OSCR

Transcriptional Response to Chronic Long-Access Fentanyl Self-Administration in Rat Habenula and Amygdala.

Code ↔ Paper

12 matches between paragraphs of the paper and lines of its authors' code, computed by the harvester (lexical-v1). Click a colored paragraph or line to see its counterpart.

The 12 matches
  1. [1] § Materials and Methods Summary › Experiment Summary and RNA‐Seq Data Generation ↔ code/09_SRA/03_metadata.R, lines 1–55 · score 0.98 · inside sound attenuating, operant chambers housed, bilateral tissue punches, Ribosomal RNA depletion, Cayman Chemical, coronal slabs
  2. [2] § Results › Shared and Unique Gene Expression Changes in Hb and Amyg Following Chronic Fentanyl Intake ↔ code/06_GO_KEGG/01_GO_KEGG_Analyses.R, lines 548–592 · score 0.97 · gastric acid secretion, ECM receptor interaction, Parkinson disease, actin cytoskeleton, oxidative phosphorylation, glutamatergic synapse
  3. [3] § Results › Shared and Unique Gene Expression Changes in Hb and Amyg Following Chronic Fentanyl Intake ↔ code/05_DEA/01_Modeling.R, lines 477–532 · score 0.96 · Atp5mc2, Atp6v0e2, Atp6v1e1, Slc39a10, Col4a3, KEGG term
  4. [4] § Results › Shared and Unique Gene Expression Changes in Hb and Amyg Following Chronic Fentanyl Intake ↔ code/05_DEA/01_Modeling.R, lines 477–532 · score 0.91 · Cox6b1, Scn1a, Col9a3, Gria4, Grik1, Kcnj10
  5. [5] § Results › Shared and Unique Gene Expression Changes in Hb and Amyg Following Chronic Fentanyl Intake ↔ code/06_GO_KEGG/01_GO_KEGG_Analyses.R, lines 548–592 · score 0.87 · postsynaptic membrane potential, Col9a3, voltage gated, cation channels, Epha4, Gsn
  6. [6] § Materials and Methods Summary › Experiment Summary and RNA‐Seq Data Generation ↔ code/09_SRA/03_metadata.R, lines 1–55 · score 0.76 · bulk RNA sequencing, jugular catheters, house light, illumination, Drug, daily
  7. [7] § Materials and Methods Summary › Differential Gene Expression (DGE) ↔ code/06_GO_KEGG/01_GO_KEGG_Analyses.R, lines 73–188 · score 0.75 · enriched GO term, cellular components, Biological processes, molecular functions, enrichment, Amyg
  8. [8] § Results › Enrichment of Genes Associated With Fentanyl Intake in Human and Rodent Hb and Amyg Cell Types ↔ code/08_GSEA/01_enrich_DEGs_vs_cell_type_markers.R, lines 896–934 · score 0.65 · fine cell, DRD1, LAMP5, SATB2, nostrin, S14
  9. [9] § Results › Enrichment of Genes Associated With Fentanyl Intake in Human and Rodent Hb and Amyg Cell Types ↔ code/08_GSEA/01_enrich_DEGs_vs_cell_type_markers.R, lines 1295–1361 · score 0.63 · LHb.2, LHb.6, LHb.7, astrocytes, enriched, orthologous
  10. [10] § Materials and Methods Summary › Experiment Summary and RNA‐Seq Data Generation ↔ code/03_Data_preparation/01_build_objects.R, lines 47–85 · score 0.62 · tissue punches, library preparation, sequenced, RNA, brains, Amyg
  11. [11] § Materials and Methods Summary › RNA‐Seq Data Processing and Quality Control ↔ code/04_EDA/01_QCA.R, lines 2–87 · score 0.59 · quality control, expressed genes, QC metrics, RNA extraction, brain regions, filtered
  12. [12] § Materials and Methods Summary › Experiment Summary and RNA‐Seq Data Generation ↔ code/04_EDA/03_Explore_gene_level_effects.R, lines 2–55 · score 0.54 · linear regression, infusion slopes, mg, hour, RNA, intake

Paper

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The authors' code

R · 1,005 lines · 57 KB · MIT · 3 matches

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It can be read at the source: code/06_GO_KEGG/01_GO_KEGG_Analyses.R.

