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The Journal of Neuroscience, February 18, 2004, 24(7):1578-1583; doi:10.1523/JNEUROSCI.3952-03.2004

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Cellular/Molecular
GABA Release from Proopiomelanocortin Neurons

Shane T. Hentges,1 Mitsuru Nishiyama,2 Linda S. Overstreet,1 Mary Stenzel-Poore,2 John T. Williams,1 and Malcolm J. Low1,3,4

1Vollum Institute, 2Department of Molecular Microbiology and Immunology, 3Department of Behavioral Neuroscience, and 4Center for the Study of Weight Regulation and Associated Disorders, Oregon Health and Science University, Portland, Oregon 97239

Neural networks controlling food intake and energy homeostasis clearly involve proopiomelanocortin (POMC) neurons and their peptide transmitters. {alpha}-melanocyte-stimulating hormone from arcuate POMC neurons potently reduces food intake, whereas arcuate neuropeptide Y (NPY) neurons act in opposition to stimulate food intake. In addition to orexigenic peptides, NPY neurons also release the inhibitory neurotransmitter GABA, which can act in a local circuit to inhibit POMC neuron activity. Whether or not reciprocal inhibition could occur has not yet been determined, because the presence of a rapid neurotransmitter in POMC neurons has not been demonstrated previously. Here, we used primary cultures of fluorescently labeled POMC neurons that had formed recurrent synapses (autapses) to detect the release of neurotransmitter. When an action potential was evoked in the axon of a POMC neuron with autapses, a short-latency synaptic current was recorded in the same cell. The autaptic current was abolished by GABAA receptor antagonists and substantially inhibited by opioids. Double-label in situ RNA hybridization for POMC and glutamic acid decarboxylase, the GABA synthetic enzyme, revealed colocalization of mRNAs in approximately one-third of POMC neurons in vivo. Our results suggest that these neurons can exert rapid inhibitory effects via the release of GABA, in addition to the more sustained actions provided by POMC peptides. However, this rapid inhibition may not play a major role within local hypothalamic circuits, but rather is likely to be important in more distant projection areas as indicated by the colocalization of vesicular GABA transporter immunoreactivity predominately in extrahypothalamic POMC terminals.

Key words: arcuate nucleus; opioids; neuron culture; hypothalamus; autapse; transgenic mouse; green fluorescent protein


Received Aug 26, 2003; revised December 9, 2003; accepted December 15, 2003.




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