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Hunger States Switch a Flip-Flop Memory Circuit via a Synaptic AMPK-Dependent Positive Feedback Loop

https://doi.org/10.1016/j.cell.2011.07.039
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What this work says

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

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Expression of ghrelin receptor mRNA in the rat and the mouse brain
inferredcites →https://doi.org/10.1016/0028-3908(77)90019-3openalex-snapshot
Stimulation of food intake by muscimol and beta endorphin
inferredcites →https://doi.org/10.1016/j.bbrc.2007.11.166openalex-snapshot
Ghrelin raises [Ca2+]i via AMPK in hypothalamic arcuate nucleus NPY neurons
inferredcites →https://doi.org/10.1016/j.cmet.2005.05.009openalex-snapshot
Calmodulin-dependent protein kinase kinase-β is an alternative upstream kinase for AMP-activated protein kinase
inferredcites →https://doi.org/10.1016/j.cmet.2005.06.005openalex-snapshot
Ca2+/calmodulin-dependent protein kinase kinase-β acts upstream of AMP-activated protein kinase in mammalian cells
inferredcites →https://doi.org/10.1016/j.cmet.2008.02.011openalex-snapshot
Hypothalamic CaMKK2 Contributes to the Regulation of Energy Balance
inferredcites →https://doi.org/10.1016/j.cmet.2008.03.006openalex-snapshot
Hypothalamic Fatty Acid Metabolism Mediates the Orexigenic Action of Ghrelin
inferredcites →https://doi.org/10.1016/j.neuron.2004.06.004openalex-snapshot
Leptin Receptor Signaling in POMC Neurons Is Required for Normal Body Weight Homeostasis
inferredcites →https://doi.org/10.1016/j.neuron.2008.06.026openalex-snapshot
A Positive Feedback Signal Transduction Loop Determines Timing of Cerebellar Long-Term Depression
inferredcites →https://doi.org/10.1016/j.peptides.2005.01.017openalex-snapshot
NPY-induced feeding: pharmacological characterization using selective opioid antagonists and antisense probes in rats
inferredcites →https://doi.org/10.1016/j.peptides.2006.08.036openalex-snapshot
NPY/AgRP neurons are not essential for feeding responses to glucoprivation
inferredcites →https://doi.org/10.1016/s0006-8993(99)01217-2openalex-snapshot
Identification of neuronal input to the arcuate nucleus (ARH) activated during lactation: implications in the activation of neuropeptide Y neurons
inferredcites →https://doi.org/10.1016/s0022-3565(24)29574-4openalex-snapshot
β-Endorphin-Induced Feeding: Pharmacological Characterization Using Selective Opioid Antagonists and Antisense Probes in Rats
inferredcites →https://doi.org/10.1016/s0896-6273(00)80338-4openalex-snapshot
Heterogeneity of Release Probability, Facilitation, and Depletion at Central Synapses
inferredcites →https://doi.org/10.1016/s0896-6273(01)00190-8openalex-snapshot
Calcium Stores in Hippocampal Synaptic Boutons Mediate Short-Term Plasticity, Store-Operated Ca2+ Entry, and Spontaneous Transmitter Release
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/s0955-0674(02)00314-9openalex-snapshot
Self-perpetuating states in signal transduction: positive feedback, double-negative feedback and bistability
inferredcites →https://doi.org/10.1038/1082openalex-snapshot
Coexpression of Agrp and NPY in fasting-activated hypothalamic neurons
inferredcites →https://doi.org/10.1038/35038090openalex-snapshot
Ghrelin induces adiposity in rodents
inferredcites →https://doi.org/10.1038/35051587openalex-snapshot
A role for ghrelin in the central regulation of feeding
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/nature02440openalex-snapshot
AMP-kinase regulates food intake by responding to hormonal and nutrient signals in the hypothalamus
inferredcites →https://doi.org/10.1038/nature07181openalex-snapshot
UCP2 mediates ghrelin’s action on NPY/AgRP neurons by lowering free radicals
inferredcites →https://doi.org/10.1038/nmeth.1398openalex-snapshot
Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators
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/nn1525openalex-snapshot
Millisecond-timescale, genetically targeted optical control of neural activity
inferredcites →https://doi.org/10.1038/nn1550openalex-snapshot
Topographic mapping of VMH → arcuate nucleus microcircuits and their reorganization by fasting
inferredcites →https://doi.org/10.1074/jbc.m109.026054openalex-snapshot
Generation of Digital Responses in Stress Sensors
inferredcites →https://doi.org/10.1074/jbc.m503824200openalex-snapshot
The Ca2+/Calmodulin-dependent Protein Kinase Kinases Are AMP-activated Protein Kinase Kinases
inferredcites →https://doi.org/10.1074/jbc.m510040200openalex-snapshot
Does AMP-activated Protein Kinase Couple Inhibition of Mitochondrial Oxidative Phosphorylation by Hypoxia to Calcium Signaling in O2-sensing Cells?