Overview

  1. Department of Psychological and Brain Sciences, Krieger School of Arts and Sciences, Johns Hopkins University, Baltimore, Maryland, USA
  2. Lieber Institute for Brain Development, Johns Hopkins Medical Campus, Baltimore, Maryland, USA
  3. Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA
  4. The Solomon H. Snyder Department of Neuroscience, Johns Hopkins School of Medicine, Baltimore, Maryland, USA
  5. Medical Scientist Training Program, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
  6. Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA
  7. Kavli Neuroscience Discovery Institute, Johns Hopkins University, Baltimore, Maryland, USA
  8. Center for Computational Biology, Johns Hopkins University, Baltimore, Maryland, USA
Institutions: Johns Hopkins University (United States); Lieber Institute for Brain Development (United States); Johns Hopkins Medicine (United States)
Journal: Addiction biology, volume 31, issue 7, article e70179
Dates: received 25 January 2026; accepted 24 June 2026; published online 14 July 2026; in print July 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1111/adb.70179 · PMID 42444546 · PMCID PMC13366401 · OpenAlex W4417361577
Open access: gold, a free copy (OpenAlex)
Status: code verified
Categories: genetics / omics (modality), human (organism), rat (organism), other condition (population), pain (population), cellular / molecular (subfield)
Methods: Statistics, Smoothing, state filtering, decompositions
MeSH: Amygdala*, Analgesics, Opioid*, Fentanyl*, Habenula*, Transcriptome*, Animals, Gene Expression Profiling, Male, Rats, Rats, Sprague-Dawley, Self Administration (* major topic)
Topic: Neurogenesis and neuroplasticity mechanisms (Developmental Neuroscience, Neuroscience), according to OpenAlex
Funding: NIDA NIH HHS (R01 DA035943, R21 DA060407); NIH HHS (R01DA035943, T32MH015330, R21DA060407); National Institutes of Health (T32MH015330, R01DA035943, R21DA060407); NIMH NIH HHS (T32 MH015330); Lieber Institute for Brain Development
Citations: cited by 1 paper (Europe PMC); 104 references in the paper

Abstract

Fentanyl is a potent synthetic opioid associated with overdose. However, little is known about fentanyl‐induced molecular adaptations in the habenula and amygdala, two brain regions implicated in opioid use and withdrawal. We performed bulk RNA‐sequencing in the rat habenula and amygdala to identify transcriptomic changes associated with fentanyl intake. Male rats self‐administered intravenous saline or fentanyl over 22–24 days. Ninety minutes following the final session, brains were collected for transcriptomic profiling. In Hb, we identified 453 differentially expressed genes (DEGs) between saline and fentanyl rats, with upregulated genes associated with synaptic transmission and ionic conductance. In the amygdala, we identified 3041 fentanyl‐associated DEGs with upregulated genes implicated in metabolic and vesicular functions. Downregulated genes in both regions were enriched for extracellular matrix functions. Integration of DEGs with single‐cell RNA‐sequencing data from rodents and humans revealed that fentanyl DEGs were enriched in specific habenula and amygdala cell type markers. Furthermore, fentanyl downregulated DEGs in the amygdala were enriched in genes associated with the risk for substance use disorders. Together, we define how fentanyl intake alters transcriptional programs in the rat habenula and amygdala, and we link these changes to specific human cell types and risk genes for neuropsychiatric disorders and addiction.

Reproduced under the paper's license (CC BY), from the paper cited above.

Repositories

Its files are read in the Code ↔ Paper reader above, with 12 matches between paragraphs and lines of code.

