An amylin analogue attenuates alcohol-related behaviours in various animal models of alcohol use disorder

• Published in: Neuropsychopharmacology (New York, N.Y.) N.Y.), 2019-05, Vol.44 (6), p.1093-1102
• Main Authors: Kalafateli, Aimilia Lydia, Vallöf, Daniel, Colombo, Giancarlo, Lorrai, Irene, Maccioni, Paola, Jerlhag, Elisabet
• Format: Article
• Language: English
• Subjects: Alcohol; Alcohol Drinking; Alcohol use; Alcoholic beverages; Alcoholism; Alcohols; Amylin; Amylin Receptor Agonists - administration & dosage; Amylin Receptor Agonists - pharmacology; Animal models; Animals; Behavior, Animal - drug effects; Calcitonin; Calcitonin - administration & dosage; Calcitonin - pharmacology; Chocolate; Disease Models, Animal; Dopamine; Drinking behavior; Drinking Behavior - drug effects; Drug self-administration; Eating - drug effects; Food intake; Low alcohol; Male; Mesolimbic system; Neurosciences; Neurovetenskaper; Nucleus accumbens; Nucleus Accumbens - metabolism; Operant conditioning; Peptide Fragments - administration & dosage; Peptide Fragments - pharmacology; Rats; Rats, Wistar; Receptors, Islet Amyloid Polypeptide - antagonists & inhibitors; Receptors, Islet Amyloid Polypeptide - metabolism; Reinforcement; Rodents; Salmon; Schedules; Self Administration
• ISSN: 0893-133X; 1740-634X; 1740-634X
• DOI: 10.1038/s41386-019-0323-x

Recent findings have identified salmon calcitonin (sCT), an amylin receptor agonist and analogue of endogenous amylin, as a potential regulator of alcohol-induced activation of the mesolimbic dopamine system and alcohol consumption. Providing that the role of amylin signalling in alcohol-related behaviours remains unknown, the present experiments investigate the effect of sCT on these behaviours and the mechanisms involved. We showed that repeated sCT administration decreased alcohol and food intake in outbred rats. Moreover, single administration of the potent amylin receptor antagonist, AC187, increased short-term alcohol intake in outbred alcohol-consuming rats, but did not affect food intake. Acute administration of sCT prevented relapse-like drinking in the "alcohol deprivation effect" model in outbred alcohol-experienced rats. Additionally, acute sCT administration reduced operant oral alcohol self-administration (under the fixed ratio 4 schedule of reinforcement) in selectively bred Sardinian alcohol-preferring rats, while it did not alter operant self-administration (under the progressive ratio schedule of reinforcement) of a highly palatable chocolate-flavoured beverage in outbred rats. Lastly, we identified differential amylin receptor expression in high compared to low alcohol-consuming rats, as reflected by decreased calcitonin receptor and increased receptor activity modifying protein 1 expression in the nucleus accumbens (NAc) of high consumers. Collectively, our data suggest that amylin signalling, especially in the NAc, may contribute to reduction of various alcohol-related behaviours.