4.7 Article

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

Journal

NEUROPSYCHOPHARMACOLOGY
Volume 44, Issue 6, Pages 1093-1102

Publisher

SPRINGERNATURE
DOI: 10.1038/s41386-019-0323-x

Keywords

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Funding

  1. Novo Nordisk Foundation
  2. Swedish Research Council [2015-03219]
  3. Swedish Society for Medical Research
  4. Swedish brain foundation
  5. LUA/ALF from the Sahlgrenska University Hospital [148251]
  6. Alcohol research council of the Swedish alcohol retailing monopoly
  7. foundation of Adlerbertska
  8. foundation of Fredrik and Ingrid Thuring
  9. foundation of Tore Nilsson
  10. foundation of Langmanska
  11. foundation of Wilhelm and Martina Lundgren
  12. foundation of Knut and Alice Wallenberg
  13. foundation of Magnus Bergvall
  14. foundation of Aners
  15. foundation of Jeansons
  16. foundation of Ake Wiberg
  17. foundation of Novo Nordisk
  18. foundation of Swedish Society of Medicin
  19. Torsten Soderberg
  20. Vinnova [2015-03219] Funding Source: Vinnova
  21. Swedish Research Council [2015-03219] Funding Source: Swedish Research Council

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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.

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