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J Neurophysiol 99: 77-86, 2008. First published October 31, 2007; doi:10.1152/jn.00902.2007
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Cortical-Like Functional Organization of the Pheromone-Processing Circuits in the Medial Amygdala

Xiling Bian1,2, Yuchio Yanagawa3, Wei R. Chen4 and Minmin Luo2

1Institute of Biophysics, Chinese Academy of Sciences; 2National Institute of Biological Sciences, Beijing, China; 3Department of Genetic and Behavioral Neuroscience, Gunma University Graduate School of Medicine and Solution Oriented Research for Science and Technology, Japan Science and Technology Corporation, Maebashi, Japan; and 4Department of Neurobiology, Yale University Medical Center, New Haven, Connecticut

Submitted 13 August 2007; accepted in final form 25 October 2007

The medial amygdala (MeA) is a critical center for processing pheromonal signals that regulate social and reproductive behaviors, but the fundamental cellular mechanisms underlying signal processing in the MeA have remained largely unknown. Some studies suggest that the MeA belongs to the striatum and provides inhibitory output to hypothalamic areas including the ventromedial hypothalamus (VMH). By combining tract tracing, genetic labeling of GABAergic neurons, and immunostaining against markers for glutamatergic synapses, we found that a majority of MeA neurons projecting to the VMH are glutamatergic. Whole cell patch-clamp recordings revealed that VMH-projecting neurons form a homogeneous population in terms of morphological and intrinsic properties. Nearly all cells possess Ih and IT and in some cases they can give rise to postinhibitory rebound spikes. Morphological analysis of neurobiotin-filled cells revealed neurons with long dendritic arbors that extend to the MeA external layer and within the amygdala. Thus the VMH-projecting neurons in the MeA differ from the medium spiny neurons, the principal neurons of striatum, in terms of intrinsic physiological properties and morphology. In contrast, they resemble a subset of pyramidal cells in deep piriform cortex. Similar to pyramidal cells in piriform cortex, the VMH-projecting neurons in the MeA received direct excitatory input from their upstream sensory areas and inhibitory input from local GABAergic neurons. We conclude that pheromonal signals relayed to the VMH are processed by unique cortical, but not striatal, circuitry in the MeA.


Address for reprint requests and other correspondence: M. Luo, National Institute of Biological Sciences, #7 Science Park Rd., Zhongguancun Life Science Park, Beijing, 102206, China (E-mail: luominmin{at}nibs.ac.cn)







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