The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
Neurons for hunger and thirst transmit a negative-valence teaching signal
Open accessAbstract
Homeostasis is a biological principle for regulation of essential physiological parameters within a set range. Behavioural responses due to deviation from homeostasis are critical for survival, but motivational processes engaged by physiological need states are incompletely understood. We examined motivational characteristics of two separate neuron populations that regulate energy and fluid homeostasis by using cell-type-specific activity manipulations in mice. We found that starvation-sensitive AGRP neurons exhibit properties consistent with a negative-valence teaching signal. Mice avoided activation of AGRP neurons, indicating that AGRP neuron activity has negative valence. AGRP neuron inhibition conditioned preference for flavours and places. Correspondingly, deep-brain calcium imaging revealed that AGRP neuron activity rapidly reduced in response to food-related cues. Complementary experiments activating thirst-promoting neurons also conditioned avoidance. Therefore, these need-sensing neurons condition preference for environmental cues associated with nutrient or water ingestion, which is learned through reduction of negative-valence signals during restoration of homeostasis.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“A potentially similar function has been described for arcuate nucleus AgRP neurons and nitric oxide synthase 1 (NOS1) neurons in the subfornical organ (SFO). These neurons show heightened activity during hunger (AgRP) and thirst (NOS1), their activity elicits an aversive state (place avoidance), and they are essential for driving feeding and drinking behaviors, respectively21,227.”
From Neural mechanisms of social homeostasis (2019) · cites this paper as [227]
In the citing paper
“However, AgRP activity is rapidly suppressed on sensory detection of food227,228,230, which, surprisingly, suggests that ongoing AgRP activity is dispensable for food consumption.”
From Neural mechanisms of social homeostasis (2019) · cites this paper as [227]
In the citing paper
“AgRP neurons are activated in a state of energy deficit228, and their optical stimulation can voraciously promote food consumption, but also elicits real-time place avoidance (indicative of an aversive state) in the absence of food173,227,229.”
From Neural mechanisms of social homeostasis (2019) · cites this paper as [227]
In the citing paper
“However, a mouse may subsequently avoid a flavor that was paired with the AgRP neuronal stimulation that made it eat, leading some authors to suggest that stimulated hunger is necessarily an aversive drive that the mouse later associates with the flavor (Betley et al., 2015).”
From Evolving Concepts of Emotion and Motivation (2018) · cites this paper as Betley et al., 2015
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Ultrasensitive fluorescent proteins for imaging neuronal activity
Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474
Avants, B., Epstein, C. L., Grossman, M., & Gee, J. C. (2007) · Medical Image Analysis · doi:10.1016/j.media.2007.06.004 · Cited by 5,924
Skinner, B. F., & Hull, C. L. (1944) · The American Journal of Psychology · doi:10.2307/1416955 · Cited by 4,061
THE BIOLOGY OF HUMAN STARVATION
Keys, A., BROŽEK, J., & Henschel, A. (1951) · The Medical Journal of Australia · doi:10.5694/j.1326-5377.1951.tb56499.x · Cited by 2,135
The Biology of Human Starvation: Volume I
KEYS, A., BROŽEK, J., HENSCHEL, A., MICKELSEN, O., & TAYLOR, H. L. (1950) · doi:10.5749/j.ctv9b2tqv · Cited by 2,039
Stevens' Handbook of Experimental Psychology
Pashler, H. (2002) · Wiley eBooks · doi:10.1002/0471214426 · Cited by 1,713
Rapid, reversible activation of AgRP neurons drives feeding behavior in mice
Krashes, M. J., Koda, S., Ye, C., Rogan, S. C., Adams, A. C., Cusher, D. S., Maratos-Flier, E., Roth, B. L., & Lowell, B. B. (2011) · Journal of Clinical Investigation · doi:10.1172/jci46229 · Cited by 1,578
Cabanac, M. (1971) · Science · doi:10.1126/science.173.4002.1103 · Cited by 1,521
Two-process learning theory: Relationships between Pavlovian conditioning and instrumental learning.
