Neurobiology of Feeding and Energy Expenditure

Positional cloning of the mouse obese gene and its human homologue

Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., & Friedman, J. M. (1994) · Nature · doi:10.1038/372425a0 · Cited by 13,419

Ghrelin is a growth-hormone-releasing acylated peptide from stomach

Kojima, M., Hosoda, H., Date, Y., Nakazato, M., Matsuo, H., & Kangawa, K. (1999) · Nature · doi:10.1038/45230 · Cited by 8,479

Orexins and orexin receptors: a family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior

Sakurai, T., Amemiya, A., Ishii, M., Matsuzaki, I., Chemelli, R. M., Tanaka, H., Williams, S. C., Richardson, J. A., Kozlowski, G. P., Wilson, S., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)80949-6 · Cited by 5,501

LTP and LTD

Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968

Ghrelin induces adiposity in rodents

Tschöp, M., Smiley, D. L., & Heiman, M. L. (2000) · Nature · doi:10.1038/35038090 · Cited by 3,949

Identification and expression cloning of a leptin receptor, OB-R.

Tartaglia, L. A., Dembski, M., Weng, X., Deng, N., Culpepper, J., Devos, R., Richards, G. J., Campfield, L. A., Clark, F. T., Deeds, J., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90151-5 · Cited by 3,496

Neurons containing hypocretin (orexin) project to multiple neuronal systems

Peyron, C., Tighe, D. K., van den Pol, A. N., de Lecea, L., Heller, H. C., Sutcliffe, J. G., & Kilduff, T. S. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-23-09996.1998 · Cited by 3,466

Narcolepsy in orexin Knockout Mice

Chemelli, R. M., Willie, J. T., Sinton, C. M., Elmquist, J. K., Scammell, T., Lee, C., Richardson, J. A., Williams, S. C., Xiong, Y., Kisanuki, Y., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)81973-x · Cited by 3,095

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

Cowley, M. A., Smart, J. L., Rubinstein, M., Cerdán, M. G., Diano, S., Horvath, T. L., Cone, R. D., & Low, M. J. (2001) · Nature · doi:10.1038/35078085 · Cited by 2,356

Evidence That the Diabetes Gene Encodes the Leptin Receptor: Identification of a Mutation in the Leptin Receptor Gene in db/db Mice

Chen, H., Charlat, O., Tartaglia, L. A., Woolf, E. A., Weng, X., Ellis, S. J., Lakey, N. D., Culpepper, J., More, K. J., Breitbart, R. E., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)81294-5 · Cited by 2,214

Early overnutrition alters synaptic signaling and induces leptin resistance in arcuate proopiomelanocortin neurons

Roberts, B. L., Bennett, C. M., Carroll, J. M., Lindsley, S. R., & Kievit, P. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.04.002 · Cited by 18

Decreased rates of operant food self-administration are associated with reward deficits in high-fat feeding mice

Íbias, J., Miguéns, M., Rio, D. D., Valladolid‐Acebes, I., Stucchi, P., Ambrosio, E., Martín, M. E., Morales, L., Ruiz‐Gayo, M., & Olmo, N. D. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-0980-4 · Cited by 19

Effects of Neonatal Programming on Hypothalamic Mechanisms Controlling Energy Balance

Contreras, C., Novelle, M. G., Leis, R., Diéguez, C., Skrede, S., & López, M. (2013) · Hormone and Metabolic Research · doi:10.1055/s-0033-1351281 · Cited by 18

Effect of residual feed intake on hypothalamic gene expression and meat quality in Angus-sired cattle grown during the hot season1,2

Perkins, S. D., Key, C. N., Marvin, M. N., Garrett, C. F., Foradori, C. D., Bratcher, C. L., Kriese-Anderson, L. A., & Brandebourg, T. D. (2014) · Journal of Animal Science · doi:10.2527/jas.2013-7020 · Cited by 18

Influence of MCHR2 and MCHR2-AS1 Genetic Polymorphisms on Body Mass Index in Psychiatric Patients and In Population-Based Subjects with Present or Past Atypical Depression