inferredcites →https://doi.org/10.1111/j.1432-1033.1995.0558k.xopenalex-snapshot
5-Aminoimidazole-4-Carboxamide Ribonucleoside. A Specific Method for Activating AMP-Activated Protein Kinase in Intact Cells?
inferredcites →https://doi.org/10.1111/j.1469-7793.2000.00769.xopenalex-snapshot
μ‐Opioid receptor inhibits N‐type Ca 2+ channels in the calyx presynaptic terminal of the embryonic chick ciliary ganglion
inferredcites →https://doi.org/10.1113/jphysiol.1952.sp004735openalex-snapshot
Spontaneous subthreshold activity at motor nerve endings
inferredcites →https://doi.org/10.1113/jphysiol.2006.110270openalex-snapshot
Can homeostatic circuits learn and remember?
inferredcites →https://doi.org/10.1119/1.16385openalex-snapshot
The Art of Electronics
inferredcites →https://doi.org/10.1124/jpet.301.2.513openalex-snapshot
Dynorphin A1–17-Induced Feeding: Pharmacological Characterization Using Selective Opioid Antagonists and Antisense Probes in Rats
inferredcites →https://doi.org/10.1126/science.1056602openalex-snapshot
Virus-Assisted Mapping of Neural Inputs to a Feeding Center in the Hypothalamus
inferredcites →https://doi.org/10.1126/science.1089459openalex-snapshot
Rapid Rewiring of Arcuate Nucleus Feeding Circuits by Leptin
inferredcites →https://doi.org/10.1126/science.273.5277.974openalex-snapshot
A Receptor in Pituitary and Hypothalamus That Functions in Growth Hormone Release
inferredcites →https://doi.org/10.1126/science.283.5400.381openalex-snapshot
Emergent Properties of Networks of Biological Signaling Pathways
inferredcites →https://doi.org/10.1126/science.7089556openalex-snapshot
Amplification and Adaptation in Regulatory and Sensory Systems
inferredcites →https://doi.org/10.1152/physrev.1929.9.3.399openalex-snapshot
ORGANIZATION FOR PHYSIOLOGICAL HOMEOSTASIS
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/10.1210/en.2002-221096openalex-snapshot
A Role for the Endogenous Opioid β-Endorphin in Energy Homeostasis
inferredcites →https://doi.org/10.1210/en.2004-0956openalex-snapshot
Transcriptional Regulation of Agouti-Related Protein (Agrp) in Transgenic Mice
inferredcites →https://doi.org/10.1210/en.2004-1397openalex-snapshot
Fasting Induces a Large, Leptin-Dependent Increase in the Intrinsic Action Potential Frequency of Orexigenic Arcuate Nucleus Neuropeptide Y/Agouti-Related Protein Neurons
inferredcites →https://doi.org/10.1210/er.2004-0019openalex-snapshot
Development of Growth Hormone Secretagogues
inferredcites →https://doi.org/10.1210/me.2003-0069openalex-snapshot
High Constitutive Signaling of the Ghrelin Receptor—Identification of a Potent Inverse Agonist
inferredcites →https://doi.org/10.1523/jneurosci.1954-08.2008openalex-snapshot
A FLEX Switch Targets Channelrhodopsin-2 to Multiple Cell Types for Imaging and Long-Range Circuit Mapping
inferredcites →https://doi.org/10.1677/joe.1.06872openalex-snapshot
Differential effects of leptin and refeeding on the fasting-induced decrease of pituitary type 2 deiodinase and thyroid hormone receptor β2 mRNA expression in mice
inferredcites →https://doi.org/10.2307/4615733openalex-snapshot
A Simple Sequentially Rejective Multiple Test Procedure

What points at this work

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

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“Sibling” battle or harmony: crosstalk between nesfatin-1 and ghrelin
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Β-endorphin-immunoreactive perikarya appear to receive innervation from NPY-immunoreactive fiber varicosities in the human hypothalamus
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Leptin
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System Biology of Cell Signaling
