EEG Correlation of the Discharge Properties of Identified Neurons in the Basal Forebrain

  1 Center for Molecular and Behavioral Neuroscience, Rutgers, The State University of New Jersey, Newark, New Jersey 07102; and   2 Department of Comparative Physiology, Eotvos Lorand University, H-1088 Budapest, Hungary Duque, A., B. Balatoni, L. Detari, and L. Zaborszky. EEG Correlation of the Di...

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Veröffentlicht in:Journal of neurophysiology 2000-09, Vol.84 (3), p.1627-1635
Hauptverfasser: Duque, A, Balatoni, B, Detari, L, Zaborszky, L
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Sprache:eng
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Zusammenfassung:  1 Center for Molecular and Behavioral Neuroscience, Rutgers, The State University of New Jersey, Newark, New Jersey 07102; and   2 Department of Comparative Physiology, Eotvos Lorand University, H-1088 Budapest, Hungary Duque, A., B. Balatoni, L. Detari, and L. Zaborszky. EEG Correlation of the Discharge Properties of Identified Neurons in the Basal Forebrain. J. Neurophysiol. 84: 1627-1635, 2000. The basal forebrain (BF) is a heterogeneous structure located in the ventral aspect of the cerebral hemispheres. It contains cholinergic as well as different types of noncholinergic corticopetal neurons and interneurons, including GABAergic and peptidergic cells. The BF constitutes an extrathalamic route to the cortex, and its activity is associated with an increase in cortical release of the neurotransmitter acetylcholine, concomitant with electroencephalographic (EEG) low-voltage fast activity (LVFA). However, the specific role of the different BF cell types has largely remained unknown due to the lack of chemical identification of the recorded neurons. Here we show that the firing rate of immunocytochemically identified cholinergic and parvalbumin-containing neurons increase during cortical LVFA. In contrast, increased neuropeptide Y neuron firing is accompanied by cortical slow waves. Our results, furthermore, indicate that BF neurons posses a distinct temporal relationship to different EEG patterns and suggest a more dynamic interplay within BF as well as between BF and cortical circuitries than previously proposed.
ISSN:0022-3077
1522-1598
DOI:10.1152/jn.2000.84.3.1627