Delacrétaz, A., Preisig, M., Vandenberghe, F., Saigí-Morgui, N., Quteineh, L., Choong, E., Gholam‐Rezaee, M., Kutalik, Z., Magistretti, P. J., Aubry, J., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0139155 · Cited by 18

Autonomic neuropathy in experimental models of diabetes mellitus

Schmidt, R. E. (2014) · Handbook of clinical neurology · doi:10.1016/b978-0-444-53480-4.00038-2 · Cited by 16

Tryptophan metabolic pathway plays a key role in the stress-induced emotional eating

Zhu, Y., Yin, L., Liu, Q., Guan, Y., Nie, S., Zhu, Y., & Mo, F. (2024) · Current Research in Food Science · doi:10.1016/j.crfs.2024.100754 · Cited by 20

Vitamin A supplementation at pharmacological doses induces nitrosative stress on the hypothalamus of adult Wistar rats

de Oliveira, M. R., Oliveira, M. W. S., da Rocha, R. F., & Moreira, J. C. F. (2009) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2009.02.006 · Cited by 17

Preference for high-fat diet is developed by young Swiss CD1 mice after short-term feeding and is prevented by NMDA receptor antagonists

Buttigieg, A., Flores, O., Hernández, A., Sáez‐Briones, P., Burgos, H., & Morgan, C. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.10.018 · Cited by 16

Interacting Neural Processes of Feeding, Hyperactivity, Stress, Reward, and the Utility of the Activity-Based Anorexia Model of Anorexia Nervosa

Ross, R., Mandelblat-Cerf, Y., & Verstegen, A. M. J. (2016) · Harvard Review of Psychiatry · doi:10.1097/hrp.0000000000000111 · Cited by 15

Zinc Finger Transcription Factor Zbtb16 Coordinates the Response to Energy Deficit in the Mouse Hypothalamus

Cheng, H., Pablico, S. J., Lee, J., Chang, J. S., & Yu, S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.592947 · Cited by 14

Effects of Estradiol on Cerebrospinal Fluid Levels of Agouti-Related Protein in Ovariectomized Rhesus Monkeys

Xiao, E., Kim, A. J., Dutia, R., Conwell, I. M., Ferin, M., & Wardlaw, S. L. (2010) · Endocrinology · doi:10.1210/en.2009-0853 · Cited by 15

Visualizing hormone actions in the brain

Brabant, G. E., Cain, J. R., Jackson, A., & Kreitschmann‐Andermahr, I. (2011) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2011.01.004 · Cited by 14

Enhanced motivation for food reward induced by stress and attenuation by corticotrophin-releasing factor receptor antagonism in rats: implications for overeating and obesity

Liu, X. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3838-1 · Cited by 15

Study and research of feeding behavior: Roots, development and challenges / Estudio e investigación del comportamiento alimentario: Raíces, desarrollo y retos

López-Espinoza, A., Moreno, A. G. M., Cervantes, V. G. A., Estrada, J. G. S., Navarro-Meza, M., Reyes-Castillo, Z., García-Sánchez, N. E., & Jiménez-Briseño, A. (2018) · Revista Mexicana de Trastornos Alimentarios/Mexican Journal of Eating Disorders · doi:10.22201/fesi.20071523e.2018.1.465 · Cited by 15

The effect of chronic immobilization stress on leptin signaling in the ovariectomized (OVX) rat

Larco, D. O., Cruthirds, D. F., Weiser, M. J., Handa, R. J., & Wu, T. J. (2012) · Endocrine · doi:10.1007/s12020-012-9716-x · Cited by 15

The Transition Zone Protein AHI1 Regulates Neuronal Ciliary Trafficking of MCHR1 and Its Downstream Signaling Pathway

Hsiao, Y.-C., Muñoz‐Estrada, J., Tuz, K., & Ferland, R. J. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2993-20.2021 · Cited by 14

Rolling out physical exercise and energy homeostasis: Focus on hypothalamic circuitries

Cavalcanti‐de‐Albuquerque, J. P., & Donato, J. (2021) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2021.100944 · Cited by 16

Energy Homeostasis: Paraventricular Nucleus (PVN) System

Richard, D., & Timofeeva, E. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00453-8 · Cited by 14

Cloning, distribution, and effects of growth regulation of MC3R and MC4R in red crucian carp (Carassius auratus red var.)

