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Computational Analysis of the Hypothalamic Control of Food Intake

https://doi.org/10.3389/fncom.2016.00027

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.23273openalex-snapshot

Neurochemical characterization of neurons expressing melanin‐concentrating hormone receptor 1 in the mouse hypothalamus

inferredcites →https://doi.org/10.1002/syn.10075openalex-snapshot

“Nonhedonic” food motivation in humans involves dopamine in the dorsal striatum and methylphenidate amplifies this effect

inferredcites →https://doi.org/10.1007/978-1-4471-0043-0openalex-snapshot

Understanding Formal Methods

inferredcites →https://doi.org/10.1016/j.appet.2008.06.009openalex-snapshot

Body energy homeostasis

inferredcites →https://doi.org/10.1016/j.biopsych.2009.10.030openalex-snapshot

Ghrelin Increases the Rewarding Value of High-Fat Diet in an Orexin-Dependent Manner

inferredcites →https://doi.org/10.1016/j.biopsych.2012.10.026openalex-snapshot

Presynaptic Leptin Action Suppresses Excitatory Synaptic Transmission onto Ventral Tegmental Area Dopamine Neurons

inferredcites →https://doi.org/10.1016/j.biopsych.2014.06.008openalex-snapshot

Neuropeptide Y Activity in the Nucleus Accumbens Modulates Feeding Behavior and Neuronal Activity

inferredcites →https://doi.org/10.1016/j.brainres.2003.08.036openalex-snapshot

Oxytocin innervation of caudal brainstem nuclei activated by cholecystokinin

inferredcites →https://doi.org/10.1016/j.brainres.2004.11.008openalex-snapshot

Effects of fasting, leptin, and insulin on AGRP and POMC peptide release in the hypothalamus

inferredcites →https://doi.org/10.1016/j.cell.2005.08.035openalex-snapshot

Divergence of Melanocortin Pathways in the Control of Food Intake and Energy Expenditure

inferredcites →https://doi.org/10.1016/j.cell.2008.10.043openalex-snapshot

N-acylphosphatidylethanolamine, a Gut- Derived Circulating Factor Induced by Fat Ingestion, Inhibits Food Intake

inferredcites →https://doi.org/10.1016/j.cell.2013.11.002openalex-snapshot

Parallel, Redundant Circuit Organization for Homeostatic Control of Feeding Behavior

inferredcites →https://doi.org/10.1016/j.cell.2014.12.026openalex-snapshot

Visualizing Hypothalamic Network Dynamics for Appetitive and Consummatory Behaviors

inferredcites →https://doi.org/10.1016/j.cell.2015.01.033openalex-snapshot

Sensory Detection of Food Rapidly Modulates Arcuate Feeding Circuits

inferredcites →https://doi.org/10.1016/j.cmet.2009.06.011openalex-snapshot

Leptin Acts via Leptin Receptor-Expressing Lateral Hypothalamic Neurons to Modulate the Mesolimbic Dopamine System and Suppress Feeding

inferredcites →https://doi.org/10.1016/j.cmet.2009.10.009openalex-snapshot

Endogenous Leptin Signaling in the Caudal Nucleus Tractus Solitarius and Area Postrema Is Required for Energy Balance Regulation

inferredcites →https://doi.org/10.1016/j.cmet.2010.09.013openalex-snapshot

Glucose Stimulation of Hypothalamic MCH Neurons Involves KATP Channels, Is Modulated by UCP2, and Regulates Peripheral Glucose Homeostasis

inferredcites →https://doi.org/10.1016/j.cmet.2011.06.016openalex-snapshot

Leptin Action via Neurotensin Neurons Controls Orexin, the Mesolimbic Dopamine System and Energy Balance

inferredcites →https://doi.org/10.1016/j.mcn.2014.08.001openalex-snapshot

Metabolic regulation of lateral hypothalamic glucose-inhibited orexin neurons may influence midbrain reward neurocircuitry

inferredcites →https://doi.org/10.1016/j.molmet.2013.07.008openalex-snapshot

Loss of neurotensin receptor-1 disrupts the control of the mesolimbic dopamine system by leptin and promotes hedonic feeding and obesity

inferredcites →https://doi.org/10.1016/j.neuron.2006.06.004openalex-snapshot

Serotonin Reciprocally Regulates Melanocortin Neurons to Modulate Food Intake

inferredcites →https://doi.org/10.1016/j.neuron.2006.08.023openalex-snapshot

Leptin Receptor Signaling in Midbrain Dopamine Neurons Regulates Feeding

inferredcites →https://doi.org/10.1016/j.neuron.2008.09.033openalex-snapshot

5-HT2CRs Expressed by Pro-Opiomelanocortin Neurons Regulate Energy Homeostasis

inferredcites →https://doi.org/10.1016/j.neuron.2011.05.028openalex-snapshot

Leptin Action on GABAergic Neurons Prevents Obesity and Reduces Inhibitory Tone to POMC Neurons

