Cellular mechanisms of the slow (

Abstract:

:The slow (<1 Hz) rhythm is a defining feature of the electroencephalogram during sleep. Since cortical circuits can generate this rhythm in isolation, it is assumed that the accompanying slow oscillation in thalamocortical (TC) neurons is largely a passive reflection of neocortical activity. Here we show, however, that by activating the metabotropic glutamate receptor (mGluR), mGluR1a, cortical inputs can recruit intricate cellular mechanisms that enable the generation of an intrinsic slow oscillation in TC neurons in vitro with identical properties to those observed in vivo. These mechanisms rely on the "window" component of the T-type Ca(2+) current and a Ca(2+)-activated, nonselective cation current. These results suggest an active role for the thalamus in shaping the slow (<1 Hz) sleep rhythm.

journal_name

Neuron

journal_title

Neuron

authors

Hughes SW,Cope DW,Blethyn KL,Crunelli V

doi

10.1016/s0896-6273(02)00623-2

subject

Has Abstract

pub_date

2002-03-14 00:00:00

pages

947-58

issue

6

eissn

0896-6273

issn

1097-4199

pii

S0896627302006232

journal_volume

33

pub_type

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