The Ca2+ channel blockade changes the behavioral and biochemical effects of immobilization stress

Neuropsychopharmacology. 1999 Mar;20(3):248-54. doi: 10.1016/S0893-133X(98)00071-2.

Abstract

We investigated how the effects of chronic immobilization stress in rats are modified by Ca2+ channel blockade preceding restraint sessions. The application of nifedipine (5 mg/kg) shortly before each of seven daily 2 h restraint sessions prevented the development of sensitized response to amphetamine as well as the stress-induced elevation of the densities of L-type Ca2+ channel in the hippocampus and significantly reduced the elevation of the densities of [3H]nitrendipine binding sites in the cortex and D1 dopamine receptors in the limbic forebrain. Neither stress, nor nifedipine affected the density of alpha 1-adrenoceptors and D1 receptors in the cerebral cortex nor D2 dopamine receptors in the striatum. A single restraint session caused an elevation of blood corticosterone level that remained unaffected by nifedipine pretreatment, but the reduction of this response during the eighth session was significantly less expressed in nifedipine-treated rats. We conclude that L-type calcium channel blockade prevents development of several stress-induced adaptive responses.

MeSH terms

  • Amphetamine / pharmacology
  • Animals
  • Calcium Channel Blockers / pharmacology*
  • Calcium Channels / metabolism
  • Central Nervous System Stimulants / pharmacology
  • Cerebral Cortex / metabolism
  • Corpus Striatum / metabolism
  • Corticosterone / blood
  • Hippocampus / metabolism
  • Hyperkinesis / chemically induced
  • Hyperkinesis / prevention & control
  • Immobilization*
  • Male
  • Nifedipine / pharmacology*
  • Prosencephalon / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, Adrenergic, alpha-1 / metabolism
  • Receptors, Dopamine D1 / metabolism
  • Receptors, Dopamine D2 / metabolism
  • Stress, Physiological / drug therapy*
  • Stress, Physiological / metabolism

Substances

  • Calcium Channel Blockers
  • Calcium Channels
  • Central Nervous System Stimulants
  • Receptors, Adrenergic, alpha-1
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Amphetamine
  • Nifedipine
  • Corticosterone