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      Unraveling the Central Proopiomelanocortin Neural Circuits

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          Abstract

          Central proopiomelanocortin (POMC) neurons form a potent anorexigenic network, but our understanding of the integration of this hypothalamic circuit throughout the central nervous system (CNS) remains incomplete. POMC neurons extend projections along the rostrocaudal axis of the brain, and can signal with both POMC-derived peptides and fast amino acid neurotransmitters. Although recent experimental advances in circuit-level manipulation have been applied to POMC neurons, many pivotal questions still remain: how and where do POMC neurons integrate metabolic information? Under what conditions do POMC neurons release bioactive molecules throughout the CNS? Are GABA and glutamate or neuropeptides released from POMC neurons more crucial for modulating feeding and metabolism? Resolving the exact stoichiometry of signals evoked from POMC neurons under different metabolic conditions therefore remains an ongoing endeavor. In this review, we analyze the anatomical atlas of this network juxtaposed to the physiological signaling of POMC neurons both in vitro and in vivo. We also consider novel genetic tools to further characterize the function of the POMC circuit in vivo. Our goal is to synthesize a global view of the POMC network, and to highlight gaps that require further research to expand our knowledge on how these neurons modulate energy balance.

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          Most cited references162

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          Anatomy and regulation of the central melanocortin system.

          Roger Cone (2005)
          The central melanocortin system is perhaps the best-characterized neuronal pathway involved in the regulation of energy homeostasis. This collection of circuits is unique in having the capability of sensing signals from a staggering array of hormones, nutrients and afferent neural inputs. It is likely to be involved in integrating long-term adipostatic signals from leptin and insulin, primarily received by the hypothalamus, with acute signals regulating hunger and satiety, primarily received by the brainstem. The system is also unique from a regulatory point of view in that it is composed of fibers expressing both agonists and antagonists of melanocortin receptors. Given that the central melanocortin system is an active target for development of drugs for the treatment of obesity, diabetes and cachexia, it is important to understand the system in its full complexity, including the likelihood that the system also regulates the cardiovascular and reproductive systems.
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            Neuropeptide transmission in brain circuits.

            Neuropeptides are found in many mammalian CNS neurons where they play key roles in modulating neuronal activity. In contrast to amino acid transmitter release at the synapse, neuropeptide release is not restricted to the synaptic specialization, and after release, a neuropeptide may diffuse some distance to exert its action through a G protein-coupled receptor. Some neuropeptides such as hypocretin/orexin are synthesized only in single regions of the brain, and the neurons releasing these peptides probably have similar functional roles. Other peptides such as neuropeptide Y (NPY) are synthesized throughout the brain, and neurons that synthesize the peptide in one region have no anatomical or functional connection with NPY neurons in other brain regions. Here, I review converging data revealing a complex interaction between slow-acting neuromodulator peptides and fast-acting amino acid transmitters in the control of energy homeostasis, drug addiction, mood and motivation, sleep-wake states, and neuroendocrine regulation. Copyright © 2012 Elsevier Inc. All rights reserved.
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              Rapid rewiring of arcuate nucleus feeding circuits by leptin.

              The fat-derived hormone leptin regulates energy balance in part by modulating the activity of neuropeptide Y and proopiomelanocortin neurons in the hypothalamic arcuate nucleus. To study the intrinsic activity of these neurons and their responses to leptin, we generated mice that express distinct green fluorescent proteins in these two neuronal types. Leptin-deficient (ob/ob) mice differed from wild-type mice in the numbers of excitatory and inhibitory synapses and postsynaptic currents onto neuropeptide Y and proopiomelanocortin neurons. When leptin was delivered systemically to ob/ob mice, the synaptic density rapidly normalized, an effect detectable within 6 hours, several hours before leptin's effect on food intake. These data suggest that leptin-mediated plasticity in the ob/ob hypothalamus may underlie some of the hormone's behavioral effects.
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                Author and article information

                Journal
                Front Neurosci
                Front. Neurosci.
                Frontiers in Neuroscience
                Frontiers Media S.A.
                1662-4548
                1662-453X
                22 February 2013
                2013
                : 7
                : 19
                Affiliations
                [1] 1Department of Molecular and Integrative Physiology, University of Michigan Ann Arbor, MI, USA
                [2] 2Department of Biomedical Sciences, Colorado State University Fort Collins, CO, USA
                [3] 3Departments of Behavioral Neuroscience and Pathology, Oregon Health & Science University Portland, OR, USA
                [4] 4Research Services, Neurocytology Laboratory, Veterans Affairs Medical Center Portland, OR, USA
                [5] 5Department of Internal Medicine, Division of Metabolism, Endocrinology and Diabetes, University of Michigan Ann Arbor, MI, USA
                Author notes

                Edited by: Kevin W. Williams, The University of Texas Southwestern Medical Center, USA

                Reviewed by: Jennifer W. Hill, University of Toledo College of Medicine, USA; Marc Claret, Institut d’Investigacions Biomèdiques August Pi i Sunyer, Spain; Makoto Fukuda, Baylor College of Medicine, USA

                *Correspondence: Malcolm J. Low, Department of Molecular and Integrative Physiology, University of Michigan, 6116 Brehm Tower, 1000 Wall Street, Ann Arbor, MI 48105, USA. e-mail: mjlow@ 123456umich.edu

                This article was submitted to Frontiers in Neuroendocrine Science, a specialty of Frontiers in Neuroscience.

                Article
                10.3389/fnins.2013.00019
                3579188
                23440036
                cb07829d-f0ee-4fbe-b395-bc02f4ea0cff
                Copyright © 2013 Mercer, Hentges, Meshul and Low.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 19 November 2012
                : 04 February 2013
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 170, Pages: 12, Words: 13244
                Categories
                Neuroscience
                Review Article

                Neurosciences
                arcuate nucleus,energy homeostasis,hypothalamus,metabolism,neural networks,obesity,proopiomelanocortin neurons

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