Wake Forest Institute for Regenerative Medicine, Winston-Salem, North Carolina, USA.
J Urol. 2010 Jul;184(1):378-85. doi: 10.1016/j.juro.2010.03.004. Epub 2010 May 20.
The prevalence of bladder dysfunctions increases with age. In humans it is difficult to separate changes related to exogenous factors from those directly related to the aging process. Some confounding variables can be avoided by studying age related changes in an animal model. We evaluated the impact of age on bladder function in vivo and in vitro, and characterized the corresponding morphological changes.
Young (4 to 6 months old) and old (older than 28 to 30 months) male Fischer/Brown Norway rats were used in the study. Cystometric studies were done in conscious, freely moving rats. After cystometry tissue strips from the bladder body were used in in vitro studies of muscarinic receptor activation and electrical field stimulation, and histological examination.
Old rats had higher bladder weight than young rats but the bladder-to-body weight ratio did not change. We noted significant age related differences in 8 of 10 cystometric parameters. Old rats had increased bladder capacity, post-void residual volume, micturition volume and frequency, baseline and intermicturition pressure, and spontaneous activity but decreased micturition pressure. Bladder strip responses to carbachol and electrical field stimulation were significantly lower in old than in young rats. Histological examination revealed urothelial thinning, lower muscle mass and higher collagen content in the bladders of old vs young rats.
Physiological aging alters bladder function in male rats even when external factors remain constant. Thus, in old rats bladder capacity, post-void residual urine and spontaneous activity are higher, and responses to muscarinic receptor stimulation and electrical field stimulation are lower than in young rats. Such changes correspond to findings in aging human bladders, supporting the view that the Fischer/Brown Norway rat is a useful model in which to study age related bladder function changes.
膀胱功能障碍的患病率随年龄增长而增加。在人类中,很难将与外源性因素相关的变化与直接与衰老过程相关的变化区分开来。通过在动物模型中研究与年龄相关的变化,可以避免一些混杂变量。我们评估了年龄对体内和体外膀胱功能的影响,并对相应的形态变化进行了特征描述。
本研究使用了年轻(4 至 6 个月大)和年老(大于 28 至 30 个月大)雄性 Fischer/Brown Norway 大鼠。在清醒、自由活动的大鼠中进行了膀胱测压研究。在膀胱体组织条带进行了体外研究,以研究毒蕈碱受体激活和电刺激,以及组织学检查。
老年大鼠的膀胱重量高于年轻大鼠,但膀胱与体重的比值没有变化。我们注意到 10 个膀胱测压参数中的 8 个与年龄相关的显著差异。老年大鼠的膀胱容量、排尿后残余尿量、排尿量和频率、基础压和排尿间歇压以及自发性活动增加,但排尿压降低。与年轻大鼠相比,老年大鼠的膀胱条带对卡巴胆碱和电刺激的反应明显降低。组织学检查显示,与年轻大鼠相比,老年大鼠的膀胱上皮变薄,肌肉质量较低,胶原含量较高。
即使外部因素保持不变,生理衰老也会改变雄性大鼠的膀胱功能。因此,与年轻大鼠相比,老年大鼠的膀胱容量、排尿后残余尿量和自发性活动更高,对毒蕈碱受体刺激和电刺激的反应更低。这些变化与衰老人类膀胱的发现一致,支持 Fischer/Brown Norway 大鼠是研究与年龄相关的膀胱功能变化的有用模型的观点。