Long latency event-related potentials in rats: effects of dopaminergic and serotonergic depletions

Pharmacol Biochem Behav. 1991 Apr;38(4):789-93. doi: 10.1016/0091-3057(91)90243-u.

Abstract

The effects of serotonergic and dopaminergic depletions on event-related potentials (ERPs) generated by an auditory "oddball" paradigm were evaluated. Eighteen rats received either sham or six-hydroxydopamine (6-OHDA) lesions to the ventral tegmental area (VTA), and were subsequently implanted with electrodes in the frontal cortex, dorsal hippocampus (DHPC), and amygdala (AMYG). In these animals, a series of large amplitude potentials in the 10-200 ms latency range could be recorded from all the brain areas tested. In addition, late positivities (in the 300-400 ms range) were identified in DHPC and AMYG. 6-OHDA lesions to the VTA were found to produce a 30-46% reduction in dopamine, but did not significantly alter any of the ERP components. A second series of rats were implanted with electrodes in cortex and DHPC. These rats then received vehicle injections and subsequently injections of parachlorophenylalanine (PCPA). PCPA produced a 50% depletion of serotonin concomitant with significant reductions in the negative components in the 50-100 ms range recorded in hippocampus and cortex. These studies support a role for serotonin but not dopamine in the processing of passively presented auditory stimuli and further suggest that the rat may be a good model for the exploration of long latency ERPs.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amygdala / drug effects
  • Amygdala / physiology
  • Animals
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / physiology
  • Dopamine / physiology*
  • Electrophysiology
  • Evoked Potentials, Auditory / drug effects
  • Evoked Potentials, Auditory / physiology*
  • Fenclonine / pharmacology
  • Hippocampus / drug effects
  • Hippocampus / physiology
  • Male
  • Rats
  • Rats, Inbred Strains
  • Serotonin / physiology*

Substances

  • Serotonin
  • Fenclonine
  • Dopamine