMO还会使膀胱质量适度增加,与人类疾病相符,并且不会导致PU后出现的过度膀胱扩张,同时随着时间的推移会出现残余尿量增加和纤维化,从而紧密模拟人类pBOO的病理生理学。重要的是,PU假手术会显著引发不良的质量增加和膀胱功能障碍,这与去神经损伤相关,使其在模拟非神经源性pBOO时不适合作为对照。NeMO假手术动物的膀胱生理学和结构与未手术对照动物无异。NeMO的低并发症率和低变异性也可应用于小鼠,为全方位的转基因操作开辟了pBOO领域。
NeMO是一种病理生理学上准确的建模方法,变异性和死亡率低,为组学和测序分析方法的现实而有力的解释新辟了道路。因此,我们建议在研究pBOO时将NeMO作为一种新的标准模型。