Agmatine reverses ethanol consumption in rats: Evidences for an interaction with imidazoline receptors

• Published in: Pharmacology, biochemistry and behavior Vol. 186; p. 172779
• Main Authors: Taksande, Brijesh G., Nambiar, Shreesha, Patil, Shardha, Umekar, Milind J., Aglawe, Manish M., Kotagale, Nandkishor R.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.11.2019
• Subjects: Agmatine; Agmatine - pharmacology; Alcohol Drinking; Animals; Conditioning, Operant; Ethanol - administration & dosage; Ethanol consumption; Female; Imidazoline receptors; Imidazoline Receptors - drug effects; Male; Operant conditioning; Rats; Rats, Wistar; Self Administration; Two bottle choice paradigm; Imidazoline receptors; Ethanol consumption; Operant conditioning; Agmatine; Two bottle choice paradigm
• ISSN: 0091-3057; 1873-5177
• DOI: 10.1016/j.pbb.2019.172779

Alcohol is one of the most widely abused recreational drugs, largely linked with serious health and social concerns. However, the treatment options for alcohol-use disorders have limited efficacy and exhibit a range of adverse drug reactions. Large numbers of preclinical studies have projected a biogenic amine, agmatine as a promising potential treatment option for drug addiction, including alcoholism. In the present study, administration of agmatine (20–40 mg/kg, i.p.) resulted in significant inhibition of ethanol self-administration in the right p-VTA in operant conditioning paradigm. Further, acute intracranial administration of agmatine (20 and 40 μg/rat) significantly reduced the ethanol consumption in the two bottle choice paradigm. Agmatine is degraded to putrescine and guanido-butanoic acid by the enzyme agmatinase and diamine oxidase respectively and inhibition of these enzymes results in augmentation of endogenous agmatine. In the present study, diamine oxidase inhibitor, aminoguanidine and agmatinase inhibitor, arcaine were used to block the agmatine metabolic pathways to increase brain agmatine levels. Drugs that augment endogenous agmatine levels like L-arginine (80 μg/rat, i.c.v.) or arcaine (50 μg/rat, i.c.v.) and aminoguanidine (25 μg/rat, i.c.v.) also reduced the ethanol consumption following their central administration. The pharmacological effect of agmatine on ethanol consumption was potentiated by imidazoline receptor agonists, I1 agonist moxonidine (25 μg/rat, i.c.v.), and imidazoline I2 agonist, 2-BFI (10 μg/rat, i.c.v.) and was blocked by imidazoline I1 antagonist, efaroxan (10 μg/rat, i.c.v.), and I2 antagonist, idazoxan (4 μg/rat, i.c.v.) at their ineffective doses per se. Thus, our result suggests the involvement of imidazoline I1 and I2 receptors in agmatine induced inhibition of ethanol consumption in rats. •Agmatine inhibited ethanol self-administration in operant conditioning paradigm.•Intracranial administration of agmatine reduced the ethanol consumption in the two bottle choice paradigm.•Agmatinergic agents reduced the ethanol consumption.•Imidazoline receptor agonists potentiated and antagonists blocked the effect of agmatine on ethanol consumption.