inferredcites →https://doi.org/10.1016/j.neuropharm.2009.07.001openalex-snapshot

The acute and subchronic effects of a brain-penetrating, neurotensin-1 receptor agonist on feeding, body weight and temperature

inferredcites →https://doi.org/10.1016/j.neuroscience.2010.02.002openalex-snapshot

The role of orexin-A in food motivation, reward-based feeding behavior and food-induced neuronal activation in rats

inferredcites →https://doi.org/10.1016/j.npep.2012.09.004openalex-snapshot

Arcuate NPY neurons sense and integrate peripheral metabolic signals to control feeding

inferredcites →https://doi.org/10.1016/j.physbeh.2005.10.007openalex-snapshot

The rise, fall, and resurrection of the ventromedial hypothalamus in the regulation of feeding behavior and body weight

inferredcites →https://doi.org/10.1016/j.physbeh.2011.04.046openalex-snapshot

Glutamate and GABA in lateral hypothalamic mechanisms controlling food intake

inferredcites →https://doi.org/10.1016/j.tins.2013.05.003openalex-snapshot

Neuronal circuits that regulate feeding behavior and metabolism

inferredcites →https://doi.org/10.1016/s0006-8993(00)02125-9openalex-snapshot

Effect of chronic intraperitoneal injections of leptin on hypothalamic neurotensin content and food intake

inferredcites →https://doi.org/10.1016/s0031-9384(01)00589-3openalex-snapshot

Male and female 5-HT1B receptor knockout mice have higher body weights than wildtypes

inferredcites →https://doi.org/10.1016/s0092-8674(00)80949-6openalex-snapshot

Orexins and Orexin Receptors: A Family of Hypothalamic Neuropeptides and G Protein-Coupled Receptors that Regulate Feeding Behavior

inferredcites →https://doi.org/10.1016/s0166-4328(97)00140-xopenalex-snapshot

Specific changes in food intake elicited by blockade or activation of glutamate receptors in the nucleus accumbens shell

inferredcites →https://doi.org/10.1016/s0306-4522(01)00614-5openalex-snapshot

Presynaptic action of neurotensin on cultured ventral tegmental area dopaminergic neurones

inferredcites →https://doi.org/10.1016/s0889-8553(21)00440-4openalex-snapshot

Role of Cholecystokinin in the Control of Food Intake

inferredcites →https://doi.org/10.1016/s0896-6273(01)80035-0openalex-snapshot

Leptin Differentially Regulates NPY and POMC Neurons Projecting to the Lateral Hypothalamic Area

inferredcites →https://doi.org/10.1016/s0896-6273(03)00063-1openalex-snapshot

The Distribution and Mechanism of Action of Ghrelin in the CNS Demonstrates a Novel Hypothalamic Circuit Regulating Energy Homeostasis

inferredcites →https://doi.org/10.1016/s1043-2760(99)00153-8openalex-snapshot

The Central Melanocortin System and Energy Homeostasis

inferredcites →https://doi.org/10.1017/cbo9780511810275openalex-snapshot

Logic in Computer Science

inferredcites →https://doi.org/10.1037/h0028390openalex-snapshot

Relationship of body weight to the lateral hypothalamic feeding syndrome.

inferredcites →https://doi.org/10.1038/1082openalex-snapshot

Coexpression of Agrp and NPY in fasting-activated hypothalamic neurons

inferredcites →https://doi.org/10.1038/35078085openalex-snapshot

Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus

inferredcites →https://doi.org/10.1038/374542a0openalex-snapshot

Eating disorder and epilepsy in mice lacking 5-HT2C serotonin receptors

inferredcites →https://doi.org/10.1038/nature04071openalex-snapshot

A role for lateral hypothalamic orexin neurons in reward seeking

inferredcites →https://doi.org/10.1038/nature05026openalex-snapshot

Central nervous system control of food intake and body weight

inferredcites →https://doi.org/10.1038/nature11270openalex-snapshot

Deconstruction of a neural circuit for hunger

inferredcites →https://doi.org/10.1038/nm.2724openalex-snapshot

Leptin action through hypothalamic nitric oxide synthase-1–expressing neurons controls energy balance