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Opposing GPCR signaling programs protein intake setpoint in Drosophila
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Astrocytes Control Food Intake by Inhibiting AGRP Neuron Activity via Adenosine A1 Receptors
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TrpC5 Mediates Acute Leptin and Serotonin Effects via Pomc Neurons
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Activation of AMPK-Regulated CRH Neurons in the PVH is Sufficient and Necessary to Induce Dietary Preference for Carbohydrate over Fat
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Postprandial Hyperglycemia Stimulates Neuroglial Plasticity in Hypothalamic POMC Neurons after a Balanced Meal
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Deficiency of ER Ca2+ sensor STIM1 in AgRP neurons confers protection against dietary obesity
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Hypothalamic steroid receptor coactivator-2 regulates adaptations to fasting and overnutrition
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Melanocortin-3 receptor expression in AgRP neurons is required for normal activation of the neurons in response to energy deficiency
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113338openalex-snapshot
Anti-inflammatory effects of hunger are transmitted to the periphery via projection-specific AgRP circuits
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Opioidergic signaling contributes to food-mediated suppression of AgRP neurons
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AMP-Activated Protein Kinase: A Target for Drugs both Ancient and Modern
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Transmitter Time: Synaptic Plasticity and Metabolic Memory in the Hypothalamus
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AMP-Activated Kinase Links Serotonergic Signaling to Glutamate Release for Regulation of Feeding Behavior in C. elegans
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Rapid versus Delayed Stimulation of Feeding by the Endogenously Released AgRP Neuron Mediators GABA, NPY, and AgRP
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Chronic Activation of γ2 AMPK Induces Obesity and Reduces β Cell Function
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The Homeostatic Force of Ghrelin
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NTS Catecholamine Neurons Mediate Hypoglycemic Hunger via Medial Hypothalamic Feeding Pathways
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AMPK and TOR: The Yin and Yang of Cellular Nutrient Sensing and Growth Control
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A synaptic amplifier of hunger for regaining body weight in the hypothalamus
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Hunger potentiated
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Acute and circadian feedforward regulation of agouti-related peptide hunger neurons
inferred← citeshttps://doi.org/10.1016/j.cnd.2016.09.006openalex-snapshot
Détection cérébrale du glucose, plasticité neuronale et métabolisme énergétique
inferred← citeshttps://doi.org/10.1016/j.cobeha.2015.11.010openalex-snapshot
Integrating adaptive trade-offs between parental care and feeding regulation
inferred← citeshttps://doi.org/10.1016/j.coemr.2022.100337openalex-snapshot
Appetite to learn: An allostatic role for AgRP neurons in the maintenance of energy balance
inferred← citeshttps://doi.org/10.1016/j.conb.2020.05.002openalex-snapshot
Neural circuit mechanisms encoding motivational states in Drosophila
inferred← citeshttps://doi.org/10.1016/j.coph.2017.09.002openalex-snapshot
An appetite for life: brain regulation of hunger and satiety
