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The Journal of Neurophysiology Vol. 88 No. 2 August 2002, pp. 817-828
Copyright ©2002 by the American Physiological Society
Mental Retardation Research Center, Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, California 90024-1759
Michel, Stephan,
Jason Itri, and
Christopher S. Colwell.
Excitatory Mechanisms in the Suprachiasmatic Nucleus: The
Role of AMPA/KA Glutamate Receptors. J. Neurophysiol. 88: 817-828, 2002. A variety of evidence suggests
that the effects of light on the mammalian circadian system are
mediated by direct retinal ganglion cell projection to the
suprachiasmatic nucleus (SCN). This synaptic connection is
glutamatergic and the release of glutamate is detected by both
N-methyl-D-asparate (NMDA) and amino-methyl proprionic acid/kainate (AMPA/KA) iontotropic glutamate receptors (GluRs). It is well established that NMDA GluRs play a critical role in
mediating the effects of light on the circadian system; however, the
role of AMPA/KA GluRs has received less attention. In the present
study, we sought to better understand the contribution of
AMPA/KA-mediated currents in the circadian system based in the SCN.
First, whole cell patch-clamp electrophysiological techniques were
utilized to measure spontaneous excitatory postsynaptic currents (sEPSCs) from SCN neurons. These currents were widespread in the SCN
and not just restricted to the retino-recipient region. The sEPSC
frequency and amplitude did not vary with the daily cycle. Similarly,
currents evoked by the exogenous application of AMPA onto SCN neurons
were widespread within the SCN and did not exhibit a diurnal rhythm in
their magnitude. Fluorometric techniques were utilized to estimate
AMPA-induced calcium (Ca2+) concentration changes
in SCN neurons. The resulting data indicate that AMPA-evoked
Ca2+ transients were widespread in the SCN and
that there was a daily rhythm in the magnitude of AMPA-induced
Ca2+ transients that peaked during the night. By
itself, blocking AMPA/KA GluRs with a receptor blocker decreased the
spontaneous firing of some SCN neurons as well as reduced resting
Ca2+ levels, suggesting tonic glutamatergic
excitation. Finally, immunohistochemical techniques were used to
describe expression of the AMPA-preferring GluR subunits GluR1 and
GluR2/3s within the SCN. Overall, our data suggest that glutamatergic
synaptic transmission mediated by AMPA/KA GluRs play an important role
throughout the SCN synaptic circuitry.
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