LieberInstitute/fentanyl_rat_hb_amy

License: MIT
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: 4284ebac39e53fe23aea2a23812dc71441c14e10, 15 July 2026
Languages: R (17), Shell (9)
Size: 489 files, 26 scripts
Software Heritage: not archived
Found in: “Data Availability Statement”
Holds: README
Not found: license file, CITATION.cff, environment file, tests, continuous integration, documentation
Tools: cowplot (9 files), ggplot2 (9 files), tidyverse (9 files), ComplexHeatmap (3 files), edgeR (2 files), pheatmap (2 files), circlize (1 file), clusterProfiler (1 file), data.table (1 file), limma (1 file), lme4 (1 file), Nextflow (1 file), reshape2 (1 file), rstatix (1 file), Seurat (1 file), SingleCellExperiment (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
27 files, not copied: shown from their source

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Zenodo 17573970

License: CC-BY-4.0
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Size: 1 file
Software Heritage: not checked
Found in: the references
Not found: README, license file, CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 27 September 2026: the link answers (HTTP 200)
  • 27 September 2026: the link answers (HTTP 200)
At the source:

The paper's code and data availability statement is in the Data section.

Tracing map

Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.

What the map holds:

  • 2 repositories of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 26 scripts, each with its path and the digest of its content;
  • 12 matches between paragraphs of the paper and lines of the code (method lexical-v1);
  • neither the text of the paper nor the code itself.

Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.

Data

No dataset and no data link were found in the paper.

Data Availability Statement

The source FASTQ files are publicly available from the NCBI Sequence Read Archive BioProject PRJNA1179901. All analysis code is available at https://github.com/LieberInstitute/fentanyl_rat_hb_amy [104].

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 2, 28 September 2026

  • Authors: added Ege A Yalcinbas (0000-0002-9480-7192); Emma Chaloux‐Pinette (0000-0002-6832-6862); Nicholas J Eagles (0000-0002-9808-5254); Michael S Totty (0000-0002-9292-8556); Patricia H Janak (0000-0002-3333-9049); Kristen R Maynard (0000-0003-0031-8468); removed Ege A Yalcinbas; Emma Chaloux‐Pinette; Nicholas J Eagles; Michael S Totty; Patricia H Janak; Kristen R Maynard

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 9 authors, 11 MeSH terms, 5 funders, 103 references.

Cite

This paper

Magnard, R., Gonzalez‐Padilla, D., Yalcinbas, E. A., Chaloux‐Pinette, E., Eagles, N. J., Totty, M. S., Janak, P. H., Collado‐Torres, L., & Maynard, K. R. (2026). Transcriptional Response to Chronic Long-Access Fentanyl Self-Administration in Rat Habenula and Amygdala. Addiction biology, 31(7), e70179. https://doi.org/10.1111/adb.70179

BibTeX

@article{magnard2026transcriptional,
author = {Magnard, Robin and Gonzalez‐Padilla, Daianna and Yalcinbas, Ege A and Chaloux‐Pinette, Emma and Eagles, Nicholas J and Totty, Michael S and Janak, Patricia H and Collado‐Torres, Leonardo and Maynard, Kristen R},
title = {{Transcriptional Response to Chronic Long-Access Fentanyl Self-Administration in Rat Habenula and Amygdala}},
journal = {Addiction biology},
year = {2026},
month = jul,
volume = {31},
number = {7},
pages = {e70179},
publisher = {Wiley},
issn = {1355-6215},
doi = {10.1111/adb.70179},
url = {https://doi.org/10.1111/adb.70179},
pmid = {42444546},
pmcid = {PMC13366401}
}

RIS

TY - JOUR
AU - Magnard, Robin
AU - Gonzalez‐Padilla, Daianna
AU - Yalcinbas, Ege A
AU - Chaloux‐Pinette, Emma
AU - Eagles, Nicholas J
AU - Totty, Michael S
AU - Janak, Patricia H
AU - Collado‐Torres, Leonardo
AU - Maynard, Kristen R
TI - Transcriptional Response to Chronic Long-Access Fentanyl Self-Administration in Rat Habenula and Amygdala
T2 - Addiction biology
J2 - Addict Biol
PY - 2026
DA - 2026/07/01
VL - 31
IS - 7
SP - e70179
SN - 1355-6215
PB - Wiley
DO - 10.1111/adb.70179
UR - https://doi.org/10.1111/adb.70179
LA - en
ER -

CSL-JSON

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