Evidence map›Paper›PMID 39921359›Full record

ArticleNeuropsychopharmacology reports2025

Gene Expression Profiling in the Cortex of Fabp4 Knockout Mice.

Hinako Kirikae, Xiaofeng He, Tetsuo Ohnishi, Hirofumi Miyazaki, Takeo Yoshikawa, Yuji Owada, Motoko Maekawa

Abstract read
In one paragraph

Article in Neuropsychopharmacology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Hinako KirikaeDepartment of Organ Anatomy, Tohoku University Graduate School of Medicine, Sendai, Japan.
Xiaofeng HeDepartment of Organ Anatomy, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tetsuo OhnishiDepartment of Nutrition, Akita Nutrition Junior College, Akita, Japan.
Hirofumi MiyazakiDepartment of Organ Anatomy, Tohoku University Graduate School of Medicine, Sendai, Japan.
Takeo YoshikawaLaboratory for Molecular Psychiatry, RIKEN Center for Brain Science Wako, Saitama, Japan.
Yuji OwadaDepartment of Organ Anatomy, Tohoku University Graduate School of Medicine, Sendai, Japan.
Motoko MaekawaDepartment of Organ Anatomy, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID https://orcid.org/0000-0002-0816-5550

Funding

Food Science Institute Foundation 2023A10Foundation for Dietary Scientific ResearchJapan Society for the Promotion of Science JP22K19502Japan Society for the Promotion of Science JP23K24252Japan Society for the Promotion of Science JP23K24783Japan Society for the Promotion of Science JP24KJ0388JST Program for Co-Creating Startup Ecosystem JPMJSF2312KOSÉ Cosmetology Research FoundationMishima Kaiun Memorial FoundationSENSHIN Medical Research FoundationShiseido Female Researcher Science GrantSumitomo FoundationTohoku UniversityTojuro Iijima Foundation for Food Science and Technology
6 · The paper itself

Abstract

aimsFatty acid binding protein 4, adipocyte (Fabp4), is well known for its role in peripheral lipid metabolism, but its potential role in brain function remains largely unexplored. This study aimed to investigate Fabp4 expression in the adult mouse brain and explore gene expression changes in Fabp4 knockout (KO) mice to assess its potential impact on brain function.

methodsWe conducted in situ hybridization to assess Fabp4 expression in key brain regions of adult mice. In parallel, differential gene expression analysis using RNA-seq was conducted in the prefrontal cortex of Fabp4 KO mice to identify genes affected by Fabp4 deficiency.

resultsNo Fabp4 expression was detected in the brains of mice, suggesting a lack of direct involvement in the central nervous system. However, Fabp4 KO mice exhibited significant changes in gene expression in the brain, with 31 genes upregulated and 30 downregulated. Downregulated genes were linked to histone methylation and metabolic processes, while upregulated ones were associated with synaptic organization.

conclusionAlthough Fabp4 is not expressed in the brain, its deficiency leads to substantial changes in gene expression, likely mediated by peripheral metabolic pathways and epigenetic regulation. These changes may explain the previously observed autism-like behaviors and increased dendritic spine density in Fabp4 KO mice. This study sheds light on the role of systemic lipid metabolism in neurodevelopmental disorders such as autism spectrum disorder (ASD) and highlights epigenetic mechanisms as potential mediators of these effects.

Indexed as

Fatty Acid-Binding ProteinsPrefrontal CortexAnimalsGene Expression ProfilingMaleMiceMice, Inbred C57BLMice, KnockoutFabp4 protein, mouseFatty Acid-Binding Proteinsautism spectrum disorderepigenetic gene expressionFabp4 knockout (KO) miceRNA‐seqsynaptic gene expression

Identifiers

PMID39921359
PMCPMC11806211

What Socratic holds

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Registered trials

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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 Socratic graph.