inferredcites →https://doi.org/10.1038/nn.2664openalex-snapshot

5-HT2CRs expressed by pro-opiomelanocortin neurons regulate insulin sensitivity in liver

inferredcites →https://doi.org/10.1038/nn.2739openalex-snapshot

AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training

inferredcites →https://doi.org/10.1038/nn.3522openalex-snapshot

Optogenetic identification of a rapid eye movement sleep modulatory circuit in the hypothalamus

inferredcites →https://doi.org/10.1038/nn1548openalex-snapshot

Agouti-related peptide–expressing neurons are mandatory for feeding

inferredcites →https://doi.org/10.1046/j.1463-1326.2002.00234.xopenalex-snapshot

Orexin reverses cholecystokinin‐induced reduction in feeding

inferredcites →https://doi.org/10.1053/gast.2003.50020openalex-snapshot

Localization of orexin-1 receptors to vagal afferent neurons in the rat and humans

inferredcites →https://doi.org/10.1073/pnas.0802687105openalex-snapshot

Adaptive sugar sensors in hypothalamic feeding circuits

inferredcites →https://doi.org/10.1073/pnas.1407843111openalex-snapshot

MC4R-expressing glutamatergic neurons in the paraventricular hypothalamus regulate feeding and are synaptically connected to the parabrachial nucleus

inferredcites →https://doi.org/10.1097/00002826-199201001-00364openalex-snapshot

CONDITIONED RELEASE OF NEUROTRANSMITTERS AS MEASURED BY MICRODIALYSIS

inferredcites →https://doi.org/10.1111/j.1369-1600.2006.00002.xopenalex-snapshot

PRECLINICAL STUDY: Ghrelin stimulates locomotor activity and accumbal dopamine‐overflow via central cholinergic systems in mice: implications for its involvement in brain reward

inferredcites →https://doi.org/10.1111/j.1369-1600.2008.00125.xopenalex-snapshot

PRECLINICAL STUDY: Systemic administration of ghrelin induces conditioned place preference and stimulates accumbal dopamine

inferredcites →https://doi.org/10.1111/j.1467-789x.2006.00270.xopenalex-snapshot

The role of leptin and ghrelin in the regulation of food intake and body weight in humans: a review

inferredcites →https://doi.org/10.1111/j.1749-6632.1993.tb19746.xopenalex-snapshot

Contrasting Actions of Melanin‐Concentrating Hormone and Neuropeptide‐E‐I on Posterior Pituitary Function

inferredcites →https://doi.org/10.1126/science.1124147openalex-snapshot

Hypothalamic mTOR Signaling Regulates Food Intake

inferredcites →https://doi.org/10.1126/science.132.3422.301openalex-snapshot

Eating or Drinking Elicited by Direct Adrenergic or Cholinergic Stimulation of Hypothalamus

inferredcites →https://doi.org/10.1126/science.280.5368.1378openalex-snapshot

Signals That Regulate Food Intake and Energy Homeostasis

inferredcites →https://doi.org/10.1152/ajpendo.00205.2012openalex-snapshot

Endogenous leptin receptor signaling in the medial nucleus tractus solitarius affects meal size and potentiates intestinal satiation signals

inferredcites →https://doi.org/10.1152/ajpendo.00643.2012openalex-snapshot

Leptin receptor neurons in the mouse hypothalamus are colocalized with the neuropeptide galanin and mediate anorexigenic leptin action

inferredcites →https://doi.org/10.1152/ajpregu.00044.2011openalex-snapshot

Evidence for the role of hindbrain orexin-1 receptors in the control of meal size

inferredcites →https://doi.org/10.1152/ajpregu.00479.2002openalex-snapshot

Glucagon-like peptide 1-(7–36) amide acts at lateral and medial hypothalamic sites to suppress feeding in rats

inferredcites →https://doi.org/10.1152/ajpregu.00534.2014openalex-snapshot

Medial nucleus tractus solitarius oxytocin receptor signaling and food intake control: the role of gastrointestinal satiation signal processing

inferredcites →https://doi.org/10.1152/ajpregu.00604.2003openalex-snapshot

Evidence that paraventricular nucleus oxytocin neurons link hypothalamic leptin action to caudal brain stem nuclei controlling meal size

inferredcites →https://doi.org/10.1152/ajpregu.00781.2002openalex-snapshot

Appetite-inducing accumbens manipulation activates hypothalamic orexin neurons and inhibits POMC neurons

inferredcites →https://doi.org/10.1152/ajpregu.90544.2008openalex-snapshot

Forebrain melanocortin signaling enhances the hindbrain satiety response to CCK-8