inferred← citeshttps://doi.org/10.1016/j.cophys.2020.07.007openalex-snapshot
STIM proteins at the intersection of signaling pathways
inferred← citeshttps://doi.org/10.1016/j.cub.2016.05.076openalex-snapshot
Drosophila SLC5A11 Mediates Hunger by Regulating K+ Channel Activity
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174611openalex-snapshot
AgRP/NPY and POMC neurons in the arcuate nucleus and their potential role in treatment of obesity
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2020.108516openalex-snapshot
Short-term high-fat feeding induces a reversible net decrease in synaptic AMPA receptors in the hypothalamus
inferred← citeshttps://doi.org/10.1016/j.mattod.2018.04.006openalex-snapshot
Synthetic biology-inspired design of signal-amplifying materials systems
inferred← citeshttps://doi.org/10.1016/j.mce.2012.06.012openalex-snapshot
AMPK and the neuroendocrine regulation of appetite and energy expenditure
inferred← citeshttps://doi.org/10.1016/j.mce.2014.11.007openalex-snapshot
Cellular energy sensors: AMPK and beyond
inferred← citeshttps://doi.org/10.1016/j.mce.2016.09.028openalex-snapshot
Microglia energy metabolism in metabolic disorder
inferred← citeshttps://doi.org/10.1016/j.mce.2016.12.027openalex-snapshot
Ghrelin modulates gene and protein expression of digestive enzymes in the intestine and hepatopancreas of goldfish (Carassius auratus) via the GHS-R1a: Possible roles of PLC/PKC and AC/PKA intracellular signaling pathways
inferred← citeshttps://doi.org/10.1016/j.molcel.2020.01.020openalex-snapshot
Imprinted Maternally Expressed microRNAs Antagonize Paternally Driven Gene Programs in Neurons
inferred← citeshttps://doi.org/10.1016/j.molmed.2023.10.008openalex-snapshot
RyR-mediated calcium release in hippocampal health and disease
inferred← citeshttps://doi.org/10.1016/j.molmet.2013.02.001openalex-snapshot
Rapid glutamate release in the mediobasal hypothalamus accompanies feeding and is exaggerated by an obesogenic food
inferred← citeshttps://doi.org/10.1016/j.molmet.2013.08.003openalex-snapshot
The hormonal signature of energy deficit: Increasing the value of food reward
inferred← citeshttps://doi.org/10.1016/j.molmet.2013.10.001openalex-snapshot
Arcuate AgRP neurons mediate orexigenic and glucoregulatory actions of ghrelin
inferred← citeshttps://doi.org/10.1016/j.molmet.2014.05.006openalex-snapshot
The histone acetyltransferase MOF activates hypothalamic polysialylation to prevent diet-induced obesity in mice
inferred← citeshttps://doi.org/10.1016/j.molmet.2016.01.003openalex-snapshot
Postnatal undernutrition delays a key step in the maturation of hypothalamic feeding circuits
inferred← citeshttps://doi.org/10.1016/j.molmet.2016.08.007openalex-snapshot
Adiponectin potentiates the acute effects of leptin in arcuate Pomc neurons
inferred← citeshttps://doi.org/10.1016/j.molmet.2018.08.011openalex-snapshot
Cellular and synaptic reorganization of arcuate NPY/AgRP and POMC neurons after exercise
inferred← citeshttps://doi.org/10.1016/j.molmet.2019.11.014openalex-snapshot
Fasting induces remodeling of the orexigenic projections from the arcuate nucleus to the hypothalamic paraventricular nucleus, in a growth hormone secretagogue receptor–dependent manner
inferred← citeshttps://doi.org/10.1016/j.molmet.2024.101975openalex-snapshot
Hypothalamic AgRP neurons regulate the hyperphagia of lactation
inferred← citeshttps://doi.org/10.1016/j.molmet.2025.102178openalex-snapshot
VGluT3 BNST neurons transmit GABA and restrict sucrose consumption
inferred← citeshttps://doi.org/10.1016/j.molmet.2025.102209openalex-snapshot
Fructose-induced synaptic and neuronal adaptations at neuropeptide Y/agouti-related peptide neurons
