Skip to main navigation Skip to search Skip to main content

Platelet adenylyl cyclase activity as a biochemical trait marker for predisposition to alcoholism

  • Joëlle E. Ratsma
  • , W. Boudewijn Gunning
  • , Rob Leurs
  • , Anton N. M. Schoffelmeer
  • University of Amsterdam
  • Vrije Universiteit Amsterdam

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Previous studies demonstrated a reduced G(s)-protein stimulated adenylyl cyclase activity in the brain and blood cells of alcoholics. We investigated this phenomenon in platelets of children of alcoholics (COA), i.e., of children at high risk for the acquisition of alcoholism and (as yet) not regularly consuming alcohol. G(s)-protein mediated stimulation of adenylyl cyclase by 30 mM NaF and 50 μM forskolin stimulated adenylyl cyclase activity were assessed in platelet membranes of 23 (male and female) COA and 20 control children. G(s)-protein stimulated cAMP production by NaF, unlike that induced by direct stimulation of adenylyl cyclase with forskolin, in platelet membranes of COA was profoundly lower than in platelet membranes of control children. Moreover, such a reduced G(s)-protein functioning was only observed in platelet membranes of COA with a multigenerational family history of alcoholism. A reduction of G(s)protein stimulated adenylyl cyclase activity, in platelets may represent a sensitive and gender-independent trait marker for predisposition to alcoholism, rather than a state marker for alcoholism.
Original languageEnglish
Pages (from-to)600-604
JournalAlcoholism, clinical and experimental research
Volume23
Issue number4
DOIs
Publication statusPublished - Apr 1999
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Platelet adenylyl cyclase activity as a biochemical trait marker for predisposition to alcoholism'. Together they form a unique fingerprint.

Cite this