Huang, L., Deng, X., Yang, X., Tang, Z., Fan, S., Zhou, Z., Tao, M., & Liu, S. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1310000 · Cited by 13

Decreased food anticipatory activity of obese mice relates to hypothalamic c-Fos expression

Luna‐Illades, C., Morales, T., & Miranda‐Anaya, M. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.05.020 · Cited by 13

Effects of bariatric surgery on the central nervous system and eating behavior in humans: a systematic review on the neuroimaging studies

Tonelli, H. A., Sartori, F. M., Marchesini, J. C., Marchesini, J. B., & Tonelli, D. G. (2013) · Jornal Brasileiro de Psiquiatria · doi:10.1590/s0047-20852013000400007 · Cited by 12

MAPK Erk5 in Leptin Receptor‒Expressing Neurons Controls Body Weight and Systemic Energy Homeostasis in Female Mice

Horie, T., Park, G., Inaba, Y., Hashiuchi, E., Iezaki, T., Tokumura, K., Fukasawa, K., Yamada, T., Hiraiwa, M., Kitaguchi, Y., et al. (2019) · Endocrinology · doi:10.1210/en.2019-00090 · Cited by 12

Understanding the control of ingestive behavior in primates

Wilson, M. E., Moore, C. J., Ethun, K. F., & Johnson, Z. P. (2014) · Hormones and Behavior · doi:10.1016/j.yhbeh.2014.04.005 · Cited by 13

Hypothalamic neural circuits regulating energy expenditure

Basu, R., & Flak, J. N. (2024) · Vitamins and hormones · doi:10.1016/bs.vh.2024.07.004 · Cited by 12

Energy Homeostasis: Paraventricular Nucleus System☆

Timofeeva, E., Caron, A., & Richard, D. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.02753-x · Cited by 11

Divergent and convergent roles for insulin-like peptides in the worm, fly and mammalian nervous systems

Lau, H. E., & Chalasani, S. H. (2014) · Invertebrate Neuroscience · doi:10.1007/s10158-013-0166-9 · Cited by 11

Short-term high-fat feeding induces a reversible net decrease in synaptic AMPA receptors in the hypothalamus

Liu, J., Dimitrov, S., Sawangjit, A., Jan Born, A., Ehrlich, I., & Hallschmid, M. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2020.108516 · Cited by 11

Ontogeny of energy homeostatic pathways via neuroendocrine signaling in Atlantic salmon

Moen, A. G., Murashita, K., & Finn, R. N. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20803 · Cited by 11

Differential expression of appetite‐regulating genes in avian models of anorexia and obesity

Yi, J., Yuan, J., Gilbert, E. R., Siegel, P. B., & Cline, M. A. (2017) · Journal of Neuroendocrinology · doi:10.1111/jne.12510 · Cited by 10

Extrahypothalamic Control of Energy Balance and Its Connection with Reproduction: Roles of the Amygdala

Pineda, R., Torres, E., & Tena‐Sempere, M. (2021) · Metabolites · doi:10.3390/metabo11120837 · Cited by 10

Perinatal exposure to tributyltin affects feeding behavior and expression of hypothalamic neuropeptide Y in the paraventricular nucleus of adult mice

Ponti, G., Bo, E., Bonaldo, B., Farinetti, A., Marraudino, M., Panzica, G., & Gotti, S. (2022) · Journal of Anatomy · doi:10.1111/joa.13766 · Cited by 9

Peripheral 5-HT Mediates Gonadotropin-Inhibitory Hormone-Induced Feeding Behavior and Energy Metabolism Disorder in Chickens via the 5-HT2C Receptor

Song, X., Xu, W., Li, Z., Zhang, X., Liu, C., Han, K., Chen, L., Shi, Y., Xu, C., Han, D., et al. (2024) · Neuroendocrinology · doi:10.1159/000539238 · Cited by 9

