West Eliza G, Sellers Donna J, Chess-Williams Russ, McDermott Catherine
Centre for Urology Research, Faculty of Health Sciences and Medicine, Bond University, Robina, QLD, Australia.
Front Physiol. 2020 Mar 20;11:247. doi: 10.3389/fphys.2020.00247. eCollection 2020.
Psychological stress is associated with bladder dysfunction, however, the local bladder mechanisms affected are not well understood. This study aimed to determine how psychological stress, caused by social defeat or witness trauma, affects voiding behavior and bladder function. Pairs of male C57Bl/6J mice were placed in a custom-made plexiglass chamber with an aggressor ARC(S) mouse for 1 h/day for 10 days. The social defeat mouse was in physical contact with the aggressor, while the witness was physically separated but could observe interactions between its cage-mate and the aggressor. Age matched control pairs were used for comparison. Voiding analysis was conducted periodically over the 10 days. An whole bladder preparation was used to assess functional changes after the period of stress. Plasma corticosterone levels were significantly increased by both social defeat and witness trauma stress when compared to unstressed controls. Voiding analysis revealed a significant decrease in voiding frequency in the social defeat group compared to control animals, indicating an altered voiding phenotype. Witness trauma did not alter voiding behavior. Bladder contractile responses to cholinergic stimulation were not significantly altered in either stress group, nor was relaxation to the beta-adrenoceptor agonist isoprenaline. However, nerve evoked contractile responses were significantly increased at all frequencies in bladders from social defeat but not witness trauma mice. Purinergic contractile responses were also significantly enhanced in this group. Social defeat also resulted in increased urothelial acetylcholine release during bladder distension, with no change in ATP release. In conclusion, functional bladder changes are dependent upon stressor type. Enhanced urothelial acetylcholine may desensitize bladder sensory nerves, which, coupled with more efficient voiding contractions due to enhanced nerve-mediated and purinergic detrusor responses, may account for the altered voiding phenotype observed. This study reports a male model of social defeat stress with reduced urinary frequency, with no voiding changes observed in the witness.
心理应激与膀胱功能障碍有关,然而,受影响的膀胱局部机制尚不清楚。本研究旨在确定社会挫败或目睹创伤引起的心理应激如何影响排尿行为和膀胱功能。将雄性C57Bl/6J小鼠对与一只攻击性ARC(S)小鼠置于定制的有机玻璃箱中,每天1小时,共10天。社会挫败小鼠与攻击者有身体接触,而目睹者则在身体上隔开,但可以观察其笼伴与攻击者之间的互动。使用年龄匹配的对照小鼠对进行比较。在这10天内定期进行排尿分析。应激期结束后,使用整个膀胱标本评估功能变化。与未应激的对照组相比,社会挫败和目睹创伤应激均使血浆皮质酮水平显著升高。排尿分析显示,与对照动物相比,社会挫败组的排尿频率显著降低,表明排尿表型发生改变。目睹创伤并未改变排尿行为。两个应激组对胆碱能刺激的膀胱收缩反应均无显著改变,对β-肾上腺素能受体激动剂异丙肾上腺素的舒张反应也无显著改变。然而,社会挫败小鼠膀胱的神经诱发收缩反应在所有频率下均显著增加,而目睹创伤小鼠则没有。该组的嘌呤能收缩反应也显著增强。社会挫败还导致膀胱扩张期间尿路上皮乙酰胆碱释放增加,而ATP释放没有变化。总之,膀胱功能变化取决于应激源类型。尿路上皮乙酰胆碱的增加可能会使膀胱感觉神经脱敏,再加上神经介导和嘌呤能逼尿肌反应增强导致更有效的排尿收缩,这可能解释了观察到的排尿表型改变。本研究报告了一种社会挫败应激的雄性模型,其排尿频率降低,而目睹者未观察到排尿变化。