Evidence map›Paper›PMID 39975399›Full record

ArticlebioRxiv : the preprint server for biology2025

Chronic intermittent ethanol produces nociception through endocannabinoid-independent mechanisms in mice.

C Miliano, Y Dong, M Proffit, N Corvalan, L A Natividad, A M Gregus, M W Buczynski

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

C MilianoSchool of Neuroscience, Virginia Polytechnic and State University, 970 Washington Street SW, Blacksburg, VA 24061.
Y DongSchool of Neuroscience, Virginia Polytechnic and State University, 970 Washington Street SW, Blacksburg, VA 24061.
M ProffitSchool of Neuroscience, Virginia Polytechnic and State University, 970 Washington Street SW, Blacksburg, VA 24061.
N CorvalanSchool of Neuroscience, Virginia Polytechnic and State University, 970 Washington Street SW, Blacksburg, VA 24061.
L A NatividadCollege of Pharmacy, Division of Pharmacology and Toxicology, University of Texas at Austin, Austin, Texas, USA.
A M GregusSchool of Neuroscience, Virginia Polytechnic and State University, 970 Washington Street SW, Blacksburg, VA 24061.
M W BuczynskiSchool of Neuroscience, Virginia Polytechnic and State University, 970 Washington Street SW, Blacksburg, VA 24061.

Funding

15-LOX-1 as a druggable target in the acute to chronic pain transition of rheumatoid arthritisR01AR075241 · NIAMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI GREGUS, ANN MARIE · 2019 to 2023
$1.7M
Anti-nociceptive actions of CART II in chemotherapy-induced peripheral neuropathyR01CA284075 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI Matthew Wallace Buczynski · 2023 to 2026
$1.4M
The role of the OEA synthase NAPE-PLD in nicotine signaling and rewardR00DA035865 · NIDA · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI BUCZYNSKI, MATTHEW WALLACE · 2017 to 2019
$747k
NCI NIH HHS R01 CA284075NIAMS NIH HHS R01 AR075241NIDA NIH HHS R00 DA035865
6 · The paper itself

Abstract

Alcohol use disorder (AUD) affects millions of people and represents a significant health and economic burden. Pain represents a frequently under-treated aspect of hyperkatifeia during alcohol withdrawal, yet to date no drugs have received FDA approval for the treatment of this indication in AUD patients. This study aims to evaluate the potential of targeting bioactive lipid signaling pathways as a therapeutic approach for treating alcohol withdrawal-related pain. We utilized a chronic intermittent ethanol (CIE) vapor exposure model in C57BL/6J mice of both sexes to establish alcohol dependence, and demonstrated that CIE mice developed robust tactile allodynia and thermal hyperalgesia during withdrawal that was independent of prior blood alcohol levels. Next, we evaluated four drugs for their efficacy in reversing tactile allodynia during abstinence from CIE using a cross-over treatment design that included FDA-approved naltrexone as well as commercially available inhibitors targeting inflammatory lipid signaling enzymes including fatty acid amide hydrolase (FAAH), monoacylglycerol lipase (MAGL), and 15-Lipoxygenase (LOX). None of these compounds produced significant therapeutic benefit in reversing established CIE-induced tactile allodynia, despite attenuating pain-like behaviors at these doses in other chronic pain models. Additionally, we assessed plasma endocannabinoid levels in both sexes during withdrawal. We found that there is an inherent sex difference in the endogenous anti-inflammatory endocannabinoid tone in naive mice and CIE treatment affected endocannabinoids levels in female mice only. These findings underscore the need to better understand the driving causes of AUD induced pain and to develop novel therapeutic approaches to mitigate pain in AUD patients.

Identifiers

PMID39975399
PMCPMC11838487

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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.