A normative framework dissociates need and motivation in hypothalamic neurons

Kim, K. S., Lee, Y. H., Kim, Y., Yun, J. W., Song, H. Y., Park, J. S., Jung, S.-H., Sohn, J., Kim, K. W., Kim, H. R., et al. (2024) · Science Advances · doi:10.1126/sciadv.ado1820 · Cited by 9

Loss of the centrosomal protein Cenpj leads to dysfunction of the hypothalamus and obesity in mice

Ding, W., Zhang, C., Wang, B., Zhou, X., Sun, L., Zhong, S., Liu, J., Zhang, J., Wang, X., & Wu, Q. (2020) · Science China Life Sciences · doi:10.1007/s11427-020-1767-5 · Cited by 12

Voluntary food intake of pregnant and non-pregnant red deer hinds

Scott, I., Asher, G. W., Barrell, G. K., & Juan, J. V. (2013) · Livestock Science · doi:10.1016/j.livsci.2013.04.021 · Cited by 9

Neurobiology of food choices—between energy homeostasis, reward system, and neuroeconomics

Enax, L., & Weber, B. (2016) · e-Neuroforum · doi:10.1007/s13295-015-0020-0 · Cited by 10

Leptin coordinates efferent sympathetic outflow to the white adipose tissue through the midbrain centrally-projecting Edinger-Westphal nucleus in male rats

Xu, L., Füredi, N., Lutter, C., Geenen, B., Pétervári, E., Balaskó, M., Dénes, Á., Kovács, K., Gaszner, B., & Kozicz, T. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108898 · Cited by 9

Functional Organization of the Brain

Fountoulakis, K. N. (2022) · Springer eBooks · doi:10.1007/978-3-031-10351-3_10 · Cited by 9

Expression changes of hypothalamic Ahi1 in mice brain: implication in sensing insulin signaling

Niu, S., Wang, H., Huang, Z., Rao, X., Cai, X., Liang, T., Xu, J., Xu, X., & Sheng, G. (2012) · Molecular Biology Reports · doi:10.1007/s11033-012-1834-2 · Cited by 8

A temperature hypothesis of hypothalamus-driven obesity.

Horváth, T. L., Stachenfeld, N. S., & Diano, S. (2014) · Europe PMC (PubMed Central) · Cited by 8

Combined brain Fe, Cu, Zn and neurometabolite analysis – a new methodology for unraveling the efficacy of transcranial direct current stimulation (tDCS) in appetite control

Ziomber, A., Surówka, A. D., Antkiewicz‐Michaluk, L., Romańska, I., Wróbel, P., & Szczerbowska‐Boruchowska, M. (2018) · Metallomics · doi:10.1039/c7mt00329c · Cited by 8

Nutritionally induced tanycytic plasticity in the hypothalamus of adult ewes

Prezotto, L. D., Thorson, J. F., Prévot, V., Redmer, D. A., & Grazul‐Bilska, A. T. (2020) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2020.106438 · Cited by 8

Procalcitonin N-Terminal Peptide Causes Catabolic Effects via the Hypothalamus and Prostaglandin-Dependent Pathways

Tavares, E., & Miñano, F. J. (2008) · Neuroendocrinology · doi:10.1159/000155137 · Cited by 8

Obesity and obesity related disease in adulthood: the dark side of early life exposure to Environmental Chemical Disruptors

Lorenzo, M. D., Aurino, L., Lonardo, M. S., Cacciapuoti, N., Nasti, G., Belfiore, A., Guida, B., & Chiurazzi, M. (2025) · Journal of Endocrinological Investigation · doi:10.1007/s40618-025-02620-6 · Cited by 7

3.01 – Membrane-Initiated Effects of Estradiol in the Central Nervous System

Rønnekleiv, O., & Kelly, M. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803592-4.00043-2 · Cited by 4

daf-16/FOXO isoform b in AIY neurons is involved in low preference for Bifidobacterium infantis in Caenorhabditis elegans

Sun, S., Ohta, A., Kuhara, A., Nishikawa, Y., & Kage‐Nakadai, E. (2019) · Neuroscience Research · doi:10.1016/j.neures.2019.01.011 · Cited by 7

Parallel Paths in PVH Control of Feeding

Varela, L., & Horváth, T. L. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.026 · Cited by 7

