Manuel Mattheisen

αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  • Alanna C Easton, MRC Social, Genetic and Developmental Psychiatry Research Centre, Institute of Psychiatry, King's College London, London, UK., Denmark
  • Walter Lucchesi, Denmark
  • Anbarasu Lourdusamy
  • ,
  • Bernd Lenz, Denmark
  • Jalal Solati, Denmark
  • Yulia Golub, Denmark
  • Piotr Lewczuk
  • ,
  • Cathy Fernandes, Denmark
  • Sylvane Desrivieres, Denmark
  • Ralph R Dawirs, Denmark
  • Gunther H Moll, Denmark
  • Johannes Kornhuber
  • ,
  • Josef Frank
  • ,
  • Per Hoffmann
  • ,
  • Michael Soyka
  • ,
  • Falk Kiefer
  • ,
  • Gunter Schumann
  • ,
  • K Peter Giese, Denmark
  • Christian P Müller, Denmark
  • Jens Treutlein
  • ,
  • Sven Cichon
  • ,
  • Monika Ridinger
  • ,
  • Manuel Mattheisen
  • Stefan Herms
  • ,
  • Norbert Wodarz
  • ,
  • Peter Zill
  • ,
  • Wolfgang Maier
  • ,
  • Rainald Mössner
  • ,
  • Wolfgang Gaebel
  • ,
  • Norbert Dahmen
  • ,
  • Norbert Scherbaum
  • ,
  • Christine Schmäl
  • ,
  • Michael Steffens
  • ,
  • Susanne Lucae
  • ,
  • Marcus Ising
  • ,
  • Bertram Müller-Myhsok
  • ,
  • Markus M Nöthen
  • ,
  • Karl Mann
  • ,
  • Marcella Rietschel
  • ,
  • GESGA Consortium
  • ,
  • Manuel Mattheisen

The α-Ca(2+)/calmodulin-dependent protein kinase II (αCaMKII) is a crucial enzyme controlling plasticity in the brain. The autophosphorylation of αCaMKII works as a 'molecular memory' for a transient calcium activation, thereby accelerating learning. We investigated the role of αCaMKII autophosphorylation in the establishment of alcohol drinking as an addiction-related behavior in mice. We found that alcohol drinking was initially diminished in αCaMKII autophosphorylation-deficient αCaMKII(T286A) mice, but could be established at wild-type level after repeated withdrawals. The locomotor activating effects of a low-dose alcohol (2 g/kg) were absent in αCaMKII(T286A) mice, whereas the sedating effects of high-dose (3.5 g/kg) were preserved after acute and subchronic administration. The in vivo microdialysis revealed that αCaMKII(T286A) mice showed no dopamine (DA) response in the nucleus accumbens to acute or subchronic alcohol administration, but enhanced serotonin (5-HT) responses in the prefrontal cortex. The attenuated DA response in αCaMKII(T286A) mice was in line with altered c-Fos activation in the ventral tegmental area after acute and subchronic alcohol administration. In order to compare findings in mice with the human condition, we tested 23 single-nucleotide polymorphisms (SNPs) in the CAMK2A gene for their association with alcohol dependence in a population of 1333 male patients with severe alcohol dependence and 939 controls. We found seven significant associations between CAMK2A SNPs and alcohol dependence, one of which in an autophosphorylation-related area of the gene. Together, our data suggest αCaMKII autophosphorylation as a facilitating mechanism in the establishment of alcohol drinking behavior with changing the DA-5-HT balance as a putative mechanism.

Original languageEnglish
JournalNeuropsychopharmacology
Volume38
Issue9
Pages (from-to)1636-47
Number of pages12
ISSN0893-133X
DOIs
Publication statusPublished - Aug 2013

    Research areas

  • Alcohol Drinking, Alcoholism, Animals, Behavior, Addictive, Calcium-Calmodulin-Dependent Protein Kinase Type 2, Case-Control Studies, Dopamine, Dose-Response Relationship, Drug, Ethanol, Female, Genetic Predisposition to Disease, Humans, Hypnotics and Sedatives, Male, Mice, Motor Activity, Nucleus Accumbens, Phosphorylation, Polymorphism, Single Nucleotide, Prefrontal Cortex, Serotonin, Ventral Tegmental Area

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