发育性多氯联苯暴露对排尿生理的影响持续到成年期,并影响小鼠对膀胱刺激的敏感性

IF 2.9 Q2 TOXICOLOGY
Monica Ridlon, Audrey Spiegelhoff, Conner L Kennedy, Thomas Lavery, Kathy Wang, Julia Tlapa, Tamryn Jordan, Lindsey Felth Tanaka, Kimberly Keil Stietz
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引用次数: 0

摘要

多氯联苯(PCBs)是存在于环境、食品、动物和人体组织中的有毒物质。多氯联苯与许多不利的健康影响有关;然而,多氯联苯暴露对下尿路功能的影响是一个相对较新的研究领域。我们之前发现,小鼠在发育过程中(在子宫和哺乳期)暴露于与人类相关的多氯联苯混合物会导致6周龄时排尿生理的性别和剂量依赖性变化。本研究扩展了先前的研究结果,以调查发育多氯联苯诱导的排尿表型是否在小鼠年龄到12周龄时持续或改变。通过空斑试验、尿流测定和膀胱测定法进行的排尿生理测试表明,在12周龄时,多氯联苯暴露有几种性别和剂量依赖性影响。此外,与先前研究中的年轻成年小鼠相比,功能障碍模式要么保持不变,要么新获得,要么逆转。在这里,发育过程中接触多氯联苯以剂量依赖的方式减少了成年雄性和雌性小鼠的小尿点数量,并且通过麻醉膀胱术评估,雌性小鼠有更频繁的排尿事件。当膀胱内灌注辣椒素以瞬时受体电位阳离子通道亚家族V成员1 (TRPV1)介导的途径为靶点时,小鼠也出现了PCB剂量依赖性的排尿生理变化。多氯联苯阻断或加剧辣椒素诱导的反应取决于所检查的终点,这表明该途径可能在多氯联苯依赖性排尿变化中发挥作用。多氯联苯对前列腺湿重也有微妙的影响,与低剂量的多氯联苯相比,高剂量的多氯联苯会减少组织质量,而与对照组没有差异。本研究表明,在体内平衡条件下和辣椒素挑战下,多氯联苯的发育暴露在成年期至少12周龄的下尿路功能继续受到影响。更好地了解多氯联苯等早期生活压力因素如何导致与年龄相关的排尿功能障碍是必要的,因为这些发现可能有助于降低风险或改善患有下尿路症状的患者的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Developmental polychlorinated biphenyl (PCB) exposure impacts on voiding physiology persist into adulthood and influence sensitivity to bladder stimuli in mice

Developmental polychlorinated biphenyl (PCB) exposure impacts on voiding physiology persist into adulthood and influence sensitivity to bladder stimuli in mice
Polychlorinated biphenyls (PCBs) are toxicants present in the environment, foodstuff, animal and human tissues. PCBs are linked to numerous adverse health effects; however, impacts of developmental PCB exposure on lower urinary tract function are a comparatively newer area of interest. We have previously found developmental exposure (in utero and lactational) to a human-relevant PCB mixture in mice leads to sex- and dose- dependent changes to urinary voiding physiology at 6 weeks of age. This study expands upon previous findings to investigate if developmental PCB-induced urinary voiding phenotypes persist or shift as mice age to 12 weeks of age. Urinary voiding physiology testing through void spot assays, uroflowmetry, and cystometry demonstrated several sex- and dose- dependent effects of PCB exposure at 12 weeks of age. Further, patterns of dysfunction were either maintained, newly acquired, or reversed compared to those from younger adult mice in a previous study. Here, developmental PCB exposure decreased number of small urine spots in adult male and female mice in a dose dependent manner, and female mice had more frequent voiding events assessed by anesthetized cystometry. Mice also had PCB dose-dependent changes to urinary voiding physiology when challenged with intravesical capsaicin infusion to target transient receptor potential cation channel subfamily V member 1 (TRPV1)-mediated pathways. PCBs either blocked or exacerbated capsaicin induced responses depending on the endpoint examined, suggesting this pathway may play a role in PCB-dependent changes in voiding. PCBs also had subtle impacts on prostate wet weight, with high PCB doses reducing tissue mass compared to low PCB doses, while none differed from vehicle. This study demonstrates developmental exposure to PCBs continues to impact lower urinary tract function in adulthood to at least 12 weeks of age both during homeostatic conditions and upon challenge of capsaicin. Better understanding of how early life stressors like PCBs contribute to aging-associated voiding dysfunction are imperative as these findings may help mitigate risk or improve treatment strategies for patients suffering from lower urinary tract symptoms.
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来源期刊
Current Research in Toxicology
Current Research in Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
4.70
自引率
3.00%
发文量
33
审稿时长
82 days
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