Inhibition of nitric oxide synthase influences the activity of striatal neurons in the rat

Neurosci Lett. 2002 Jun 14;325(3):179-82. doi: 10.1016/s0304-3940(02)00270-7.

Abstract

The activity of single units in the striatum of urethane-anesthetized rats was recorded before and after the systemic administration of 7-nitro-indazole (7-NI; 50 mg/kg intraperitoneally), a selective inhibitor of neuronal nitric oxide (NO) synthase. Two neuronal types were clearly distinguishable electrophysiologically, on the basis of either discharge frequency pattern or features of the individual spike waveform (spike duration, negative phase/total duration ratio, and negative phase/total amplitude ratio). Only sporadically discharging neurons (basal firing rate, <0.1 spikes/s) were influenced by 7-NI, which caused a statistically significant increase in their firing rate. In contrast, the activity of continuously discharging neurons (basal firing rate, 4-6 spikes/s) was not affected. We hypothesize that NO neurotransmission could exert a tonic inhibitory influence upon sporadically discharging striatal neurons, which are presumably striatal output neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials
  • Animals
  • Corpus Striatum / drug effects*
  • Corpus Striatum / enzymology
  • Corpus Striatum / physiology
  • Electrophysiology
  • Enzyme Inhibitors / pharmacology
  • Indazoles / pharmacology
  • Male
  • Nerve Tissue Proteins / antagonists & inhibitors
  • Nitric Oxide / metabolism
  • Nitric Oxide / physiology*
  • Nitric Oxide Synthase / antagonists & inhibitors*
  • Nitric Oxide Synthase Type I
  • Rats
  • Rats, Wistar

Substances

  • Enzyme Inhibitors
  • Indazoles
  • Nerve Tissue Proteins
  • Nitric Oxide
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type I
  • Nos1 protein, rat
  • 7-nitroindazole