Rescorla, R. A., & Solomon, R. L. (1967) · Psychological Review · doi:10.1037/h0024475 · Cited by 1,487
Conditioning and Associative Learning
Hill, W. F., & Mackintosh, N. J. (1984) · The American Journal of Psychology · doi:10.2307/1422540 · Cited by 1,304
Cited by
Sorted by citations
Items 101–200 of 702
Distinct speed dependence of entorhinal island and ocean cells, including respective grid cells
Sun, C., 北村, 貴., Yamamoto, J., Martin, J., Pignatelli, M., Kitch, L. J., Schnitzer, M. J., & Tonegawa, S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1511668112 · Cited by 123
Mohr, S. M., Bagriantsev, S. N., & Gracheva, E. O. (2020) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-012820-095945 · Cited by 133
Obesity causes selective and long-lasting desensitization of AgRP neurons to dietary fat
Beutler, L. R., Corpuz, T. V., Ahn, J. S., Kosar, S., Song, W., Chen, Y., & Knight, Z. A. (2020) · eLife · doi:10.7554/elife.55909 · Cited by 113
Habitual daily intake of a sweet and fatty snack modulates reward processing in humans
Thanarajah, S. E., DiFeliceantonio, A. G., Albus, K., Kuzmanovic, B., Rigoux, L., Iglesias, S., Hanßen, R., Schlamann, M., Cornely, O. A., Brüning, J. C., et al. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.02.015 · Cited by 131
Neural basis for fasting activation of the hypothalamic–pituitary–adrenal axis
Douglass, A. M., Resch, J. M., Madara, J. C., Kucukdereli, H., Yizhar, O., Grama, A., Yamagata, M., Yang, Z., & Lowell, B. B. (2023) · Nature · doi:10.1038/s41586-023-06358-0 · Cited by 123
Regulation of feeding by somatostatin neurons in the tuberal nucleus
Luo, S. X., Huang, J., Li, Q., Mohammad, H., Lee, C.-Y., Krishna, K., Kok, A. M. Y., Tan, Y. L., Lim, J., Li, H., et al. (2018) · Science · doi:10.1126/science.aar4983 · Cited by 115
Barbano, M. F., Wang, H., Morales, M., & Wise, R. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3799-15.2016 · Cited by 114
Multiple convergent hypothalamus–brainstem circuits drive defensive behavior
Lovett-Barron, M., Chen, R., Bradbury, S., Andalman, A. S., Wagle, M. D., Guo, S., & Deisseroth, K. A. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0655-1 · Cited by 116
Campos, A., Port, J. D., & Acosta, A. J. (2022) · Brain Sciences · doi:10.3390/brainsci12040431 · Cited by 126
Leptin-activated hypothalamic BNC2 neurons acutely suppress food intake
Tan, H. L., Yin, L., Tan, Y., Ivanov, J., Plucińska, K., Ilanges, A., Herb, B. R., Wang, P., Kosse, C., Cohen, P., et al. (2024) · Nature · doi:10.1038/s41586-024-08108-2 · Cited by 114
Multi-channel fiber photometry for population neuronal activity recording
Guo, Q., Zhou, J., Feng, Q., Lin, R., Gong, H., Luo, Q., Zeng, S., Luo, M., & Fu, L. (2015) · Biomedical Optics Express · doi:10.1364/boe.6.003919 · Cited by 107
Stamatakis, A. M., Schachter, M. J., Gulati, S., Zitelli, K. T., Malanowski, S., Tajik, A., Fritz, C., Trulson, M. O., & Otte, S. L. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00496 · Cited by 108
Resch, J. M., Fenselau, H., Madara, J. C., Wu, C., Campbell, J. N., Lyubetskaya, A., Dawes, B. A., Tsai, L. T.-Y., Li, M. M., Livneh, Y., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.014 · Cited by 104
Profound and redundant functions of arcuate neurons in obesity development
Zhu, C., Jiang, Z., Xu, Y., Cai, Z., Jiang, Q., Xu, Y., Xue, M., Arenkiel, B. R., Wu, Q., Shu, G., et al. (2020) · Nature Metabolism · doi:10.1038/s42255-020-0229-2 · Cited by 106
Hypothalamic tanycytes generate acute hyperphagia through activation of the arcuate neuronal network
Bolborea, M., Pollatzek, E., Benford, H., Sotelo-Hitschfeld, T., & Dale, N. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1919887117 · Cited by 100
