老年小鼠尿行为和基因表达的日调节

Danielle S Taylor, Albert A Allotey, Rachel E Fanelli, Sushumna B Satyanarayana, Sharanya S Bettadapura, Cole R Wyatt, Jason G Landen, Adam C Nelson, Emily E Schmitt, Danielle R Bruns, Nicole L Bedford
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引用次数: 0

摘要

夜尿症,定义为每晚醒来一次或多次小便,是一种普遍且负担沉重的疾病,几乎没有有效的治疗方法。虽然夜尿症的主要危险因素是高龄,但很少有临床前研究涉及老年受试者夜尿症的病理生理机制。在这里,我们使用衰老小鼠开发了夜尿症的翻译模型,并建立了一种行为范式,可以对群养动物的自愿排尿进行昼夜节律评估。我们发现,与成年对照组相比,老年小鼠的尿行为的昼夜调节受到抑制。分子分析显示,在老年小鼠肾脏和膀胱组织中,典型昼夜节律基因的昼夜表达被破坏。值得注意的是,我们发现膀胱机械感觉离子通道Piezo1的昼夜调节与年龄相关,这表明昼夜节律中断与膀胱敏感性改变之间存在潜在的联系机制。我们的研究结果揭示了昼夜节律障碍在年龄相关性夜尿症中的作用,并确定Piezo1是一个有希望的时间生物学干预治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diurnal Regulation of Urinary Behavior and Gene Expression in Aged Mice
Nocturia, defined as waking one or more times per night to urinate, is a prevalent and burdensome condition with few effective treatments. While the primary risk factor for nocturia is advanced age, few preclinical studies have addressed the pathophysiological mechanisms of nocturia in older subjects. Here, we develop a translational model of nocturia using aging mice and a behavioral paradigm that enables circadian assessment of voluntary urination in group-housed animals. We discovered dampened diurnal regulation of urinary behavior in aged mice compared to adult controls. Molecular analyses revealed disrupted diurnal expression of canonical circadian genes in aged mouse kidney and bladder tissues. Notably, we identified age-related loss of diurnal regulation of the bladder mechanosensory ion channel, Piezo1, suggesting a potential mechanism linking circadian disruption to altered bladder sensitivity. Our results reveal a role for circadian dysfunction in age-related nocturia and identify Piezo1 as a promising therapeutic target for chronobiological intervention.
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