Evidence map›Paper›PMID 38977070›Full record

ArticleNeuroscience2024

Subregion-specific transcriptomic profiling of rat brain reveals sex-distinct gene expression impacted by adolescent stress.

Kristen N Krolick, Jingyi Cao, Evelyn M Gulla, Meeta Bhardwaj, Samantha J Marshall, Ethan Y Zhou, Andor J Kiss, Fouad Choueiry, Jiangjiang Zhu, Haifei Shi

Abstract read
In one paragraph

Article in Neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

10 authors.

Kristen N KrolickDepartment of Biology, Miami University, Oxford, OH 45056, USA. Electronic address: krolickn@miamioh.edu.
Jingyi CaoDepartment of Biology, Miami University, Oxford, OH 45056, USA. Electronic address: caoj2@miamioh.edu.
Evelyn M GullaDepartment of Biology, Miami University, Oxford, OH 45056, USA. Electronic address: gullaem@miamioh.edu.
Meeta BhardwajDepartment of Biology, Miami University, Oxford, OH 45056, USA. Electronic address: meetabhardwaj@miamioh.edu.
Samantha J MarshallDepartment of Biology, Miami University, Oxford, OH 45056, USA. Electronic address: zhouey@miamioh.edu.
Ethan Y ZhouDepartment of Biology, Miami University, Oxford, OH 45056, USA. Electronic address: zhouey@miamioh.edu.
Andor J KissCenter for Bioinformatics & Functional Genomics, Miami University, Oxford, OH 45056, USA. Electronic address: kissaj@miamioh.edu.
Fouad ChoueiryDepartment of Human Sciences, The Ohio State University, Columbus, OH 43210, USA. Electronic address: choueiry.2@byckeyemail.osu.edu.
Jiangjiang ZhuDepartment of Human Sciences, The Ohio State University, Columbus, OH 43210, USA; James Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA. Electronic address: zhu.2484@osu.edu.
Haifei ShiDepartment of Biology, Miami University, Oxford, OH 45056, USA. Electronic address: shih@miamioh.edu.

Funding

Characterizing the Metabolome and Volatilome of Gut MicrobiomeR35GM133510 · NIGMS · OHIO STATE UNIVERSITY · PI ZHU, JIANGJIANG · 2019 to 2023
$2.2M
Central Action of Brain-Derived Neurotrophic Factor in Male and Female RatsR15DK090823 · NIDDK · MIAMI UNIVERSITY OXFORD · PI SHI, HAIFEI · 2010 to 2015
$816k
NIDDK NIH HHS R15 DK090823NIGMS NIH HHS R35 GM133510
6 · The paper itself

Abstract

Stress during adolescence clearly impacts brain development and function. Sex differences in adolescent stress-induced or exacerbated emotional and metabolic vulnerabilities could be due to sex-distinct gene expression in hypothalamic, limbic, and prefrontal brain regions. However, adolescent stress-induced whole-genome expression changes in key subregions of these brain regions were unclear. In this study, female and male adolescent Sprague Dawley rats received one-hour restraint stress daily from postnatal day (PD) 32 to PD44. Corticosterone levels, body weights, food intake, body composition, and circulating adiposity and sex hormones were measured. On PD44, brain and blood samples were collected. Using RNA-sequencing, sex-specific differences in stress-induced differentially expressed (DE) genes were identified in subregions of the hypothalamus, limbic system, and prefrontal cortex. Canonical pathways reflected well-known sex-distinct maladies and diseases, substantiating the therapeutic potential of the DE genes found in the current study. Thus, we proposed specific sex distinct, adolescent stress-induced transcriptional changes found in the current study as examples of the molecular bases for sex differences witnessed in stress induced or exacerbated emotional and metabolic disorders. Future behavioral studies and single-cell studies are warranted to test the implications of the DE genes identified in this study in sex-distinct stress-induced susceptibilities.

Indexed as

BrainGene Expression ProfilingRats, Sprague-DawleySex CharacteristicsStress, PsychologicalAnimalsCorticosteroneFemaleMalePrefrontal CortexRatsTranscriptomeCorticosteroneAmygdalaChronic restraint stressHippocampusHypothalamusOrbitofrontal cortexSex-specific differences

Identifiers

PMID38977070
PMCPMC11444371

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.