Evidence map›Paper›PMID 42622700›Full record

ArticleJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2026

Low-Dose Cannabidiol Treatment does not Alter Cognitive Performance in the HIV-1 Transgenic Rat Model of NeuroHIV.

Samantha M Ayoub, Sunitha Vemuri, Arpi Minassian, Jared W Young

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Article in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Samantha M AyoubDepartment of Psychiatry, University of California San Diego, 9500 Gilman Drive MC 0804, La Jolla, San Diego, CA, 92093-0804, USA.ORCID http://orcid.org/0009-0006-1846-3232
Sunitha VemuriDepartment of Psychiatry, University of California San Diego, 9500 Gilman Drive MC 0804, La Jolla, San Diego, CA, 92093-0804, USA.
Arpi MinassianDepartment of Psychiatry, University of California San Diego, 9500 Gilman Drive MC 0804, La Jolla, San Diego, CA, 92093-0804, USA. aminassian@health.ucsd.edu.
Jared W YoungDepartment of Psychiatry, University of California San Diego, 9500 Gilman Drive MC 0804, La Jolla, San Diego, CA, 92093-0804, USA. jaredyoung@ucsd.edu.ORCID http://orcid.org/0000-0003-3732-5776

Funding

Translational Studies of Cannabis Administration, Cognition, and the Endocannabinoid System in HIVR01DA051295 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MINASSIAN, ARPI, YOUNG, JARED WILLIAM · 2021 to 2025
$4.3M
Immunometabolicgene expression profiles associated with depressed mood and behavioral domains inpeople with HIVR01MH128869 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLIS, RONALD J., YOUNG, JARED WILLIAM · 2021 to 2025
$3.6M
NIDA NIH HHS R01DA051295NIMH NIH HHS R01MH128869
6 · The paper itself

Abstract

backgroundHIV-associated neurocognitive impairment (NCI) remains prevalent among virally suppressed people living with HIV (PLWH) and approved treatments target these symptoms. Cannabidiol (CBD), a non-intoxicating cannabinoid with neuroprotective and anti-inflammatory properties, has been proposed as a potential therapeutic candidate for HIV-associated NCI, yet its cognitive effects in the context of HIV have not been experimentally tested.

methodsFemale and male HIV-1 transgenic (HIV-1Tg; n = 57) and Fischer 344 (F344; n = 57) control rats were assessed using a translational cognitive battery measuring risk-based decision-making (Iowa Gambling Task; IGT), learning and cognitive flexibility (Probabilistic Reversal Learning Task; PRLT), and effortful motivation (Progressive Ratio Breakpoint Task; PRBT). Animals were tested at baseline to establish innate cognitive performance, then retested following acute and chronic (16-day) CBD administration (0, 0.3, and 3 mg/kg).

resultsHIV-1Tg rats exhibited subtle IGT deficits and persistent reversal learning deficits in the PRLT, with preserved learning and motivation, modeling key features of HIV-associated NCI. These selective impairments in cognitive flexibility persisted across testing periods, with performance in other domains largely intact. CBD produced modest, dose-specific effects on response latencies and motivation but did not affect cognitive performance.

conclusionHIV-1Tg rats exhibited selective cognitive deficits similar to those seen in PLWH, supporting their utility as a preclinical model of HIV-associated NCI. Across multiple translatable cognitive domains CBD did not significantly alter cognitive performance in HIV-1Tg rats at the doses tested. Further research using broader dosing, different administration routes, and co-administration with other cannabinoids is needed to fully explore the therapeutic potential of CBD for targeting HIV-associated NCI.

Indexed as

AIDS Dementia ComplexCannabidiolCognitionHIV-1AnimalsDisease Models, AnimalDose-Response Relationship, DrugFemaleMaleRatsRats, Inbred F344Rats, TransgenicCannabidiolCognitive flexibilityDecision-makingLearningPhytocannabinoidTranslational animal model

Identifiers

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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 Socratic graph.