TrpC5 Mediates Acute Leptin and Serotonin Effects via Pomc Neurons
Gao, Y., Yao, T. S., Deng, Z., Sohn, J., Sun, J. M., Huang, Y., Kong, X., Yu, K.-J., Wang, R.-T., Chen, H., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.072 · Cited by 101
New Neuroscience of Homeostasis and Drives for Food, Water, and Salt
Lowell, B. B. (2019) · New England Journal of Medicine · doi:10.1056/nejmra1812053 · Cited by 103
Hunger enhances food-odour attraction through a neuropeptide Y spotlight
Horio, N., & Liberles, S. D. (2021) · Nature · doi:10.1038/s41586-021-03299-4 · Cited by 101
Livneh, Y., & Andermann, M. L. (2021) · Neuron · doi:10.1016/j.neuron.2021.08.036 · Cited by 105
Singh, I., Wang, L., Xia, B., Liu, J., Tahiri, A., El Ouaamari, A., Wheeler, M. B., & Pang, Z. P. (2022) · Cell & Bioscience · doi:10.1186/s13578-022-00914-3 · Cited by 98
Hunger and Satiety Gauge Reward Sensitivity
Cassidy, R. M., & Tong, Q. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00104 · Cited by 93
Integrating Hunger with Rival Motivations
Hickey, A. K. S., & Krashes, M. J. (2020) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2020.04.006 · Cited by 96
Bidirectional Anticipation of Future Osmotic Challenges by Vasopressin Neurons
Mandelblat-Cerf, Y., Kim, A., Burgess, C. R., Subramanian, S., Tannous, B. A., Lowell, B. B., & Andermann, M. L. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.021 · Cited by 98
Xu, Y., Lu, Y., Cassidy, R. M., Mangieri, L. R., Zhu, C., Xugen, H., Jiang, Z., Justice, N. J., Xu, Y., Arenkiel, B. R., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11399-z · Cited by 98
Gaspar, J. M., & Velloso, L. A. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00813 · Cited by 97
Hypothalamic Neurons that Regulate Feeding Can Influence Sleep/Wake States Based on Homeostatic Need
Goldstein, N., Levine, B. J., Loy, K. A., Duke, W. L., Meyerson, O. S., Jamnik, A. A., & Carter, M. E. (2018) · Current Biology · doi:10.1016/j.cub.2018.09.055 · Cited by 99
Dopamine tunes prefrontal outputs to orchestrate aversive processing
Weele, C. M. V., Siciliano, C. A., & Tye, K. M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.11.044 · Cited by 98
Food cue regulation of AGRP hunger neurons guides learning
Berrios, J., Li, C., Madara, J. C., Garfield, A. S., Steger, J. S., Krashes, M. J., & Lowell, B. B. (2021) · Nature · doi:10.1038/s41586-021-03729-3 · Cited by 88
Interactions between central nervous system and peripheral metabolic organs
Zeng, W., Yang, F., Shen, W. L., Zhan, C., Zheng, P., & Hu, J. (2022) · Science China Life Sciences · doi:10.1007/s11427-021-2103-5 · Cited by 103
The cellular basis of distinct thirst modalities
Pool, A., Wang, T., Stafford, D. A., Chance, R. K., Lee, S., Ngai, J., & Oka, Y. (2020) · Nature · doi:10.1038/s41586-020-2821-8 · Cited by 92
Wallace, C. W., & Fordahl, S. C. (2021) · Nutrition Research Reviews · doi:10.1017/s0954422421000196 · Cited by 98
Hindbrain Double-Negative Feedback Mediates Palatability-Guided Food and Water Consumption
Gong, R., Xu, S., Hermundstad, A. M., Yu, Y., & Sternson, S. M. (2020) · Cell · doi:10.1016/j.cell.2020.07.031 · Cited by 81
Self-citationTorruella-Suárez, M. L., Vandenberg, J. R., Cogan, E. S., Tipton, G. J., Teklezghi, A. T., Dange, K., Patel, G., McHenry, J. A., Hardaway, J. A., Kantak, P. A., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1466-19.2019 · Cited by 87
Neurobiology of eating behavior, nutrition, and health
Stover, P. J., Field, M. S., Andermann, M. L., Bailey, R. L., Batterham, R. L., Cauffman, E. E., Frühbeck, G., Iversen, P. O., Starke-Reed, P. E., Sternson, S. M., et al. (2023) · Journal of Internal Medicine · doi:10.1111/joim.13699 · Cited by 91
