Academic Journal
A Scoping Review of Preclinical Paradigms for Clinically Tested Medications in Alcohol Use Disorder.
| Τίτλος: | A Scoping Review of Preclinical Paradigms for Clinically Tested Medications in Alcohol Use Disorder. |
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| Συγγραφείς: | Nieto SJ; Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, Michigan, USA.; Department of Psychology, University of California at Los Angeles, Los Angeles, California, USA., Donato S; Department of Psychology, University of California at Los Angeles, Los Angeles, California, USA., Baskerville WA; Department of Psychology, University of California at Los Angeles, Los Angeles, California, USA., McManus KR; Department of Psychology, University of California at Los Angeles, Los Angeles, California, USA., Lopez MF; Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina, USA., Becker HC; Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina, USA., Ray LA; Department of Psychology, University of California at Los Angeles, Los Angeles, California, USA.; Department of Psychiatry and Biobehavioral Sciences, University of California at Los Angeles, Los Angeles, California, USA. |
| Πηγή: | Alcohol, clinical & experimental research [Alcohol Clin Exp Res (Hoboken)] 2026 May; Vol. 50 (5), pp. e70287. |
| Τύπος έκδοσης: | Journal Article; Scoping Review; Review |
| Γλώσσα: | English |
| Στοιχεία περιοδικού: | Publisher: Wiley Periodicals Country of Publication: United States NLM ID: 9918609780906676 Publication Model: Print Cited Medium: Internet ISSN: 2993-7175 (Electronic) Linking ISSN: 29937175 NLM ISO Abbreviation: Alcohol Clin Exp Res (Hoboken) Subsets: MEDLINE |
| Imprint Name(s): | Original Publication: Hoboken, NJ : Wiley Periodicals, [2023]- |
| Ιατρικοί όροι (MeSH): | Alcoholism*/drug therapy , Alcoholism*/psychology , Alcohol Deterrents*/therapeutic use, Drug Evaluation, Preclinical/methods ; Conditioning, Operant/drug effects ; Alcohol Drinking/drug therapy ; Alcohol Drinking/psychology ; Animals ; Humans ; Female ; Male ; Disease Models, Animal ; Rats |
| Περίληψη: | Despite increasing attention to the neurobiology of alcohol use disorder (AUD), development of effective pharmacotherapies remains limited. Many medications with promising preclinical profiles fail to translate into clinical efficacy. This scoping review characterizes preclinical studies evaluating medications for AUD that have also been tested in human laboratory paradigms or clinical trials. We focus on two widely used paradigms: the two-bottle choice (2BC) task, which measures alcohol consumption and preference, and operant reinstatement models, which capture relapse-like behavior. A systematic search and data extraction identified preclinical studies using 2BC and reinstatement paradigms to evaluate medications that progressed to human testing. Study characteristics (species, strain, sex, outcomes, and sample sizes) were recorded and effect sizes (corrected Cohen's d) were summarized across outcome domains. Ninety-two unique studies met criteria: 74 employing the 2BC paradigm and 18 using operant reinstatement models, including 1731 animals. Rats were the most common species and sex bias was pronounced: 77 2BC studies using only males, five only females, and all 18 reinstatement studies used male rats exclusively. For 2BC consumption, the largest effects were observed for medications with limited studies, such as levetiracetam (d = -4.58), while more extensively tested medications showed moderate effects, including prazosin (d = -0.74) and naltrexone (d = -0.63). For 2BC preference, levetiracetam again showed a large effect in a single study (d = -4.29). In reinstatement models, rimonabant showed the largest effect (d = -3.11), while naltrexone (d = -0.70), baclofen (d = -1.05), and varenicline (d = -0.72) had moderate effects. This review highlights substantial heterogeneity in study design and underutilization of reinstatement and female animals. Medications with moderate, replicable preclinical effects, especially those tested across both 2BC and reinstatement models, may hold greater translational promise. These findings offer key opportunities for enhancing the translational alignment of preclinical AUD pharmacotherapy research. (© 2026 Research Society on Alcohol.) |
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| Grant Information: | K24AA025704 United States AA NIAAA NIH HHS; R21AA029771 United States AA NIAAA NIH HHS; F32AA029288 United States AA NIAAA NIH HHS; R01AA029701-01S1 United States AA NIAAA NIH HHS |
| Contributed Indexing: | Keywords: alcohol use disorder; pharmacotherapy; preclinical models; reinstatement; rodent studies; scoping review; translational research; two‐bottle choice |
| Substance Nomenclature: | 0 (Alcohol Deterrents) |
| Entry Date(s): | Date Created: 20260508 Date Completed: 20260716 Latest Revision: 20260716 |
| Update Code: | 20260716 |
| DOI: | 10.1111/acer.70287 |
| PMID: | 42101829 |
| Βάση Δεδομένων: | MEDLINE |
| ISSN: | 2993-7175 |
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| DOI: | 10.1111/acer.70287 |