Evidence map›Paper›PMID 41019781›Full record

ArticleFrontiers in molecular neuroscience2025

Divergent and subnucleus-specific gene expression responses to chronic stress hormone exposure in the amygdala.

Shuhei Ueda, Manami Kakita, Masahito Hosokawa, Koji Arikawa, Kiyofumi Takahashi, Ryusuke Shiota, Masaki Kakeyama, Hiroko Matsunaga, Haruko Takeyama, Sayaka Takemoto-Kimura

Abstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 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

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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

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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. 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.

Shuhei UedaDepartment of Neuroscience, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.
Manami KakitaDepartment of Neuroscience, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.
Masahito HosokawaGraduate School of Advanced Science and Engineering, Waseda University, Tokyo, Japan.
Koji ArikawaResearch Organization for Nano and Life Innovation, Waseda University, Tokyo, Japan.
Kiyofumi TakahashiResearch Organization for Nano and Life Innovation, Waseda University, Tokyo, Japan.
Ryusuke ShiotaDepartment of Neuroscience, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.
Masaki KakeyamaLaboratory for Systems Neurosciences and Preventive Medicine, Faculty of Human Sciences, Waseda University, Tokorozawa, Japan.
Hiroko MatsunagaResearch Organization for Nano and Life Innovation, Waseda University, Tokyo, Japan.
Haruko TakeyamaGraduate School of Advanced Science and Engineering, Waseda University, Tokyo, Japan.
Sayaka Takemoto-KimuraDepartment of Neuroscience, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major depressive disorder (MDD) is one of the most prevalent mental disorders, posing a significant socioeconomic burden worldwide. Its development involves both genetic and environmental factors, among which chronic stress is considered a major contributor. The amygdala, a key brain region for emotional regulation, is critically implicated in MDD pathophysiology. Given its complex subnuclear architecture, it is essential to characterize stress-induced molecular changes at the level of individual subnuclei. To investigate subnucleus-specific molecular adaptations to chronic stress, we performed RNA sequencing on fluorescence-guided micropunch samples from five amygdala-related subnuclei in mice exposed to chronic corticosterone (CORT): the basolateral amygdala (BLA), the lateral and medial central amygdala (CeL, CeM), and the oval and fusiform bed nuclei of the stria terminalis (BNSTov, BNSTfu). Comparative transcriptomic analysis revealed highly divergent and subnucleus-resolved gene expression responses to chronic CORT exposure. Each subregion exhibited unique profiles of differentially expressed genes, implicating alterations in excitatory-inhibitory synaptic balance, glial functions involving oligodendrocytes or astrocytes, and neuropeptide signaling. Our results uncover the molecular heterogeneity of subnucleus-specific responses within the amygdala. These findings highlight the importance of anatomically resolved analyses in elucidating the biological basis of stress-related mental disorders such as MDD, thereby paving the way for more targeted therapeutic strategies.

Indexed as

amygdalacentral extended amygdalacorticosteronedepressionHPA axisRNA-seqstress

Identifiers

PMID41019781
PMCPMC12463952

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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.