Self-citationMetabolic and Kidney Diseases in the Setting of Climate Change, Water Shortage, and Survival Factors
Johnson, R. J., Stenvinkel, P., Jensen, T., Lanaspa, M. A., Roncal, C., Song, Z., Bankir, L., & Sánchez‐Lozada, L. G. (2016) · Journal of the American Society of Nephrology · doi:10.1681/asn.2015121314 · Cited by 90
Making sense of the sensory regulation of hunger neurons
Chen, Y., & Knight, Z. A. (2016) · BioEssays · doi:10.1002/bies.201500167 · Cited by 88
Al–Massadi, O., Nogueiras, R., Diéguez, C., & Girault, J. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.01.001 · Cited by 81
Temporally and Spatially Distinct Thirst Satiation Signals
Augustine, V., Ebisu, H., Zhao, Y., Lee, S., Ho, B., Mizuno, G. O., Tian, L., & Oka, Y. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.039 · Cited by 79
A neural circuit for male sexual behavior and reward
Bayless, D. W., Davis, C.-H. O., Yang, R., Wei, Y., Carvalho, V. M. D. A., Knoedler, J. R., Yang, T., Livingston, O., Lomvardas, A., Martins, G. J., et al. (2023) · Cell · doi:10.1016/j.cell.2023.07.021 · Cited by 94
Mátyás, F., Komlósi, G., Babiczky, Á., Kocsis, K., Barthó, P., Barsy, B., Dávid, C., Kanti, V., Porrero, C., Magyar, A., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0251-9 · Cited by 83
Reward Contributions to Serotonergic Functions
Liu, Z., Lin, R., & Luo, M. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-093019-112252 · Cited by 79
Stress and obesity: The ghrelin connection
Abizaid, A. B. (2019) · Journal of Neuroendocrinology · doi:10.1111/jne.12693 · Cited by 83
McKinley, M. J., Denton, D. A., Ryan, P. J., Yao, S. T., Stefanidis, A., & Oldfield, B. J. (2019) · Journal of Neuroendocrinology · doi:10.1111/jne.12689 · Cited by 79
Okamoto, S., Sato, T., Tateyama, M., Kageyama, H., Maejima, Y., Nakata, M., Hirako, S., Matsuo, T., Kyaw, S., Shiuchi, T., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.11.102 · Cited by 75
Expressions of emotions across species
Zych, A. D., & Gogolla, N. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.01.003 · Cited by 85
MRAP2 regulates ghrelin receptor signaling and hunger sensing
Srisai, D., Yin, T. C., Lee, A. A., Rouault, A. A. J., Pearson, N. A., Grobe, J. L., & Sebag, J. A. (2017) · Nature Communications · doi:10.1038/s41467-017-00747-6 · Cited by 79
A bidirectional network for appetite control in larval zebrafish
Wee, C. L., Song, E. Y., Johnson, R. E., Ailani, D., Randlett, O., Kim, J.-Y., Nikitchenko, M., Bahl, A., Yang, C.-T., Ahrens, M. B., et al. (2019) · eLife · doi:10.7554/elife.43775 · Cited by 73
Heterogeneous pericoerulear neurons tune arousal and exploratory behaviours
Luskin, A. T., Li, L., Fu, X., Martin, M. M., Barcomb, K., Girven, K. S., Blackburn, T., Wells, B. A., Thai, S., Li, E. M., et al. (2025) · Nature · doi:10.1038/s41586-025-08952-w · Cited by 68
MCH Neurons Regulate Permeability of the Median Eminence Barrier
Jiang, H., Gallet, S., Klemm, P., Scholl, P., Folz‐Donahue, K., Altmüller, J., Alber, J., Heilinger, C., Kukat, C., Loyens, A., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.04.020 · Cited by 78
Learning of food preferences: mechanisms and implications for obesity & metabolic diseases
Berthoud, H., Morrison, C. D., Ackroff, K., & Sclafani, A. J. (2021) · International Journal of Obesity · doi:10.1038/s41366-021-00894-3 · Cited by 81
Hedonic eating is controlled by dopamine neurons that oppose GLP-1R satiety
Zhu, Z., Gong, R., Rodriguez, V., Quach, K. T., Chen, X., & Sternson, S. M. (2025) · Science · doi:10.1126/science.adt0773 · Cited by 85
Self-citationThe neuroscience of sugars in taste, gut-reward, feeding circuits, and obesity
