Different effects of the calcium antagonists nimodipine and flunarizine on dopamine metabolism in the rat brain

J Neural Transm. 1989;75(3):195-200. doi: 10.1007/BF01258630.

Abstract

The effect of two calcium antagonists, nimodipine and flunarizine, on striatal dopamine (DA) metabolism in rats was compared. Flunarizine (5-20 mg/kg i.p.) caused a dose-dependent increase in the DA metabolite, 3,4-dihydroxyphenylacetic acid (DOPAC) in the caudate nucleus. Following the 20 mg/kg dose, DOPAC levels were maximally elevated by about 50% from 2 to 12 hrs after treatment. On the contrary, nimodipine at the dose of 20 mg/kg i.p. produced a modest decrease in DOPAC levels. Neither calcium antagonist modified DA content. However, both nimodipine and flunarizine, at the dose of 20 mg/kg, markedly reduced the accumulation of DOPAC in the caudate nucleus induced by haloperidol (1 mg/kg). It is suggested that flunarizine, but not nimodipine, has a neuroleptic-like action, whereas the two calcium antagonists have in common the ability to attenuate the hyperactivity of DA neurons.

MeSH terms

  • 3,4-Dihydroxyphenylacetic Acid / metabolism
  • Animals
  • Calcium Channel Blockers / pharmacology*
  • Caudate Nucleus / drug effects
  • Caudate Nucleus / metabolism*
  • Dopamine / metabolism*
  • Dose-Response Relationship, Drug
  • Flunarizine / pharmacology*
  • Haloperidol / pharmacology
  • Male
  • Nimodipine / pharmacology*
  • Rats
  • Rats, Inbred Strains

Substances

  • Calcium Channel Blockers
  • 3,4-Dihydroxyphenylacetic Acid
  • Nimodipine
  • Haloperidol
  • Flunarizine
  • Dopamine