Evidence map›Paper›PMID 40144749›Full record

ArticleFrontiers in behavioral neuroscience2025

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.

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

Abstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Grace E GuindonDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
Alexis AnzaloneDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
Samantha G BurkeDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
Cloey A MurphyDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
Maria E MilanoDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
John C PriceDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
Stephanie TadrosDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
Alexander T McFarlandDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
Fernanda Medieros ContiniDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.
Joseph A SeggioDepartment of Biological Sciences, Bridgewater State University, Bridgewater, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

anhedoniacircadian rhythmdopaminelightmouse behavioropen field (OF)

Identifiers

PMID40144749
PMCPMC11936926

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.