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2016.03.032openalex-snapshot
Driving the need to feed: Insight into the collaborative interaction between ghrelin and endocannabinoid systems in modulating brain reward systems
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2016.12.010openalex-snapshot
The neurological effects of ghrelin in brain diseases: Beyond metabolic functions
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2021.02.021openalex-snapshot
Motivational competition and the paraventricular thalamus
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2021.06.034openalex-snapshot
Neural mechanisms underlying the role of fructose in overfeeding
inferred← citeshttps://doi.org/10.1016/j.neulet.2021.136362openalex-snapshot
Comparison of the effects of intracerebroventricular administration of glucagon-like peptides 1 and 2 on hypothalamic appetite regulating factors and sleep-like behavior in chicks
inferred← citeshttps://doi.org/10.1016/j.neures.2022.11.006openalex-snapshot
Mechanistic insights on impact of Adenosine monophosphate-activated protein kinase (AMPK) mediated signalling pathways on cerebral ischemic injury
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.09.033openalex-snapshot
Imaging hypothalamic activity using diffusion weighted magnetic resonance imaging in the mouse and human brain
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.11.027openalex-snapshot
Fasting Activation of AgRP Neurons Requires NMDA Receptors and Involves Spinogenesis and Increased Excitatory Tone
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.08.035openalex-snapshot
Peptide Neuromodulation in Invertebrate Model Systems
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.09.014openalex-snapshot
Neuropeptide Transmission in Brain Circuits
inferred← citeshttps://doi.org/10.1016/j.neuron.2013.02.018openalex-snapshot
Hypothalamic Survival Circuits: Blueprints for Purposive Behaviors
inferred← citeshttps://doi.org/10.1016/j.neuron.2016.05.025openalex-snapshot
A Postsynaptic AMPK→p21-Activated Kinase Pathway Drives Fasting-Induced Synaptic Plasticity in AgRP Neurons
inferred← citeshttps://doi.org/10.1016/j.neuron.2017.06.014openalex-snapshot
Toward a Wiring Diagram Understanding of Appetite Control
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2019.02.021openalex-snapshot
Extracellular glucose-dependent IPSC enhancement by leptin in fast-spiking to pyramidal neuron connections via JAK2-PI3K pathway in the rat insular cortex
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2026.111116openalex-snapshot
Metformin enhances hippocampal excitatory synaptic transmission and preserves synaptic plasticity under amyloid-β oligomer-induced dysfunction
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2012.07.010openalex-snapshot
Opioids inhibit visceral afferent activation of catecholamine neurons in the solitary tract nucleus
inferred← citeshttps://doi.org/10.1016/j.npep.2015.08.008openalex-snapshot
Fasted/fed states regulate postsynaptic hub protein DYNLL2 and glutamatergic transmission in oxytocin neurons in the hypothalamic paraventricular nucleus
inferred← citeshttps://doi.org/10.1016/j.npep.2018.11.005openalex-snapshot
The effect of ghrelin and adenosine mono phosphate kinase (AMPK) on the passive avoidance memory in male wistar rats
inferred← citeshttps://doi.org/10.1016/j.pbb.2019.06.001openalex-snapshot
Behavioral cross-sensitization between cocaine and ethanol is accompanied by parallel changes in the activity of AMPK system
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2017.03.014openalex-snapshot
Estradiol effects on hypothalamic AMPK and BAT thermogenesis: A gateway for obesity treatment?
