Effect of amygdaloid kindling on [3H]dopamine and [14C]acetylcholine release from rat prefrontal cortex and striatal slices

Matti Mintz*, Louise Reyneke, Anna de Villiers, Rosemary Allin, Vivienne Russell, William Daniels, Gian van der Spuy, Abdullah Jaffer, Lauriston Kellaway, Rodney Douglas, Joshua Taljaard

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


The involvement of the dopaminergic (DA) systems in the control of limbic kindled seizures is ill defined. The effects of kindling on DA activity may have been overlooked in the past, because of its subtle unilateral occurrence and/or the variance of the endogenous imbalance of DA activity in normal animals. In the present study rats were screened for their endogenous DA imbalance using amphetamine-induced rotational behaviour. Electrical or sham kindling was applied in the hemisphere with the higher endogenous DA activity. Sections of the bilateral prefrontal cortex and dorsal and ventral striatum were dissected either 2 hours or 21 days after the final seizure and the electrically stimulated release of [3H]DA and [14C]acetylcholine (ACh) determined. Release was also measured in the presence of quinpirole or sulpiride to assess the activity of pre- and postsynaptic DA D2-receptors. Long-term effects of kindling consisted of facilitation of ACh release in the ventral striatum contralateral to the kindled amygdala and bilateral depression of DA release in the prefrontal cortex. Kindling therefore produced area specific changes in neurotransmitter systems giving rise to increased pro-convulsive cholinergic activity in the ventral striatum and decreased anti-convulsive dopaminergic activity in the prefrontal cortex.

Original languageEnglish
Pages (from-to)115-121
Number of pages7
JournalBrain Research
Issue number1-2
StatePublished - 2 Oct 1992


  • Acetylcholine
  • Amygdala
  • Dopamine
  • Dopamine D receptor
  • Kindling
  • Prefrontal cortex
  • Release
  • Striatum
  • Superfusion


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