Neurochemical and neuropharmacological investigations with four ergot derivatives: bromocriptine, dihydroergotoxine, CF 25-397 and CM 29-712

Pharmacology. 1978:16 Suppl 1:156-73. doi: 10.1159/000136817.

Abstract

Neurochemical and neuropharmacological investigations with four ergot derivatives reveal differential pharmacodynamic effects of these compounds. Bromocriptine and CM 29-712 showed actions typical of postsynaptic dopamine receptor stimulants, in particular in the extrapyramidal system. CM 29-712 proved to be more potent than bromocriptine, with an early onset of action. CF 25-397 and dihydroergotoxine, while not showing all actions typical of central dopamine agonists, appeared to exert some of their effects by means of a stimulation of central serotoninergic sites. In the rat sleep-wakefulness cycles and in reserpine-induced ponto-geniculooccipital waves in the cat, they mimicked the effects of 5-hydroxytryptophan. In the latter test, CF 25-397 proved to be particularly potent. In addition, bromocriptine, dihydroergotoxine and CM 29-712 showed neurochemical effects consistent with central alpha-adrenergic blockade or an enhanced impulse flow in central noradrenergic neurons.

MeSH terms

  • Animals
  • Behavior, Animal / drug effects
  • Brain / metabolism
  • Bromocriptine / pharmacology
  • Catecholamines / metabolism
  • Chemical Phenomena
  • Chemistry
  • Dihydroergotoxine / pharmacology*
  • Electroencephalography
  • Ergolines / pharmacology*
  • Humans
  • Locomotion / drug effects
  • Male
  • Mice
  • Morphine / antagonists & inhibitors
  • Movement Disorders / chemically induced
  • Rabbits
  • Rats
  • Receptors, Dopamine / drug effects
  • Reserpine
  • Sleep / drug effects
  • Stereotyped Behavior / drug effects

Substances

  • Catecholamines
  • Ergolines
  • Receptors, Dopamine
  • Dihydroergotoxine
  • Bromocriptine
  • Morphine
  • Reserpine