inferred← citeshttps://doi.org/10.1016/j.phrs.2026.108334openalex-snapshot
Loss of ETV4 triggers PPM1E downregulation and AMPK–ULK1-dependent autophagy to promote intrinsic trametinib resistance in breast cancer
inferred← citeshttps://doi.org/10.1016/j.physbeh.2013.03.030openalex-snapshot
Differential effects of central ghrelin on fatty acid metabolism in hypothalamic ventral medial and arcuate nuclei
inferred← citeshttps://doi.org/10.1016/j.physbeh.2020.113039openalex-snapshot
Effects of metabolic state on the regulation of melanocortin circuits
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2016.03.001openalex-snapshot
The role of astrocytes in the hypothalamic response and adaptation to metabolic signals
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2021.105143openalex-snapshot
Weight gain and neuroadaptations elicited by high fat diet depend on fatty acid composition
inferred← citeshttps://doi.org/10.1016/j.reach.2019.100032openalex-snapshot
Neuropeptide Y – Its role in human performance and extreme environments
inferred← citeshttps://doi.org/10.1016/j.reprotox.2023.108471openalex-snapshot
Maternal chronic caffeine intake impairs fertility, placental vascularization and fetal development in mice
inferred← citeshttps://doi.org/10.1016/j.steroids.2019.108428openalex-snapshot
Membrane and nuclear initiated estrogenic regulation of homeostasis
inferred← citeshttps://doi.org/10.1016/j.tem.2012.10.005openalex-snapshot
Metabolic transceivers: in tune with the central melanocortin system
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2016.08.004openalex-snapshot
The effects of late gestation maternal nutrient restriction with or without protein supplementation on endocrine regulation of newborn and postnatal beef calves
inferred← citeshttps://doi.org/10.1016/j.tige.2020.03.007openalex-snapshot
Food intake regulation: Relevance to bariatric and metabolic endoscopic therapies
inferred← citeshttps://doi.org/10.1016/j.tins.2012.12.005openalex-snapshot
Hypothalamic control of energy balance: insights into the role of synaptic plasticity
inferred← citeshttps://doi.org/10.1016/j.tins.2013.05.003openalex-snapshot
Neuronal circuits that regulate feeding behavior and metabolism
inferred← citeshttps://doi.org/10.1016/j.tins.2013.07.003openalex-snapshot
Towards a ‘systems’-level understanding of the nervous system and its disorders
inferred← citeshttps://doi.org/10.1016/j.tins.2016.12.003openalex-snapshot
Current Understanding of the Hypothalamic Ghrelin Pathways Inducing Appetite and Adiposity
inferred← citeshttps://doi.org/10.1016/j.tips.2022.04.007openalex-snapshot
Hypothalamic AMPK as a possible target for energy balance-related diseases
inferred← citeshttps://doi.org/10.1016/j.yfrne.2012.08.002openalex-snapshot
Anterior pituitary cell networks
inferred← citeshttps://doi.org/10.1016/j.yfrne.2012.09.002openalex-snapshot
Many mouths to feed: The control of food intake during lactation
inferred← citeshttps://doi.org/10.1017/s002966511200078xopenalex-snapshot
Hypothalamic dysfunction in obesity
inferred← citeshttps://doi.org/10.1038/aps.2013.150openalex-snapshot
Optogenetics and synaptic plasticity
inferred← citeshttps://doi.org/10.1038/embor.2013.177openalex-snapshot
Complex diseases require complex therapies
inferred← citeshttps://doi.org/10.1038/mp.2014.30openalex-snapshot
Molecular and cellular regulation of hypothalamic melanocortin neurons controlling food intake and energy metabolism
inferred← citeshttps://doi.org/10.1038/nature11270openalex-snapshot
Deconstruction of a neural circuit for hunger
inferred← citeshttps://doi.org/10.1038/nature12956openalex-snapshot
An excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger
inferred← citeshttps://doi.org/10.1038/nature14177openalex-snapshot
Genetic studies of body mass index yield new insights for obesity biology
inferred← citeshttps://doi.org/10.1038/nature14260openalex-snapshot
Hypothalamic POMC neurons promote cannabinoid-induced feeding
inferred← citeshttps://doi.org/10.1038/nature14416openalex-snapshot
Neurons for hunger and thirst transmit a negative-valence teaching signal