Gutiérrez, R., Fonseca, E., & Simon, S. A. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03458-2 · Cited by 72
Role of Somatostatin in the Regulation of Central and Peripheral Factors of Satiety and Obesity
Kumar, U., & Singh, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072568 · Cited by 73
Preclinical models for obesity research
Barrett, P., Mercer, J. G., & Morgan, P. J. (2016) · Disease Models & Mechanisms · doi:10.1242/dmm.026443 · Cited by 78
AGRP Neurons Project to the Medial Preoptic Area and Modulate Maternal Nest-Building
Li, X., Han, Y., Zhang, W., Wang, S.-R., Wei, Y., Li, S., Lin, J.-K., Yan, J.-J., Chen, A.-X., Zhang, X., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0958-18.2018 · Cited by 74
Need-based prioritization of behavior
Burnett, C. J., Funderburk, S. C., Navarrete, J. S., Sabol, A., Liang-Guallpa, J., Desrochers, T. M., & Krashes, M. J. (2019) · eLife · doi:10.7554/elife.44527 · Cited by 71
Functional Ontogeny of Hypothalamic Agrp Neurons in Neonatal Mouse Behaviors
Zimmer, M. R., Fonseca, A. H. O., İyilikci, O., Pra, R. D., & Dietrich, M. O. (2019) · Cell · doi:10.1016/j.cell.2019.04.026 · Cited by 71
Serotonergic neurons translate taste detection into internal nutrient regulation
Yao, Z., & Scott, K. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.028 · Cited by 74
Targeting the central melanocortin system for the treatment of metabolic disorders
Sweeney, P., Gimenez, L. E., Hernández, C. C., & Cone, R. D. (2023) · Nature Reviews Endocrinology · doi:10.1038/s41574-023-00855-y · Cited by 71
Chemosensory modulation of neural circuits for sodium appetite
Lee, S., Augustine, V., Zhao, Y. Z., Ebisu, H., Ho, B., Kong, D., & Oka, Y. (2019) · Nature · doi:10.1038/s41586-019-1053-2 · Cited by 68
Inhibition of impulsive action by projection-defined prefrontal pyramidal neurons
Li, B., Nguyen, T. P., Ma, C., & Dan, Y. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2000523117 · Cited by 70
Hypothalamic control of interoceptive hunger
Siemian, J. N., Arenivar, M. A., Sarsfield, S., & Aponte, Y. (2021) · Current Biology · doi:10.1016/j.cub.2021.06.048 · Cited by 64
Hypothalamic mTORC2 is essential for metabolic health and longevity
Chellappa, K., Brinkman, J. A., Mukherjee, S., Morrison, M., Alotaibi, M. I., Carbajal, K. A., Alhadeff, A. L., Perron, I. J., Yao, R., Purdy, C. S., et al. (2019) · Aging Cell · doi:10.1111/acel.13014 · Cited by 62
Self-citationA Hypothalamic Phosphatase Switch Coordinates Energy Expenditure with Feeding
Dodd, G. T., Andrews, Z. B., Simonds, S. E., Michael, N. J., DeVeer, M., Brüning, J. C., Spanswick, D., Cowley, M. A., & Tiganis, T. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.07.013 · Cited by 66
The neural basis of sugar preference
Liu, W. W., & Bohórquez, D. V. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00613-5 · Cited by 65
Averbeck, B. B., & Murray, E. A. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.06.006 · Cited by 64
A neuronal ensemble encoding adaptive choice during sensory conflict in Drosophila
Sareen, P., McCurdy, L. Y., & Nitabach, M. N. (2021) · Nature Communications · doi:10.1038/s41467-021-24423-y · Cited by 66
Toggling between food-seeking and self-preservation behaviors via hypothalamic response networks
Salgado, I. D. A., Li, C., Burnett, C. J., Rodriguez-Gonzalez, S., Becker, J. J., Horvath, A., Earnest, T., Kravitz, A. V., & Krashes, M. J. (2023) · Neuron · doi:10.1016/j.neuron.2023.06.006 · Cited by 61
Stuber, G. D. (2023) · Science · doi:10.1126/science.adh8287 · Cited by 69
Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding
