Platelet alpha-adrenergic binding and biochemical responsiveness in depressed patients and controls

  • Larry J. Siever
  • , Marian S. Kafka
  • , Steven Targum
  • , C. Raymond Lake

Research output: Contribution to journalArticlepeer-review

81 Scopus citations

Abstract

In a study of platelet α2-adrenergic receptor number in depressed patients, binding of tritiated dihydroergocriptine (3H-DHE) to platelet membranes was measured in 23 depressed patients and 51 controls. To examine the functional responsiveness of the platelet α2-adrenergic receptor, basal cyclic adenosine 3',5'- monophosphate (cAMP) production, prostaglandin E1 (PGE1) stimulation of cAMP production, and norepinephrine (NE) inhibition of PGE1-stimulated cAMP production were measured in 23 depressed patients and 53 control subjects. Finally, plasma NE concentration was measured in 20 patients to explore the possible relationship between this endogenous agonist and platelet α2-adrenergic receptor function. 3H-DHE binding to platelet membranes was significantly increased in the depressed patients compared to control subjects. Both the PGE1-stimulated cAMP response and the inhibition of this response by NE were significantly reduced in the depressed patients compared to the control subjects. Thus, an apparent dissociation between α2-adrenergic receptor binding and functional responsiveness was observed. Plasma NE concentrations were neither significantly different in the depressed patients than in the controls nor correlated with any of the measures of cAMP responsiveness. They were, however, significantly negatively correlated with 3H-DHE binding in depressed patients with adequate PGE1 stimulation of cAMP production.

Original languageEnglish
Pages (from-to)287-302
Number of pages16
JournalPsychiatry Research
Volume11
Issue number4
DOIs
StatePublished - Apr 1984
Externally publishedYes

Keywords

  • 5'-monophosphate
  • Platelet αadrenergic receptor
  • cyclic adenosine 3'
  • norepinephrine
  • prostaglandin E
  • tritiated dihydroergocriptine

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