Evidence map›Paper›PMID 30710109›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2019

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

Aimilia Lydia Kalafateli, Daniel Vallöf, Giancarlo Colombo, Irene Lorrai, Paola Maccioni, Elisabet Jerlhag

Open access · hybridAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 14% of its field
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.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Amylin: A Multi-Functional Pancreatic Hormone-A Review.Diabetes, obesity & metabolism · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Calcitonin receptor signaling in nucleus accumbens D1R- and D2R-expressing medium spiny neurons bidirectionally alters opioid taking in male rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Environmental Factors That Affect Parathyroid Hormone and Calcitonin Levels.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 3 countries.

Aimilia Lydia KalafateliDepartment of Pharmacology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Daniel VallöfDepartment of Pharmacology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Giancarlo ColomboNeuroscience Institute, Section of Cagliari, National Research Council of Italy, Monserrato, CA, Italy.
Irene LorraiNeuroscience Institute, Section of Cagliari, National Research Council of Italy, Monserrato, CA, Italy.
Paola MaccioniNeuroscience Institute, Section of Cagliari, National Research Council of Italy, Monserrato, CA, Italy.
Elisabet JerlhagDepartment of Pharmacology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden. Elisabet.Jerlhag@pharm.gu.se.
University of Gothenburg · SENational Academies of Sciences, Engineering, and Medicine · USNational Research Council · IT

Funding

Sahlgrenska Universitetssjukhuset (Sahlgrenska University Hospital) 148251Vetenskapsrådet (Swedish Research Council) 2015-03219
6 · The paper itself

Abstract

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.

Indexed as

AlcoholismAlcohol DrinkingAmylin Receptor AgonistsAnimalsBehavior, AnimalCalcitoninDisease Models, AnimalDrinking BehaviorEatingMaleNucleus AccumbensPeptide FragmentsRatsRats, WistarReceptors, Islet Amyloid PolypeptideSelf AdministrationAC 187Amylin Receptor AgonistsCalcitoninPeptide FragmentsReceptors, Islet Amyloid Polypeptidesalmon calcitonin

Identifiers

PMID30710109
PMCPMC6461824
OpenAlexW2913572814

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.