Luskin, A. T., Bhatti, D. L., Mulvey, B., Pedersen, C. E., Girven, K. S., Oden-Brunson, H., Kimbell, K., Blackburn, T., Sawyer, A., Gereau, R. W., et al. (2021) · Science Advances · doi:10.1126/sciadv.abd3666 · Cited by 63
Neural Circuit Mechanisms Underlying Emotional Regulation of Homeostatic Feeding
Sweeney, P., & Yang, Y. (2017) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2017.02.006 · Cited by 67
Central Ghrelin Resistance Permits the Overconsolidation of Fear Memory
Harmatz, E. S., Stone, L. A., Lim, S. H., Lee, G. L., McGrath, A. G., Gisabella, B., Peng, X., Kosoy, E., Yao, J., Liu, E. E., et al. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.11.009 · Cited by 61
Huang, R., Song, T., Su, H., Lai, Z., Qin, W., Tian, Y., Dong, X., & Wang, L. (2020) · eLife · doi:10.7554/elife.53103 · Cited by 62
Regulation of feeding related behaviours by Arcuate neuropeptide Y neurons
Zhang, L., Hernández-Sánchez, D., & Herzog, H. (2019) · Endocrinology · doi:10.1210/en.2019-00056 · Cited by 65
Recurrent Circuitry Sustains Drosophila Courtship Drive While Priming Itself for Satiety
Zhang, S. X., Rogulja, D., & Crickmore, M. A. (2019) · Current Biology · doi:10.1016/j.cub.2019.08.015 · Cited by 61
Drugs of abuse hijack a mesolimbic pathway that processes homeostatic need
Tan, B., Browne, C. J., Nöbauer, T., Vaziri, A., Friedman, J. M., & Nestler, E. J. (2024) · Science · doi:10.1126/science.adk6742 · Cited by 61
DREADD-induced activation of subfornical organ neurons stimulates thirst and salt appetite
Nation, H. L., Nicoleau, M., Kinsman, B. J., Browning, K. N., & Stocker, S. D. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00149.2016 · Cited by 60
Somatostatin Neurons in the Basal Forebrain Promote High-Calorie Food Intake
Zhu, C., Yao, Y., Xiong, Y., Cheng, M., Chen, J. W., Zhao, R., Liao, F., Shi, R., & Song, S. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.06.007 · Cited by 58
Brain to bone: What is the contribution of the brain to skeletal homeostasis?
Idelevich, A., & Baron, R. (2018) · Bone · doi:10.1016/j.bone.2018.05.018 · Cited by 62
Cold-induced hyperphagia requires AgRP neuron activation in mice
Deem, J. D., Faber, C. L., Pedersen, C. E., Phan, B. A., Larsen, S. A., Ogimoto, K., Nelson, J. T., Damian, V. M., Tran, M. A., Palmiter, R. D., et al. (2020) · eLife · doi:10.7554/elife.58764 · Cited by 58
A synaptic amplifier of hunger for regaining body weight in the hypothalamus
Grzelka, K., Wilhelms, H. E., Dodt, S., Dreisow, M.-L., Madara, J. C., Walker, S. J., Wu, C., Wang, D., Lowell, B. B., & Fenselau, H. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.03.002 · Cited by 64
Fasano, A. (2025) · New England Journal of Medicine · doi:10.1056/nejmra2402679 · Cited by 69
Diet-induced obesity causes ghrelin resistance in reward processing tasks
Lockie, S. H., Dinan, T., Lawrence, A. J., Spencer, S. J., & Andrews, Z. B. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.08.004 · Cited by 58
New insight into GABAergic neurons in the hypothalamic feeding regulation
Suyama, S., & Yada, T. (2018) · The Journal of Physiological Sciences · doi:10.1007/s12576-018-0622-8 · Cited by 60
Motivation, Perception, and Chance Converge to Make a Binary Decision
Zhang, S. X., Miner, L. E., Boutros, C. L., Rogulja, D., & Crickmore, M. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.06.014 · Cited by 62
Reichenbach, A., Clarke, R., Stark, R., Lockie, S. H., Méquinion, M., Dempsey, H., Rawlinson, S., Reed, F. M., Sepehrizadeh, T., DeVeer, M., et al. (2022) · eLife · doi:10.7554/elife.72668 · Cited by 57
Nutrient homeostasis — translating internal states to behavior
Münch, D., Ezra-Nevo, G., Francisco, A. P., Tastekin, I., & Ribeiro, C. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.10.004 · Cited by 52
