Rapid versus delayed stimulation of feeding by the endogenously released AgRP neuron mediators GABA, NPY, and AgRP.

Agouti-related peptide (AgRP) neurons of the hypothalamus release a fast transmitter (GABA) in addition to neuropeptides (neuropeptide Y [NPY] and Agouti-related peptide [AgRP]). This raises questions as to their respective functions. The acute activation of AgRP neurons robustly promotes food intake, while central injections of AgRP, NPY, or GABA agonist results in the marked escalation of food consumption with temporal variance. Given the orexigenic capability of all three of these neuroactive substances in conjunction with their coexpression in AgRP neurons, we looked to unravel their relative temporal role in driving food intake. After the acute stimulation of AgRP neurons with DREADD technology, we found that either GABA or NPY is required for the rapid stimulation of feeding, and the neuropeptide AgRP, through action on MC4 receptors, is sufficient to induce feeding over a delayed yet prolonged period. These studies help to elucidate the neurochemical mechanisms of AgRP neurons in controlling temporally distinct phases of eating.

[1]  B. Lowell,et al.  Synaptic release of GABA by AgRP neurons is required for normal regulation of energy balance , 2008, Nature Neuroscience.

[2]  S. Sternson,et al.  Hunger States Switch a Flip-Flop Memory Circuit via a Synaptic AMPK-Dependent Positive Feedback Loop , 2011, Cell.

[3]  G. Barsh,et al.  Effects of Hypothalamic Neurodegeneration on Energy Balance , 2005, PLoS biology.

[4]  A. N. van den Pol Neuropeptide transmission in brain circuits. , 2012, Neuron.

[5]  R. Palmiter,et al.  Response of melanocortin–4 receptor–deficient mice to anorectic and orexigenic peptides , 1999, Nature Genetics.

[6]  Thorsten Buch,et al.  Agouti-related peptide–expressing neurons are mandatory for feeding , 2005, Nature Neuroscience.

[7]  A. N. van den Pol,et al.  Neuropeptide Transmission in Brain Circuits , 2012, Neuron.

[8]  D. Macneil,et al.  Neither Agouti-Related Protein nor Neuropeptide Y Is Critically Required for the Regulation of Energy Homeostasis in Mice , 2002, Molecular and Cellular Biology.

[9]  Ann E. Kelley,et al.  GABA in the Nucleus Accumbens Shell Participates in the Central Regulation of Feeding Behavior , 1997, The Journal of Neuroscience.

[10]  M. Low,et al.  Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus , 2001, Nature.

[11]  R. Palmiter,et al.  Loss of GABAergic Signaling by AgRP Neurons to the Parabrachial Nucleus Leads to Starvation , 2009, Cell.

[12]  S. Sternson,et al.  AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training , 2010, Nature Neuroscience.

[13]  S. Bloom,et al.  A C-terminal fragment of Agouti-related protein increases feeding and antagonizes the effect of alpha-melanocyte stimulating hormone in vivo. , 1998, Endocrinology.

[14]  M. Nicolelis,et al.  Remote Control of Neuronal Activity in Transgenic Mice Expressing Evolved G Protein-Coupled Receptors , 2009, Neuron.

[15]  G. Barsh,et al.  Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein. , 1997, Science.

[16]  Robert A. McGovern,et al.  Divergence of Melanocortin Pathways in the Control of Food Intake and Energy Expenditure , 2005, Cell.

[17]  B. Roth,et al.  Rapid, reversible activation of AgRP neurons drives feeding behavior in mice. , 2011, The Journal of clinical investigation.

[18]  R. Palmiter,et al.  Sensitivity to leptin and susceptibility to seizures of mice lacking neuropeptide Y , 1996, Nature.

[19]  R. Palmiter,et al.  NPY/AgRP Neurons Are Essential for Feeding in Adult Mice but Can Be Ablated in Neonates , 2005, Science.

[20]  Bernardo L. Sabatini,et al.  Fasting Activation of AgRP Neurons Requires NMDA Receptors and Involves Spinogenesis and Increased Excitatory Tone , 2012, Neuron.

[21]  S. Bouret,et al.  Distinct Roles for Specific Leptin Receptor Signals in the Development of Hypothalamic Feeding Circuits , 2012, The Journal of Neuroscience.

[22]  A. N. van den Pol,et al.  Agouti-Related Peptide and MC3/4 Receptor Agonists Both Inhibit Excitatory Hypothalamic Ventromedial Nucleus Neurons , 2008, The Journal of Neuroscience.

[23]  J. Betley,et al.  Deconstruction of a neural circuit for hunger , 2012, Nature.

[24]  T. Hökfelt,et al.  The neuropeptide Y/agouti gene-related protein (AGRP) brain circuitry in normal, anorectic, and monosodium glutamate-treated mice. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[25]  Minmin Luo,et al.  Acute and Long-Term Suppression of Feeding Behavior by POMC Neurons in the Brainstem and Hypothalamus, Respectively , 2013, The Journal of Neuroscience.

[26]  P. Ramamoorthy,et al.  Cell Type-Dependent Trafficking of Neuropeptide Y-Containing Dense Core Granules in CNS Neurons , 2011, The Journal of Neuroscience.

[27]  R. Palmiter,et al.  Effects of neuropeptide Y deficiency on hypothalamic agouti-related protein expression and responsiveness to melanocortin analogues , 1999, Brain Research.

[28]  Mohammad A Ghatei,et al.  Coordinated changes in energy intake and expenditure following hypothalamic administration of neuropeptides involved in energy balance , 2009, International Journal of Obesity.

[29]  P S Kalra,et al.  Neuropeptide Y and human pancreatic polypeptide stimulate feeding behavior in rats. , 1984, Endocrinology.