Human hypothalamus shows differential responses to basic motivational stimuli—an invasive electrophysiology study

Nager, W., Krauss, J. K., Heldmann, M., Marco‐Pallarés, J., Capelle, H., Lütjens, G., Bolat, S., Dengler, R., & Münte, T. F. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.05.019 · Cited by 7

Gonadotropin-Releasing Hormone Fibers Contact POMC Neurons in the Hypothalamic Arcuate Nucleus

Sótonyi, P., Mezei, G., Rácz, B., Dallman, M. F., Abizaid, A. B., & Horváth, T. L. (2010) · Reproductive Sciences · doi:10.1177/1933719110378346 · Cited by 7

Cell-Nonautonomous Control of the UPR: Mastering Energy Homeostasis

Mardones, P., Dillin, A. G., & Hetz, C. A. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.07.009 · Cited by 7

Mediobasal Hypothalamic Neurons Contribute to the Control of Brown Adipose Tissue Sympathetic Nerve Activity and Cutaneous Vasoconstriction

Mota, C. M. D., & Madden, C. J. (2023) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2023.103551 · Cited by 6

The Diverse Network of Brain Histamine in Feeding: Dissect its Functions in a Circuit-Specific Way

Xu, L., Lin, W., Zheng, Y., Wang, Y., & Chen, Z. (2022) · Current Neuropharmacology · doi:10.2174/1570159x21666221117153755 · Cited by 8

The role of Gα protein signaling in the membrane estrogen receptor-mediated signaling

Zheng, S., Wu, L., Fan, C., Lin, J., Zhang, Y., Simoncini, T., & Fu, X. (2020) · Gynecological Endocrinology · doi:10.1080/09513590.2020.1851674 · Cited by 6

Neurosecretory protein GL in GIFT tilapia (Oreochromis niloticus): cDNA cloning, tissue distribution and effects of feeding on its expression

Huang, J., Hao, Y., Lai, K., Lyu, L., Yuan, X., Yang, G., Li, W., & Sun, C. (2022) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2022.114096 · Cited by 5

Minor differences in the molecular machinery mediating regulated membrane fusion has major impact on metabolic health

Valladolid‐Acebes, I., Daraio, T., Brismar, K., Hökfelt, T. G. M., & Bark, C. (2016) · Adipocyte · doi:10.1080/21623945.2015.1137689 · Cited by 6

L’expérience sensorielle et nutritionnelle des parents et leur état métabolique orientent le comportement alimentaire de leur descendance

Parnet, P., Paillé, V., Jimenez, F. B., Kaeffer, B., Schaal, B., Bouret, S. G., & Amarger, V. (2016) · médecine/sciences · doi:10.1051/medsci/20163201014 · Cited by 5

Ventral Tegmental Area Microinjected-SKF38393 Increases Regular Chow Intake in 18 Hours Food-Deprived Rats

Rad, F. S., Haghparast, A., & Eliassi, A. (2020) · Basic and Clinical Neuroscience Journal · doi:10.32598/bcn.11.6.2226.1 · Cited by 5

Seasonal and Nutritional Fluctuations in the mRNA Levels of the Short Form of the Leptin Receptor (LRa) in the Hypothalamus and Anterior Pituitary in Resistin-Treated Sheep

Biernat, W., Szczęsna, M., Kirsz, K., & Zieba, D. A. (2021) · Animals · doi:10.3390/ani11082451 · Cited by 5

A Sympathetic View on Free Radicals in Diabetes

Diano, S., & Horváth, T. L. (2010) · Neuron · doi:10.1016/j.neuron.2010.06.011 · Cited by 5

Firing Up Brown Fat with Brain Amylin

López, M., & Nogueiras, R. (2013) · Endocrinology · doi:10.1210/en.2013-1445 · Cited by 4

Food reward derives from nutrient content and sensory qualities

Stuphorn, V. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2109735118 · Cited by 3

Disruption of CRTC1 and CRTC2 in Sim1 cells strongly increases high-fat diet intake in female mice but has a modest impact on male mice

