Norepinephrine induces pathway-specific long-lasting potentiation and depression in the hippocampal dentate gyrus.

Abstract

The study presented here indicates that norepinephrine (NE) selectively induced long-lasting modifications of synaptically mediated responses in the dentate gyrus of the rat hippocampal slice. A low concentration of NE (1.0 .mu.M; in the presence of 50 .mu.M phentolamine, an .alpha.-adrenergic antagonist) or a 1.0 .mu.M concentration of the specific .beta.-adrenergic agonist isoproterenol induced long-lasting pathway-specific alterations of granule cell electrophysiological responses. Excitatory postsynaptic potentials and population spikes evoked by stimulation of the medial perforant pathway (PP) were potentiated for more than 45 min. In contrast, responses to lateral PP stimulation were depressed for the same period. Both potentiation and depression were blocked by the .beta.-adrenergic antagonist propranolol (1.0 .mu.M). These results indicate that NE can act differentially on projections to the dentate gyrus arising in the entorhinal cortex. Such selective persistent modifications of cortical circuits may be involved in processes in the mammalian brain underlying attention, learning, and memory.