inferred← citeshttps://doi.org/10.1038/ncomms7618openalex-snapshot
Interplay between glucose and leptin signalling determines the strength of GABAergic synapses at POMC neurons
inferred← citeshttps://doi.org/10.1038/nn.3219openalex-snapshot
Synaptic plasticity in neuronal circuits regulating energy balance
inferred← citeshttps://doi.org/10.1038/nn.3374openalex-snapshot
Glucocorticoid feedback uncovers retrograde opioid signaling at hypothalamic synapses
inferred← citeshttps://doi.org/10.1038/nn.3725openalex-snapshot
Leptin signaling in astrocytes regulates hypothalamic neuronal circuits and feeding
inferred← citeshttps://doi.org/10.1038/nn.4091openalex-snapshot
Optogenetics: 10 years of microbial opsins in neuroscience
inferred← citeshttps://doi.org/10.1038/nn.4202openalex-snapshot
Melanocortin-4 receptor–regulated energy homeostasis
inferred← citeshttps://doi.org/10.1038/nrd3739openalex-snapshot
Limitations in anti-obesity drug development: the critical role of hunger-promoting neurons
inferred← citeshttps://doi.org/10.1038/nrendo.2013.256openalex-snapshot
Metformin—mode of action and clinical implications for diabetes and cancer
inferred← citeshttps://doi.org/10.1038/nrendo.2016.222openalex-snapshot
The cellular and molecular bases of leptin and ghrelin resistance in obesity
inferred← citeshttps://doi.org/10.1038/nrendo.2016.67openalex-snapshot
Hypothalamic AMPK: a canonical regulator of whole-body energy balance
inferred← citeshttps://doi.org/10.1038/nrendo.2017.78openalex-snapshot
FGF1 — a new weapon to control type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.1038/nrm.2017.95openalex-snapshot
AMPK: guardian of metabolism and mitochondrial homeostasis
inferred← citeshttps://doi.org/10.1038/nrm3311openalex-snapshot
AMPK: a nutrient and energy sensor that maintains energy homeostasis
inferred← citeshttps://doi.org/10.1038/s12276-022-00758-4openalex-snapshot
Brain circuits for promoting homeostatic and non-homeostatic appetites
inferred← citeshttps://doi.org/10.1038/s41366-023-01265-wopenalex-snapshot
High sucrose consumption decouples intrinsic and synaptic excitability of AgRP neurons without altering body weight
inferred← citeshttps://doi.org/10.1038/s41366-025-01898-zopenalex-snapshot
Integrating genetic and transcriptomic data to identify genes underlying obesity risk loci
inferred← citeshttps://doi.org/10.1038/s41378-019-0061-6openalex-snapshot
Inductively coupled, mm-sized, single channel optical neuro-stimulator with intensity enhancer
inferred← citeshttps://doi.org/10.1038/s41380-019-0506-1openalex-snapshot
A POMC-originated circuit regulates stress-induced hypophagia, depression, and anhedonia
inferred← citeshttps://doi.org/10.1038/s41380-020-00908-yopenalex-snapshot
ADORA1-driven brain-sympathetic neuro-adipose connections control body weight and adipose lipid metabolism
inferred← citeshttps://doi.org/10.1038/s41380-023-02283-wopenalex-snapshot
Anxiolytic effect of antidiabetic metformin is mediated by AMPK activation in mPFC inhibitory neurons
inferred← citeshttps://doi.org/10.1038/s41398-018-0167-xopenalex-snapshot
Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet
inferred← citeshttps://doi.org/10.1038/s41398-018-0260-1openalex-snapshot
Fasting enhances extinction retention and prevents the return of fear in humans
inferred← citeshttps://doi.org/10.1038/s41398-019-0438-1openalex-snapshot
AGRP neurons modulate fasting-induced anxiolytic effects
inferred← citeshttps://doi.org/10.1038/s41398-020-01161-1openalex-snapshot
AgRP neurons trigger long-term potentiation and facilitate food seeking
inferred← citeshttps://doi.org/10.1038/s41421-025-00857-2openalex-snapshot
Prefrontal cortex-to-hypothalamic outputs orchestrate cue-potentiated palatable food consumption via AMPKβ2 signaling
inferred← citeshttps://doi.org/10.1038/s41467-018-05721-4openalex-snapshot
Loss of the E3 ubiquitin ligase MKRN1 represses diet-induced metabolic syndrome through AMPK activation
inferred← citeshttps://doi.org/10.1038/s41467-020-20050-1openalex-snapshot
Estrogen-sensitive medial preoptic area neurons coordinate torpor in mice
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