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The Journal of Neurophysiology Vol. 87 No. 1 January 2002, pp. 558-566
Copyright ©2002 by the American Physiological Society
1Department of Neurological Surgery and 2The Graduate Program in Neuroscience, University of California, San Francisco, California 94143; and 3Howard Hughes Medical Institute, University of Washington, Seattle, Washington 98195
Guo, Hui,
Peter A. Castro,
Richard D. Palmiter, and
Scott C. Baraban.
Y5 Receptors Mediate Neuropeptide Y Actions at Excitatory
Synapses in Area CA3 of the Mouse Hippocampus. J. Neurophysiol. 87: 558-566, 2002. Neuropeptide Y (NPY) is a
potent modulator of excitatory synaptic transmission and limbic
seizures. NPY is abundantly expressed in the dentate gyrus and is
thought to modulate hippocampal excitability via activation of
presynaptic Y2 receptors (Y2R). Here we demonstrate that NPY, and
commonly used Y2R-preferring (NPY13-36) and Y5
receptor (Y5R)-preferring
([D-Trp32]NPY and hPP) peptide
agonists, evoke similar levels of inhibition at excitatory CA3 synapses
in hippocampal slices from wild-type control mice (WT). In contrast,
NPYergic inhibition of excitatory CA3 synaptic transmission is absent
in mice lacking the Y5R subtype (Y5R KO). In both analyses of evoked
population spike activity and spontaneous excitatory postsynaptic
synaptic currents (EPSCs), NPY agonists induced powerful inhibitory
effects in all hippocampal slices from WT mice, whereas these peptides
had no effect in slices from Y5R KO mice. In slices from WT mice, NPY
(and NPY receptor-preferring agonists) reduced the frequency of
spontaneous EPSCs but had no effect on sEPSC amplitude, rise time, or
decay time. Furthermore, NPYergic modulation of spontaneous EPSCs in WT
mice was mimicked by bath application of a novel Y5R-selective peptide
agonist ([cpp]hPP) but not the selective Y2R agonist
([ahx5-24]NPY). In situ hybridization was used
to confirm the presence of NPY, Y2, and Y5 mRNA in the hippocampus of
WT mice and the absence of Y5R in knockout mice. These results suggest
that the Y5 receptor subtype, previously believed to mediate food
intake, plays a critical role in modulation of hippocampal excitatory transmission at the hilar-to-CA3 synapse in the mouse.
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