Literature DB >> 28088358

The peroxisome proliferator-activated receptor alpha agonist fenofibrate attenuates alcohol self-administration in rats.

Colin N Haile1, Therese A Kosten2.   

Abstract

Fibrates are a class of medications used to treat hypercholesterolemia and dyslipidemia that target nuclear peroxisome proliferator-activated receptors (PPARs). Studies have shown the PPARα agonist fenofibrate decreases voluntary EtOH consumption however its impact on the reinforcing and motivational effects of EtOH is unknown. We evaluated the ability of fenofibrate (25, 50 and 100 mg/kg), to alter EtOH (10%, w/v) and sucrose (2%, w/v) operant self-administration in rats under a FR2 schedule of reinforcement over four days and under a progressive ratio (PR) schedule on day five of treatment. Results showed fenofibrate dose-dependently decreased EtOH self-administration under both schedules of reinforcement with the greatest effects seen after four to five days of treatment. Fenofibrate decreased responding for sucrose only under the PR schedule of reinforcement and this effect was not dose-dependent. These findings provide further evidence for fenofibrate as a potential treatment for alcohol use disorder in humans.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Addiction; Alcohol; Drug seeking; Ethanol; Ethanol reinforcement; PPARα; Peroxisome proliferator-activated receptors; Progressive ratio; Rats; Self-administration

Mesh:

Substances:

Year:  2017        PMID: 28088358      PMCID: PMC5385150          DOI: 10.1016/j.neuropharm.2017.01.007

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  39 in total

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Journal:  Pharmacol Rev       Date:  2006-12       Impact factor: 25.468

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Authors:  Therese A Kosten
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Journal:  Nature       Date:  2001-11-08       Impact factor: 49.962

5.  Cannabinoids and PPARalpha signalling.

Authors:  Y Sun; S P H Alexander; D A Kendall; A J Bennett
Journal:  Biochem Soc Trans       Date:  2006-12       Impact factor: 5.407

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Journal:  J Neurosci       Date:  2013-04-03       Impact factor: 6.167

7.  Fenofibrate--a lipid-lowering drug--reduces voluntary alcohol drinking in rats.

Authors:  Eduardo Karahanian; Maria Elena Quintanilla; Katia Fernandez; Yedy Israel
Journal:  Alcohol       Date:  2014-08-20       Impact factor: 2.405

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9.  Ethanol-derived acetaldehyde: pleasure and pain of alcohol mechanism of action.

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Journal:  Curr Drug Targets       Date:  2013-06       Impact factor: 3.465

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4.  The GABAB receptor positive allosteric modulator ASP8062 reduces operant alcohol self-administration in male and female Sprague Dawley rats.

Authors:  Colin N Haile; Benjamin A Carper; Tracy L Nolen; Therese A Kosten
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Review 5.  Medications for alcohol use disorders: An overview.

Authors:  Mohammed Akbar; Mark Egli; Young-Eun Cho; Byoung-Joon Song; Antonio Noronha
Journal:  Pharmacol Ther       Date:  2017-12-02       Impact factor: 12.310

Review 6.  Neuroimmune signaling in alcohol use disorder.

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7.  Beta-caryophyllene inhibits cocaine  addiction-related behavior by activation of PPARα and PPARγ: repurposing a FDA-approved food additive for cocaine use disorder.

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Review 8.  Therapeutic Potential of Peroxisome Proliferator-Activated Receptor (PPAR) Agonists in Substance Use Disorders: A Synthesis of Preclinical and Human Evidence.

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Journal:  Cells       Date:  2020-05-12       Impact factor: 6.600

Review 9.  Immune treatments for alcohol use disorder: A translational framework.

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10.  Peroxisome Proliferator Activated Receptor Agonists Modulate Transposable Element Expression in Brain and Liver.

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