Characterization of nitric oxide generator-induced hippocampal [3H]norepinephrine release. I. The role of glutamate

G. Lonart, K. M. Johnson

Research output: Contribution to journalArticle

51 Scopus citations

Abstract

In this study we compared the effects of two nitrogen monoxide (NO) generators, hydroxylamine and S-nitroso-L-cysteine (NO-CYS), on hippocampal [3H]norepinephrine ([3H]NE) release. A 10-min incubation with hydroxylamine (3-3,000 μM) or NO-CYS (30-10,000 μM) induced a concentration-dependent increase in the basal [3H]NE efflux with EC50 values of approximately 100 μM and 1 mM, respectively. Reduced hemoglobin, a NO scavenger, blocked both hydroxylamine- and NO-CYS-evoked [3H]NE release. Long-term exposure (≥25 min) to 100 μM hydroxylamine, or to millimolar concentrations of NO-CYS, evoked a tetrodotoxin-insensitive [3H]NE release. However, a 10-min stimulation with either 100 μM hydroxylamine or 300 μM NO-CYS was sensitive to 0.5 μM tetrodotoxin, a voltage-sensitive sodium channel blocker. This suggested that under these conditions hydroxylamine and NO-CYS induce [3H]NE release indirectly in part, perhaps via releasing an excitatory neurotransmitter. Indeed, kynurenate, a nonselective ionotropic glutamate receptor antagonist, produced an 80% inhibition of the NO generator-evoked [3H]NE release. CGS 19755, a N-methyl-D-aspartate receptor antagonist, had no significant effect, whereas the α-amino-3-hydroxy-5-methylisoxazole-4- propionic acid/kainate receptor antagonists, CNQX and GYKI 52446, inhibited the hydroxylamine response by 50%. In synaptosomes, a preparation in which synaptic interactions are nonsignificant, NO-CYS induced a dose-dependent release of both [3H]NE and [3H]glutamate. These data suggest that, in hippocampal slices, NO generators evoke [3H]NE release both directly from noradrenergic terminals and indirectly via releasing glutamate.

Original languageEnglish (US)
Pages (from-to)7-13
Number of pages7
JournalJournal of Pharmacology and Experimental Therapeutics
Volume275
Issue number1
StatePublished - Jan 1 1995

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

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