Tanaka, J., Ishikawa, F., Jinno, T., Miyakita, M., Miyamori, H., Sasaki, T., Yokokawa, T., Goto, T., Inoue, K., & Matsumura, S. (2022) · PLoS ONE · doi:10.1371/journal.pone.0262577 · Cited by 3

The Pleasures and Pains of Brain Regulatory Systems for Eating

Panksepp, J. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374387-9.00001-5 · Cited by 3

Combining Quantitative Food-intake Assays and Forcibly Activating Neurons to Study Appetite in Drosophila

Jiang, L., Zhan, Y., & Zhu, Y. (2018) · Journal of Visualized Experiments · doi:10.3791/56900 · Cited by 3

Functional and Anatomical Dissection of Feeding Circuits

Atasoy, D., & Sternson, S. M. (2016) · Wiley eBooks · doi:10.1002/9781118839317.ch6 · Cited by 4

Acute Exercise Effects on Appetite and Energy Intake in People Living With Overweight and Obesity: A Systematic Review and Meta-Analysis

Li, N., Wu, M., & Li, Y. (2025) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2025-0078 · Cited by 2

Cardiometabolic Risk, Inflammation, and Neurodegenerative Disorders

Palavra, F., Ciampi, E., & Sena, A. (2015) · Springer eBooks · doi:10.1007/978-3-319-16018-4_7 · Cited by 2

Too Fat to Fly? New Brain Circuits Regulate Obesity in Drosophila

Kaun, K. R., & Heberlein, U. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.023 · Cited by 2

RIPping off GABA Release in Hypothalamic Circuits Causes Obesity

Bouret, S. G. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.10.014 · Cited by 2

Basic Vital Functions and Instincts

Ferentinos, P. P., Kokras, N., & Konstantakopoulos, G. (2019) · Springer eBooks · doi:10.1007/978-3-030-18323-3_3 · Cited by 2

Mechanisms of Homeostatically Regulated Behaviors

Elmquist, J. K., Zigman, J. M., & Saper, C. B. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_62 · Cited by 2

Neural Systems of Motivation

Cardinal, R. N., & Everitt, B. J. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-045396-5.00167-6 · Cited by 2

Insulin signalling activates multiple feedback loops to elicit hunger-induced feeding in DrosophilaPreprint

Sudhakar, S. R., & Varghese, J. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/364554 · Cited by 2

CRISPR Knockdown of Kcnq3 Attenuates the M-current in NPY/AgRP NeuronsPreprint

Stincic, T. L., Bosch, M. A., Hunker, A. C., Juarez, B., Connors, A. M., Zweifel, L. S., Rønnekleiv, O. K., & Kelly, M. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.28.122341 · Cited by 2

Biological Rhythms

Kriegsfeld, L. J., & Nelson, R. J. (2009) · doi:10.1002/9780470478509.neubb001005 · Cited by 2

Metabolism Connects Body, Brain, and Behavior

Horváth, T. L. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.03.015 · Cited by 1

Biological Contributors of Stress as a Common Factor across Overeating and Substance Use Disorders

Sinha, R. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780190671051.003.0024 · Cited by 1

Mechanisms of Homeostatically Regulated Behaviors

Elmquist, J. K., Zigman, J. M., & Saper, C. B. (2012) · Springer eBooks · doi:10.1007/978-1-4614-1997-6_62 · Cited by 1

A Desire for Parsimony

Cookson, L. J. (2013) · Behavioral Sciences · doi:10.3390/bs3040576 · Cited by 1

Control of Body Weight and the Modern Metabolic Diseases

Poian, A. T. D., & Castanho, M. A. R. B. (2015) · Springer eBooks · doi:10.1007/978-1-4939-3058-6_11 · Cited by 1

Glucagon-Like Peptide 1 and Human Obesity

Anandhakrishnan, A., & Korbonits, M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-48559-3.00003-8 · Cited by 1

Motivation

Bear, M. F., Connors, B. W., & Paradiso, M. A. (2018) · Springer eBooks · doi:10.1007/978-3-662-57263-4_16 · Cited by 1

Appetite Regulation and Thermogenesis

Maratos–Flier, E. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-5583-9.00027-7 · Cited by 1

Correlated changes in stress resistance and biochemical parameters in response to long-term protein restriction in Drosophila melanogaster

