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在C57BL/6J小鼠中,多巴胺受体1激动剂SKF-38393的消耗以性别特异性方式降低了持续光照诱导的多动、抑郁样和焦虑样行为。

Consumption of dopamine receptor 1 agonist SKF-38393 reduces constant-light-induced hyperactivity, depression-like, and anxiety-like behaviors in a sex specific manner in C57BL/6J mice.

作者信息

Guindon Grace E, Anzalone Alexis, Burke Samantha G, Murphy Cloey A, Milano Maria E, Price John C, Tadros Stephanie, McFarland Alexander T, Contini Fernanda Medieros, Seggio Joseph A

机构信息

Department of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.

出版信息

Front Behav Neurosci. 2025 Mar 12;19:1537048. doi: 10.3389/fnbeh.2025.1537048. eCollection 2025.

DOI:10.3389/fnbeh.2025.1537048
PMID:40144749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11936926/
Abstract

Artificial light exposure during nighttime, including constant light (LL), is an increasingly prevalent environmental occurrence linked to impaired mood and cognitive impairments in both humans and animal models. Dopamine and dopamine 1 receptors are well known to modulate circadian rhythms and mood. This study investigated the effects of LL on anxiety-like, depressive-like, and cognitive behaviors in male and female C57BL/6J mice and assessed whether consumption of SKF-38393, a dopamine 1 receptor agonist, can mitigate these negative behavioral outcomes. Mice were exposed to LL or a standard 12:12 light:dark cycle (LD) for 6 weeks, with subgroups receiving either SKF-38393 or water. All mice had their circadian rhythms continuously monitored and were placed within behavioral tests that assayed their anxiety-like, depressive-like, and learning and memory behaviors. Behavioral assays revealed that LL increased hyperactivity and anxiety-like behaviors, which were mitigated by SKF-38393 consumption in both sexes. In addition, male mice exhibited anhedonia under LL, which was alleviated by SKF-38393, whereas female mice were resistant to LL-induced anhedonia. Sex differences emerged in fluid consumption independent of lighting condition, with females consuming more SKF-38393, and in responses to DA on behavior, including novel object recognition and exploration. These results indicate that low dose oral consumption of dopamine 1 receptor agonists can ameliorate some of the negative behavioral effects of LL exposure. This study highlights the complex interplay between chronic light, dopamine, and sex in influencing mood and behavior, suggesting potential modulatory roles for dopamine 1 receptor agonists in regulating behavioral outcomes to circadian disturbances.

摘要

夜间的人工光照暴露,包括持续光照(LL),是一种日益普遍的环境现象,与人类和动物模型中的情绪障碍和认知障碍有关。众所周知,多巴胺和多巴胺1受体可调节昼夜节律和情绪。本研究调查了持续光照对雄性和雌性C57BL/6J小鼠的焦虑样、抑郁样和认知行为的影响,并评估了多巴胺1受体激动剂SKF-38393的摄入是否可以减轻这些负面行为结果。将小鼠暴露于持续光照或标准的12:12光照:黑暗周期(LD)下6周,亚组分别给予SKF-38393或水。持续监测所有小鼠的昼夜节律,并将它们置于行为测试中,以检测它们的焦虑样、抑郁样以及学习和记忆行为。行为分析表明,持续光照增加了多动和焦虑样行为,两性摄入SKF-38393均可减轻这些行为。此外,雄性小鼠在持续光照下表现出快感缺失,SKF-38393可缓解这一症状,而雌性小鼠对持续光照诱导的快感缺失具有抗性。在液体消耗方面出现了与光照条件无关的性别差异,雌性消耗更多的SKF-38393,并且在对行为的多巴胺反应方面也存在性别差异,包括对新物体的识别和探索。这些结果表明,低剂量口服多巴胺1受体激动剂可以改善持续光照暴露的一些负面行为影响。本研究强调了慢性光照、多巴胺和性别在影响情绪和行为方面的复杂相互作用,表明多巴胺1受体激动剂在调节昼夜节律紊乱的行为结果方面具有潜在的调节作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/16c829e892fc/fnbeh-19-1537048-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/8abf11819e42/fnbeh-19-1537048-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/555389af32f5/fnbeh-19-1537048-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/2c75b7027ab7/fnbeh-19-1537048-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/16c829e892fc/fnbeh-19-1537048-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/8abf11819e42/fnbeh-19-1537048-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/555389af32f5/fnbeh-19-1537048-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/2c75b7027ab7/fnbeh-19-1537048-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f0/11936926/16c829e892fc/fnbeh-19-1537048-g004.jpg

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本文引用的文献

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Lights at night mediate depression-like behavioral and molecular phenotypes in a glucocorticoid-dependent manner in male rats.夜间灯光以糖皮质激素依赖的方式介导雄性大鼠的抑郁样行为和分子表型。
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