Center on Aging, UConn Health, University of Connecticut SOM, Farmington, Connecticut.
Department of Neuroscience, UConn Health, University of Connecticut SOM, Farmington, Connecticut.
Neurourol Urodyn. 2019 Nov;38(8):2121-2129. doi: 10.1002/nau.24149. Epub 2019 Aug 26.
The prevalence of urinary dysfunction increases with age, yet therapies are often suboptimal. Incomplete understanding of the linkages between system, organ, and tissue domains across lifespan remains a knowledge gap. If tissue-level changes drive the aging bladder phenotype, parallel changes should be observed across these domains. In contrast, a lack of inter-domain correlation across age groups would support the hypothesis that urinary performance is a measure of the physiologic reserve, dependent on centrally-mediated adaptive mechanisms in the aging system.
Male and female mice across four age groups underwent sequential voiding spot assays, pressure/flow cystometry, bladder strip tension studies, histology, and quantitative PCR analyses. The primary objective of this study was to test the impact of age on the cortical, autonomic, tissue functional and structural, and molecular domains, and identify inter-domain correlations among variables showing significant changes with age within these domains.
Behavior revealed diminished peripheral voiding and spot size in aged females. Cystometry demonstrated increased postvoid residual and loss of volume sensitivity, but the preservation of voiding contraction power, with almost half of oldest-old mice failing under cystometric stress. Strip studies revealed no significant differences in adrenergic, cholinergic, or EFS sensitivity. Histology showed increased detrusor and lamina propria thickness, without a change in collagen/muscle ratio. Adrb2 gene expression decreased with age. No consistent inter-domain correlations were found across age groups.
Our findings are consistent with a model in which centrally-mediated adaptive failures to aging stressors are more influential over the aging bladder phenotype than local tissue changes.
随着年龄的增长,尿功能障碍的患病率增加,但治疗方法往往并不理想。对系统、器官和组织域之间的联系在整个生命周期中尚未完全理解,这仍然是一个知识空白。如果组织水平的变化是导致衰老膀胱表型的原因,那么在这些领域中应该观察到平行的变化。相比之下,如果不同年龄组之间的域间相关性缺乏,则支持尿功能是生理储备的衡量标准的假说,这取决于衰老系统中中枢介导的适应性机制。
四个年龄组的雄性和雌性小鼠依次进行排尿斑点分析、压力/流量膀胱测压、膀胱条张力研究、组织学和定量 PCR 分析。本研究的主要目的是测试年龄对皮质、自主、组织功能和结构以及分子域的影响,并确定在这些域中与年龄相关的变量之间的域间相关性。
行为研究显示,老年雌性动物的外周排尿和斑点大小减少。测压法显示残余尿量增加和体积敏感性丧失,但排尿收缩力得到保留,几乎一半的最老年小鼠在测压应激下失败。条带研究显示肾上腺素能、胆碱能或 EFS 敏感性没有显著差异。组织学显示逼尿肌和固有层厚度增加,而胶原/肌肉比例没有变化。Adrb2 基因表达随年龄增长而降低。在不同年龄组之间没有发现一致的域间相关性。
我们的发现与以下模型一致,即中枢介导的对衰老应激的适应性失败对衰老膀胱表型的影响大于局部组织变化。