Evidence map›Paper›PMID 33848264›Full record

ArticleThe Journal of clinical investigation2021

The 5α-reductase inhibitor finasteride reduces opioid self-administration in animal models of opioid use disorder.

Gabriel D Bosse, Roberto Cadeddu, Gabriele Floris, Ryan D Farero, Eva Vigato, Suhjung J Lee, Tejia Zhang, Nilesh W Gaikwad, Kristen A Keefe, Paul Em Phillips and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. New directions in neurosteroid therapeutics in neuropsychiatry.Neuroscience and biobehavioral reviews · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

12 authors at 2 institutions in 1 country.

Gabriel D BosseDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Roberto CadedduDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Gabriele FlorisDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Ryan D FareroDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.
Eva VigatoDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Suhjung J LeeDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.
Tejia ZhangDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Nilesh W GaikwadGaikwad Steroidomics Laboratory, Davis, California, USA.
Kristen A KeefeDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Paul Em PhillipsDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA.
Marco BortolatoDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
Randall T PetersonDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, Utah, USA.
University of Utah · USUniversity of Washington · US

Funding

Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
MULTIDISCIPLINARY RESEARCH TRAINING IN CARDIOLOGYT32HL007208 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Patrick Thomas Ellinor, David E Sosnovik · 1985 to 2026
$16.1M
TRAINING IN THE MOLECULAR PHARMACOLOGY OF ABUSED DRUGST32DA007278 · NIDA · UNIVERSITY OF WASHINGTON · PI Susan Marie Ferguson, Paul E. M. Phillips · 1993 to 2026
$9.8M
Training Program in Genomic MedicineT32HG008962 · NHGRI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Lynn Jorde, Aaron R Quinlan · 2016 to 2026
$3.0M
Neural mechanisms regulating cocaine consumptionR37DA051686 · NIDA · UNIVERSITY OF WASHINGTON · PI PHILLIPS, PAUL E. M. · 2020 to 2024
$2.5M
Diametric changes in phasic dopamine to contingent and non-contingent drug cues in the regulation of drug taking and drug seekingR01DA039687 · NIDA · UNIVERSITY OF WASHINGTON · PI PHILLIPS, PAUL E. M. · 2015 to 2019
$1.7M
Expansion of a Zebrafish Research Core FacilityG20OD018369 · OD · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J. · 2014 to 2014
$500k
Exploring steroid-based therapies to reduce opioid abuseR21DA049530 · NIDA · UNIVERSITY OF UTAH · PI BORTOLATO, MARCO, PETERSON, RANDALL T · 2020 to 2021
$419k
CIHRNCATS NIH HHS UL1 TR002538NHGRI NIH HHS T32 HG008962NHLBI NIH HHS T32 HL007208NIDA NIH HHS R01 DA039687NIDA NIH HHS R21 DA049530NIDA NIH HHS R37 DA051686NIDA NIH HHS T32 DA007278NIH HHS G20 OD018369
6 · The paper itself

Abstract

Opioid use disorder (OUD) has become a leading cause of death in the United States, yet current therapeutic strategies remain highly inadequate. To identify potential treatments for OUD, we screened a targeted selection of over 100 drugs using a recently developed opioid self-administration assay in zebrafish. This paradigm showed that finasteride, a steroidogenesis inhibitor approved for the treatment of benign prostatic hyperplasia and androgenetic alopecia, reduced self-administration of multiple opioids without affecting locomotion or feeding behavior. These findings were confirmed in rats; furthermore, finasteride reduced the physical signs associated with opioid withdrawal. In rat models of neuropathic pain, finasteride did not alter the antinociceptive effect of opioids and reduced withdrawal-induced hyperalgesia. Steroidomic analyses of the brains of fish treated with finasteride revealed a significant increase in dehydroepiandrosterone sulfate (DHEAS). Treatment with precursors of DHEAS reduced opioid self-administration in zebrafish in a fashion akin to the effects of finasteride. These results highlight the importance of steroidogenic pathways as a rich source of therapeutic targets for OUD and point to the potential of finasteride as a new treatment option for this disorder.

Indexed as

5-alpha Reductase InhibitorsAnimalsDisease Models, AnimalFinasterideHumansMaleOpioid-Related DisordersRatsRats, Sprague-DawleyZebrafish5-alpha Reductase InhibitorsFinasterideAddictionDrug screensNeuroscience

Identifiers

PMID33848264
PMCPMC8121512
OpenAlexW3154437481

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.