The Role of the Melanocortin System in Metabolic Disease: New Developments and Advances
Hill, J. W., & Faulkner, L. D. (2016) · Neuroendocrinology · doi:10.1159/000450649 · Cited by 57
Cassidy, R. M., Lu, Y., Jere, M., Tian, J., Xu, Y., Mangieri, L. R., Felix-Okoroji, B., Selever, J., Xu, Y., Arenkiel, B. R., et al. (2019) · Science Advances · doi:10.1126/sciadv.aav1640 · Cited by 58
Preemptive Stimulation of AgRP Neurons in Fed Mice Enables Conditioned Food Seeking under Threat
Jikomes, N., Ramesh, R. N., Mandelblat-Cerf, Y., & Andermann, M. L. (2016) · Current Biology · doi:10.1016/j.cub.2016.07.019 · Cited by 58
Parallels and Overlap: The Integration of Homeostatic Signals by Mesolimbic Dopamine Neurons
Hsu, T. M., McCutcheon, J. E., & Roitman, M. F. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00410 · Cited by 59
Thirst and Drinking Paradigms: Evolution from Single Factor Effects to Brainwide Dynamic Networks
Armstrong, L. E., & Kavouras, S. A. (2019) · Nutrients · doi:10.3390/nu11122864 · Cited by 63
Stochastic neuropeptide signals compete to calibrate the rate of satiation
Zhang, S. X., Kim, A., Madara, J. C., Zhu, P. K., Christenson, L. F., Lutas, A., Kalugin, P. N., Sunkavalli, P. S., Jin, Y., Pal, A., et al. (2024) · Nature · doi:10.1038/s41586-024-08164-8 · Cited by 65
Rau, A. R., & Hentges, S. T. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0647-17.2017 · Cited by 60
Antonini, A., Sattin, A., Moroni, M., Bovetti, S., Moretti, C., Succol, F., Forli, A., Vecchia, D., Rajamanickam, V. P., Bertoncini, A., et al. (2020) · eLife · doi:10.7554/elife.58882 · Cited by 56
AgRP neurons encode circadian feeding time
Sayar, N., Aklan, İ., Yavuz, Y., Laule, C. F., Kim, H., Rysted, J., Alp, M. İ., Davis, D., Yılmaz, B., & Atasoy, D. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01482-6 · Cited by 56
Brain control of energy homeostasis: implications for anti-obesity pharmacotherapy
Johansen, V. B. I., Petersen, J., Lund, J., Mathiesen, C. V., Fenselau, H., & Clemmensen, C. (2025) · Cell · doi:10.1016/j.cell.2025.06.010 · Cited by 53
An Emerging Technology Framework for the Neurobiology of Appetite
Sternson, S. M., Atasoy, D., Betley, J. N., Henry, F. E., & Xu, S. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.12.002 · Cited by 56
Self-citationBerthoud, H., Morrison, C. D., & Münzberg, H. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.112959 · Cited by 61
Brain circuits for promoting homeostatic and non-homeostatic appetites
Ahn, B. H., Kim, M., & Kim, S. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00758-4 · Cited by 53
Metadata
- Authors
- Betley, J. N., Xu, S., Cao, Z. F. H., Gong, R., Magnus, C. J., Yu, Y., & Sternson, S. M.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Sternson, Scott M.
- ORCID
- Venue
- Nature
- Published
- 2015-04-27
- Volume
- 521
- Issue
- 7551
- Pages
- 180-185
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4567040
- OpenAlex
- W2101995469
- Cited by
- 704
- References
- 49
- Citations by year
- 2026: 32 · 2025: 73 · 2024: 70 · 2023: 68 · 2022: 50 · 2021: 72 · 2020: 65 · 2019: 73 · 2018: 64 · 2017: 62 · 2016: 54 · 2015: 21
- FWCI
- 37.15
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- hunger, thirst, homeostasis, AgRP neurons, subfornical organ, negative valence, teaching signal, motivation in learning, avoidance conditioning, energy homeostasis, fluid homeostasis
- MeSH terms
- Animals, Cues, Dehydration, Drinking, Eating, Food, Food Preferences, Homeostasis, Hunger, Hypothalamus, Male, Neurons, Starvation, Thirst, Models, Animal, Mice, Agouti-Related Protein
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review