Evidence map›Paper›PMID 38838083›Full record

ArticleAlcohol, clinical & experimental research2024

Bilateral insular cortical lesions reduce sensitivity to the adverse consequences of acute ethanol intoxication in Pavlovian conditioning procedures.

Ashmita Mukherjee, Elizabeth A Gilles-Thomas, Hay Young Kwok, Cerissa E Shorter, Kajol V Sontate, Shannon L McSain, Sarah C Honeycutt, Gregory C Loney

Abstract read
In one paragraph

Article in Alcohol, clinical & experimental research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing 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.

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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

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ashmita MukherjeeProgram in Behavioral Neuroscience, Department of Psychology, State University of New York, University at Buffalo, Buffalo, New York, USA.
Elizabeth A Gilles-ThomasProgram in Behavioral Neuroscience, Department of Psychology, State University of New York, University at Buffalo, Buffalo, New York, USA.
Hay Young KwokProgram in Behavioral Neuroscience, Department of Psychology, State University of New York, University at Buffalo, Buffalo, New York, USA.
Cerissa E ShorterProgram in Behavioral Neuroscience, Department of Psychology, State University of New York, University at Buffalo, Buffalo, New York, USA.
Kajol V SontateProgram in Behavioral Neuroscience, Department of Psychology, State University of New York, University at Buffalo, Buffalo, New York, USA.
Shannon L McSainProgram in Behavioral Neuroscience, Department of Psychology, State University of New York, University at Buffalo, Buffalo, New York, USA.
Sarah C HoneycuttProgram in Behavioral Neuroscience, Department of Psychology, State University of New York, University at Buffalo, Buffalo, New York, USA.
Gregory C LoneyProgram in Behavioral Neuroscience, Department of Psychology, State University of New York, University at Buffalo, Buffalo, New York, USA.ORCID https://orcid.org/0000-0003-3936-1885

Funding

Social Anxiety, Stress and Ethanol Sensitivity in Adolescence and AdulthoodP50AA017823 · NIAAA · UPSTATE MEDICAL UNIVERSITY · PI J. DAVID JENTSCH · 2009 to 2026
$30.5M
RESEARCH TRAINING ON ALCOHOL ETIOLOGY AND TREATMENTT32AA007583 · NIAAA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Gregory G Homish, KENNETH E LEONARD · 2000 to 2026
$8.5M
Nicotinic and Insular Cortical Mechanisms Contributing to Opiate MisuseK01DA048336 · NIDA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI LONEY, GREGORY CARL · 2019 to 2024
$860k
NIAAA NIH HHS AA007583NIAAA NIH HHS AA017823NIAAA NIH HHS P50 AA017823NIAAA NIH HHS T32 AA007583NIDA NIH HHS DA048336NIDA NIH HHS K01 DA048336
6 · The paper itself

Abstract

backgroundSensitivity to the adverse post-ingestive effects of ethanol likely serves as a deterrent to initiate alcohol consumption early in drinking and later may contribute to efforts to remain abstinent. Administering ethanol to naïve rats prior to Pavlovian conditioning procedures elicits robust ethanol-conditioned taste and place avoidance (CTA; CPA) mediated by its subjective interoceptive properties. The insular cortex (IC) has been implicated as a region involved in mediating sensitivity to the interoceptive properties of ethanol. Here, we examined whether bilateral lesions of the IC affect the acquisition and expression of taste and place avoidance in ethanol-induced CTA and CPA paradigms.

methodsAdult male and female Wistar rats received bilateral excitotoxic lesions (ibotenic acid; 20 mg/mL; 0.3 μL) of the IC prior to conditioning procedures. Subsequently, rats were conditioned to associate a novel taste stimulus (0.1% saccharin) and context with the effects of ethanol (1.0 g/kg) in a combined CTA/CPP procedure. Conditioning occurred over 8 alternating CS+/CS- days, followed by tests for expression of taste and place preferences. Data from IC-lesioned rats were compared with neurologically intact rats.

resultsOur findings revealed that neurologically intact rats showed a significantly stronger ethanol-induced CTA than IC-lesioned rats. There were no significant differences in total fluid intake when rats consumed water (CS-). As with CTA effects, intact rats showed a strong CPA, marked by a greater reduction in time spent on the drug-paired context, while IC-lesioned rats failed to display CPA to ethanol.

conclusionThese results indicate that proper IC functioning is necessary for responding to the adverse interoceptive properties of ethanol regardless of which Pavlovian paradigm is used to assess interoceptive responsivity to ethanol. Blunted IC functioning from chronic ethanol use may reduce interoceptive signaling specifically of ethanol's adverse effects thus contributing to increased alcohol use.

Indexed as

alcoholaversiveconditioninginteroceptionPavlovian

Identifiers

PMID38838083
PMCPMC12648566

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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.