Evidence map›Paper›PMID 40320991›Full record

ArticleBrain and behavior2025

Nicotinamide Adenine Dinucleotide Supplementation Improves Cuprizone-Induced Multiple Sclerosis-Related Behavioral Changes in C57BL/6J Mice.

Shuang Song, Ruoyi Guo, Jiangyuan Guo, Bin Li, Yusen Han, Huining Zhang, Li Guo

Abstract read
In one paragraph

Article in Brain and behavior, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shuang SongDepartment of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Ruoyi GuoDepartment of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.ORCID https://orcid.org/0000-0002-7901-8427
Jiangyuan GuoDepartment of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Bin LiDepartment of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Yusen HanDepartment of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Huining ZhangDepartment of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Li GuoDepartment of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

Funding

Hebei Natural Science Foundation H2023206107Medical Science Research Project of Hebei 20241859
6 · The paper itself

Abstract

objectiveTo investigate whether nicotinamide adenine dinucleotide (NAD+) supplementation can improve behavioral changes in a cuprizone-intoxicated mouse model.

methodsSix-week-old C57BL/6J mice were divided into three groups: two were fed 0.2% cuprizone chow (cuprizone and cuprizone + NAD+ groups), and the other group was fed normal rodent chow (control group) for 4 weeks. The mice in the cuprizone + NAD+ group received 250 mg/kg/day NAD+ intraperitoneally once a day, while the other mice were administered saline simultaneously. Behavioral tests for spatial memory (Morris water maze and Y maze), locomotor ability (grip test and rotarod test), depression-like behavior (open field test and tail suspension test), and exploratory behavior (open field test) were conducted.

resultsIn the probe test of the Morris water maze, the cuprizone group spent a significantly smaller proportion of time in the target quadrant than the control group did (16.32% vs. 31.66%, p = 0.006). However, supplementation with NAD+ increased the value (28.78% vs. 16.32%, p = 0.023). Similarly, in the Y maze test, the cuprizone group demonstrated a notably lower ratio of effective alterations compared to the control group (0.543 vs. 0.648, p < 0.001), and the cuprizone + NAD+ group presented an improved ratio compared with the cuprizone group (0.613 vs. 0.543, p = 0.021). Compared with the control group, cuprizone toxicity resulted in a decreased time to fall (169.10 vs. 247.60 s, p = 0.015) in the grip test, but NAD+ supplementation mitigated this effect (261.60 vs. 169.10 s, p = 0.003). There were no significant differences in the immobile time among groups in both the tail suspension test and the open field test, and there were also no significant differences in center distance in the open field test.

conclusionsDirect NAD+ supplementation improves the locomotor ability and spatial memory of cuprizone-intoxicated C57BL/6J mice. However, NAD+ supplementation does not show significant effects on depressive and exploratory behavior of experimental mice.

Indexed as

Behavior, AnimalMultiple SclerosisNADAnimalsCuprizoneDepressionDietary SupplementsDisease Models, AnimalExploratory BehaviorMaleMaze LearningMiceMice, Inbred C57BLSpatial MemoryCuprizoneNADbehavioral changescuprizonenicotinamide adenine dinucleotide

Identifiers

PMID40320991
PMCPMC12050637

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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.