Krittika, S., & Yadav, P. (2024) · Royal Society Open Science · doi:10.1098/rsos.231741 · Cited by 1

Investigating the Reliability and Validity of the Power of Food Scale (PFS)

Ashrafi, E., Kachooei, M., & ghazaghi, M. (2015) · Knowledge & Research in Applied Psychology · Cited by 1

Beyond Homeostasis

Wilson, M. E., & Michopoulos, V. (2017) · CRC Press eBooks · doi:10.1201/9781315120171-4 · Cited by 1

The Anorectic Phenotype of the anx/anx Mouse Is Associated with Hypothalamic Dysfunction

Nilsson, I. A. K., Hökfelt, T. G. M., & Schalling, M. (2020) · Neuromethods · doi:10.1007/978-1-0716-0924-8_16 · Cited by 1

Control of Body Weight and the Modern Metabolic Diseases

Poian, A. T. D., & Castanho, M. A. R. B. (2021) · Springer eBooks · doi:10.1007/978-3-030-48740-9_11 · Cited by 1

Obesity: Peripheral Signals, Neural and Peptidergic

Karatsoreos, I. N., & Peters, J. H. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_155 · Cited by 1

Voluntary Food Intake of Pregnant and Non-pregnant Red Deer Hinds During the Gestating Period

Scott, I. (2011) · Lincoln University Research Archive (Lincoln University) · Cited by 1

THE PHYSIOLOGICAL ACTIONS OF ADIPONECTIN IN CENTRAL AUTONOMIC NUCLEI: IMPLICATIONS FOR THE INTEGRATIVE CONTROL OF ENERGY HOMEOSTASIS

Hoyda, T. D. (2010) · QSpace (Queen's University Library) · Cited by 1

The Mangalica Pig is a Novel Biomedical Model for Human Obesity and its Metabolic Complications

Roberts, M. (2015) · Cited by 1

The role of AgRP neurons as a central link between leptin receptors and fertility

Egan, O. K. (2016) · Otago University Research Archive (University of Otago) · Cited by 1

The Neuroendocrine Genome

Burbach, J. P. H. (2016) · Wiley eBooks · doi:10.1002/9781118760369.ch2 · Cited by 1

Ontogeny of Neuroendocrine Feeding Circuits

Croizier, S., & Bouret, S. G. (2016) · Wiley eBooks · doi:10.1002/9781118839317.ch3 · Cited by 1

Ghrelin - The Defender of Fat in the Face of Stress: Implications in Obesity Treatment

Patterson, Z. R. (2014) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2014-10055 · Cited by 1

Hypothalamic Control of Food Intake and Energy Homeostasis

Seoane, L. M., López, M., & Nogueiras, R. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.65178-4 · Cited by 1

Dinner for Two: Digging into how Ghrelin and Endocannabinoid Systems Interact in the Ventral Tegmental Area to Regulate Non-Homeostatic Feeding

Edwards, A. (2020) · doi:10.22215/etd/2020-14020 · Cited by 1

It Takes Two to Tango: Investigating the Relationship between Ghrelin and Endocannabinoids within the Ventral Tegmental Area with Regards to Feeding

Edwards, A. (2014) · doi:10.22215/etd/2014-10462 · Cited by 1

Neuroendocrine Regulation of Energy Metabolism

Dietrich, M. O., & Horváth, T. L. (2012) · Endocrinology and Metabolism · doi:10.3803/enm.2012.27.4.268 · Cited by 2

From neuroanatomy to behavior: central integration of peripheral signals regulating feeding behavior

Williams, K. W., & Elmquist, J. K. (2012) · Nature Neuroscience · doi:10.1038/nn.3217 · Cited by 435

Thoughts for Food: Brain Mechanisms and Peripheral Energy Balance

Abizaid, A. B., Gao, Q., & Horváth, T. L. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.025 · Cited by 122

Neuronal circuits that regulate feeding behavior and metabolism

Sohn, J., Elmquist, J. K., & Williams, K. W. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.05.003 · Cited by 282

and Reproductive Sciences

Abizaid, A. B., Gao, Q., & Horvath, T. L. (2013)