Evidence map›Paper›PMID 31391260›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

Change in Brain Plasmalogen Composition by Exposure to Prenatal Undernutrition Leads to Behavioral Impairment of Rats.

Kodai Hino, Shunya Kaneko, Toshiya Harasawa, Tomoko Kimura, Shiro Takei, Masakazu Shinohara, Fumiyoshi Yamazaki, Shin-Ya Morita, Shumpei Sato, Yoshihito Kubo and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Pharmaceutics · 2026
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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

18 authors at 5 institutions in 2 countries.

Kodai HinoDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan.
Shunya KanekoDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan.
Toshiya HarasawaDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan.
Tomoko KimuraDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan.
Shiro TakeiDepartment of Environmental Biology, College of Bioscience and Biotechnology, Chubu University, Kasugai 487-8501, Japan.
Masakazu ShinoharaDivision of Epidemiology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.
Fumiyoshi YamazakiInternational Mass Imaging Center and Department of Cellular and Molecular Anatomy, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Shin-Ya MoritaDepartment of Pharmacy, Shiga University of Medical Science Hospital, Shiga 520-2192, Japan.ORCID 0000-0003-4079-707X
Shumpei SatoInternational Mass Imaging Center and Department of Cellular and Molecular Anatomy, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.
Yoshihito KuboDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan.
Tadaaki KonoDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan.
Mitsutoshi SetouInternational Mass Imaging Center and Department of Cellular and Molecular Anatomy, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan.ORCID 0000-0002-1302-6467
Mina YoshiokaDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan.
Junya FujinoDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan.ORCID 0000-0002-5285-2032
Hiroyuki SugiharaDivision of Molecular Diagnostic Pathology, Department of Pathology, Shiga University of Medical Science, Otsu 520-2192, Japan.
Hideto KojimaDepartment of Stem Cell Biology and Regenerative Medicine, Shiga University of Medical Science, Otsu 520-2192, Japan, and.
Naoto YamadaDepartment of Psychiatry, Shiga University of Medical Science, Otsu 520-2192, Japan.
Jun UdagawaDivision of Anatomy and Cell Biology, Department of Anatomy, Shiga University of Medical Science, Otsu 520-2192, Japan, udagawa@belle.shiga-med.ac.jp.ORCID 0000-0002-6573-9434
Shiga University of Medical Science · JPHamamatsu University School of Medicine · JPChubu University · JPKobe University · JPShiga University of Medical Science Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidemiological studies suggest that poor nutrition during pregnancy influences offspring predisposition to experience developmental and psychiatric disorders. Animal studies have shown that maternal undernutrition leads to behavioral impairment, which is linked to alterations in monoaminergic systems and inflammation in the brain. In this study, we focused on the ethanolamine plasmalogen of the brain as a possible contributor to behavioral disturbances observed in offspring exposed to maternal undernutrition. Maternal food or protein restriction between gestational day (GD) 5.5 and GD 10.5 resulted in hyperactivity of rat male adult offspring. Genes related to the phospholipid biosynthesis were found to be activated in the PFC, but not in the NAcc or striatum, in the offspring exposed to prenatal undernutrition. Corresponding to these gene activations, increased ethanolamine plasmalogen (18:0p-22:6) was observed in the PFC using mass spectrometry imaging. A high number of crossings and the long time spent in the center area were observed in the offspring exposed to prenatal undernutrition and were mimicked in adult rats via the intravenous injection of ethanolamine plasmalogen (18:0p-22:6) incorporated into the liposome. Additionally, plasmalogen (18:0p-22:6) increased only in the PFC, and not in the NAcc or striatum. These results suggest that brain plasmalogen is one of the key molecules to control behavior, and its injection using liposome is a potential therapeutic approach for cognitive impairment.

Indexed as

AnimalsBehavior, AnimalFemaleMaleMalnutritionPlasmalogensPrefrontal CortexPregnancyPrenatal Exposure Delayed EffectsRatsRats, Wistarphosphatidal ethanolaminesPlasmalogenshyperactivitymaternal undernutritionplasmalogen phosphatidylethanolamineprefrontal cortex

Identifiers

PMID31391260
PMCPMC6764206
OpenAlexW2965136698

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.