inferredcites →https://doi.org/10.1159/000334144openalex-snapshot

Anorexigenic and Orexigenic Hormone Modulation of Mammalian Target of Rapamycin Complex 1 Activity and the Regulation of Hypothalamic Agouti-Related Protein mRNA Expression

inferredcites →https://doi.org/10.1159/000350094openalex-snapshot

Molecular Mechanisms of Depression: Perspectives on New Treatment Strategies

inferredcites →https://doi.org/10.1159/000369072openalex-snapshot

Agouti-Related Protein Neuron Circuits That Regulate Appetite

inferredcites →https://doi.org/10.1172/jci29867openalex-snapshot

Ghrelin modulates the activity and synaptic input organization of midbrain dopamine neurons while promoting appetite

inferredcites →https://doi.org/10.1210/edrv.20.1.0357openalex-snapshot

Interacting Appetite-Regulating Pathways in the Hypothalamic Regulation of Body Weight

inferredcites →https://doi.org/10.1210/en.141.11.4325openalex-snapshot

The Novel Hypothalamic Peptide Ghrelin Stimulates Food Intake and Growth Hormone Secretion

inferredcites →https://doi.org/10.1210/en.141.12.4524openalex-snapshot

The Melanin-Concentrating Hormone Receptor Couples to Multiple G Proteins to Activate Diverse Intracellular Signaling Pathways

inferredcites →https://doi.org/10.1210/en.2008-1479openalex-snapshot

Endogenous Hindbrain Glucagon-Like Peptide-1 Receptor Activation Contributes to the Control of Food Intake by Mediating Gastric Satiation Signaling

inferredcites →https://doi.org/10.1210/en.2011-1443openalex-snapshot

GLP-1 Neurons in the Nucleus of the Solitary Tract Project Directly to the Ventral Tegmental Area and Nucleus Accumbens to Control for Food Intake

inferredcites →https://doi.org/10.1210/en.2014-1986openalex-snapshot

Ventral Tegmental Area Neurotensin Signaling Links the Lateral Hypothalamus to Locomotor Activity and Striatal Dopamine Efflux in Male Mice

inferredcites →https://doi.org/10.1371/journal.pone.0087478openalex-snapshot

Acute High Fat Diet Consumption Activates the Mesolimbic Circuit and Requires Orexin Signaling in a Mouse Model

inferredcites →https://doi.org/10.1371/journal.pone.0119034openalex-snapshot

Activation of the GLP-1 Receptors in the Nucleus of the Solitary Tract Reduces Food Reward Behavior and Targets the Mesolimbic System

inferredcites →https://doi.org/10.1523/jneurosci.1203-05.2006openalex-snapshot

Late-Onset Leanness in Mice with Targeted Ablation of Melanin Concentrating Hormone Neurons

inferredcites →https://doi.org/10.1523/jneurosci.2588-12.2013openalex-snapshot

Hypothalamic Neurotensin Projections Promote Reward by Enhancing Glutamate Transmission in the VTA

inferredcites →https://doi.org/10.1523/jneurosci.3118-09.2010openalex-snapshot

Segregation of Acute Leptin and Insulin Effects in Distinct Populations of Arcuate Proopiomelanocortin Neurons

inferredcites →https://doi.org/10.1523/jneurosci.3187-10.2011openalex-snapshot

Ghrelin Inhibits Visceral Afferent Activation of Catecholamine Neurons in the Solitary Tract Nucleus

inferredcites →https://doi.org/10.1523/jneurosci.3262-11.2011openalex-snapshot

Glucagon-Like Peptide 1 Receptors in Nucleus Accumbens Affect Food Intake

inferredcites →https://doi.org/10.1523/jneurosci.3419-08.2008openalex-snapshot

Oxytocin Enhances Cranial Visceral Afferent Synaptic Transmission to the Solitary Tract Nucleus

inferredcites →https://doi.org/10.1523/jneurosci.3502-07.2007openalex-snapshot

Visceral Afferents Directly Activate Catecholamine Neurons in the Solitary Tract Nucleus

inferredcites →https://doi.org/10.1523/jneurosci.3720-14.2015openalex-snapshot

GABAergic Projections from Lateral Hypothalamus to Paraventricular Hypothalamic Nucleus Promote Feeding

inferredcites →https://doi.org/10.1523/jneurosci.4404-13.2014openalex-snapshot

Ghrelin Acts as an Interface between Physiological State and Phasic Dopamine Signaling

inferredcites →https://doi.org/10.1523/jneurosci.5167-13.2014openalex-snapshot

Leptin Acts via Lateral Hypothalamic Area Neurotensin Neurons to Inhibit Orexin Neurons by Multiple GABA-Independent Mechanisms

