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Group II metabotropic glutamate receptors in anxiety circuitry: Correspondence of physiological response and subcellular distribution
Author(s) -
Muly E. Chris,
Mania Irakli,
Guo JiDong,
Rainnie Donald G.
Publication year - 2007
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.21525
Subject(s) - metabotropic glutamate receptor , metabotropic glutamate receptor 2 , neuroscience , postsynaptic potential , biology , excitatory postsynaptic potential , stria terminalis , neurotransmission , basolateral amygdala , glutamate receptor , inhibitory postsynaptic potential , amygdala , receptor , biochemistry
Activation of group II metabotropic glutamate receptors (mGluR2/3) in the amygdala plays a critical role in the regulation of fear and anxiety states. Previous studies using nonselective agonists have suggested this action can result from activation of either pre‐ or postsynaptic mGluR2/3. Here, we have used a combination of whole‐cell patch clamp recording with highly selective agonists (LY354740 and LY379268) and immunoelectron microscopy to examine structure‐function relationships for mGluR2/3 in the basolateral amygdala (BLA) and bed nucleus of the stria terminalis (BNST). Stimulation of mGluR2/3 evoked a direct, TTX‐insensitive membrane hyperpolarization in all BLA projection neurons tested, but only about half of BNST neurons. The membrane hyperpolarization was mediated by activation of an outward potassium current or blockade of a tonically active inward I h current in different groups of BLA neurons. In both regions, mGluR2/3 caused a long‐lasting reduction of glutamate release from presynaptic afferent terminals even at concentrations that failed to elicit a direct postsynaptic response. The localization of mGluR2/3 differed regionally, with postsynaptic labeling significantly more common in BLA than BNST, corresponding to the strength of postsynaptic responses recorded there. Our results demonstrate a complex role for mGluR2/3 receptors in modulating anxiety circuitry, including direct inhibition and reduction of excitatory drive. The combination of direct inhibition of projection neurons within the BLA and suppression of excitatory neurotransmission in the BNST may be responsible for the anxiolytic actions of group II mGluR agonists. J. Comp. Neurol. 505:682–700, 2007. © 2007 Wiley‐Liss, Inc.