inferredcites →https://doi.org/10.1523/jneurosci.5858-09.2010openalex-snapshot

Regulation of Nucleus Accumbens Activity by the Hypothalamic Neuropeptide Melanin-Concentrating Hormone

inferredcites →https://doi.org/10.1523/jneurosci.6326-11.2012openalex-snapshot

The Glucagon-Like Peptide 1 (GLP-1) Analogue, Exendin-4, Decreases the Rewarding Value of Food: A New Role for Mesolimbic GLP-1 Receptors

inferredcites →https://doi.org/10.2337/db06-0730openalex-snapshot

Ghrelin Attenuates the Inhibitory Effects of Glucagon-Like Peptide-1 and Peptide YY(3-36) on Food Intake and Gastric Emptying in Rats

inferredcites →https://doi.org/10.2337/db10-0128openalex-snapshot

Leptin Directly Depolarizes Preproglucagon Neurons in the Nucleus Tractus Solitarius

inferredcites →https://doi.org/10.2337/db11-0489openalex-snapshot

CCK Stimulation of GLP-1 Neurons Involves α1-Adrenoceptor–Mediated Increase in Glutamatergic Synaptic Inputs

inferredcites →https://doi.org/10.2337/diabetes.50.11.2438openalex-snapshot

Chronic Central Infusion of Ghrelin Increases Hypothalamic Neuropeptide Y and Agouti-Related Protein mRNA Levels and Body Weight in Rats

inferredcites →https://doi.org/10.3181/00379727-77-18766openalex-snapshot

Localization of a "Feeding Center" in the Hypothalamus of the Rat

inferredcites →https://doi.org/10.3389/fnsys.2015.00009openalex-snapshot

To ingest or rest? Specialized roles of lateral hypothalamic area neurons in coordinating energy balance

inferredcites →https://doi.org/10.3758/bf03200770openalex-snapshot

The psychobiology of meals

inferredcites →https://doi.org/10.4103/2230-8210.105581openalex-snapshot

PVN pathways controlling energy homeostasis

inferredcites →https://doi.org/10.7554/elife.01462openalex-snapshot

Hypothalamic melanin concentrating hormone neurons communicate the nutrient value of sugar

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.5281/zenodo.23511202zenodo-depositor-declared

inferred← citeshttps://doi.org/10.1002/gch2.202000102openalex-snapshot

Melanins as Sustainable Resources for Advanced Biotechnological Applications

inferred← citeshttps://doi.org/10.1007/978-1-0716-1006-0_749openalex-snapshot

Application of Declarative Programming in Neurobiology

inferred← citeshttps://doi.org/10.1007/978-1-4614-7320-6_749-8openalex-snapshot

Application of Declarative Programming in Neurobiology

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Understanding the layered brain architecture for motivation: Dynamical systems, computational neuroscience, and robotic approaches

inferred← citeshttps://doi.org/10.1016/j.aanat.2022.151886openalex-snapshot

Transcriptomic changes in the hypothalamus of ovariectomized mice: Data from RNA-seq analysis

inferred← citeshttps://doi.org/10.1016/j.cogsys.2020.10.008openalex-snapshot

A bioinspired model of short-term satiety of hunger influenced by food properties in virtual creatures

inferred← citeshttps://doi.org/10.1038/srep40112openalex-snapshot

Hepatic alterations are accompanied by changes to bile acid transporter-expressing neurons in the hypothalamus after traumatic brain injury

inferred← citeshttps://doi.org/10.1080/23262133.2017.1281862openalex-snapshot

Diabetes, adult neurogenesis and brain remodeling: New insights from rodent and zebrafish models

inferred← citeshttps://doi.org/10.1155/2017/6589424openalex-snapshot

Glucose Intake Alters Expression of Neuropeptides Derived from Proopiomelanocortin in the Lateral Hypothalamus and the Nucleus Accumbens in Fructose Preference Rats

inferred← citeshttps://doi.org/10.2174/1573399816666191230111838openalex-snapshot

Is “Leptin Resistance” Another Key Resistance to Manage Type 2 Diabetes?

inferred← citeshttps://doi.org/10.22491/2357-9730.113558openalex-snapshot

Dopamina e comportamento alimentar: polimorfismos em receptores dopaminérgicos e fenótipos relacionados à obesidade

inferred← citeshttps://doi.org/10.4103/nrr.nrr-d-24-00231openalex-snapshot

Single-cell and spatial omics: exploring hypothalamic heterogeneity

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