Overlapping Brain Circuits for Homeostatic and Hedonic Feeding
Open accessAbstract
Central regulation of food intake is a key mechanism contributing to energy homeostasis. Many neural circuits that are thought to orchestrate feeding behavior overlap with the brain's reward circuitry both anatomically and functionally. Manipulation of numerous neural pathways can simultaneously influence food intake and reward. Two key systems underlying these processes-those controlling homeostatic and hedonic feeding-are often treated as independent. Homeostatic feeding is necessary for basic metabolic processes and survival, while hedonic feeding is driven by sensory perception or pleasure. Despite this distinction, their functional and anatomical overlap implies considerable interaction that is often overlooked. Here, we argue that the neurocircuits controlling homeostatic feeding and hedonic feeding are not completely dissociable given the current data and urge researchers to assess behaviors extending beyond food intake in investigations of the neural control of feeding.
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
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?
Feeding behavior is directed by motivational drives of opposing valence: the negative sensation of hunger and the positive hedonic value of palatable food.
“Feeding behavior, therefore, is directed by motivational drives of opposing valence: the negative sensation of hunger and the positive hedonic value of palatable food.”
From Neural mechanisms of social homeostasis (2019) · cites this paper as [217]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
An Integrative Theory of Prefrontal Cortex Function
Miller, E. K., & Cohen, J. D. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.167 · Cited by 12,803 · see citing works
Dopamine, learning and motivation.
Wise, R. A. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1406 · Cited by 3,379 · cited 1× · see citing works
“For more than half a century, scientists have struggled to understand the intermingled neural basis of reward and feeding (Berridge, 1996; Hoebel and Teitelbaum, 1962; Margules and Olds, 1962; Wise, 2004).”
BackgroundTargeted disruption of the melanocortin-4 receptor results in obesity in mice
Huszar, D., Lynch, C. A., Fairchild-Huntress, V., Dunmore, J. H., Fang, Q., Berkemeier, L. R., Gu, W., Kesterson, R. A., Boston, B. A., Cone, R. D., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)81865-6 · Cited by 3,030 · see citing works
Getting formal with dopamine and reward
Schultz, W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00967-4 · Cited by 2,574 · see citing works
Central nervous system control of food intake and body weight
Morton, G. J., Cummings, D. E., Baskin, D. G., Barsh, G. S., & Schwartz, M. W. (2006) · Nature · doi:10.1038/nature05026 · Cited by 2,503 · see citing works
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 · see citing works
Food reward: brain substrates of wanting and liking
Berridge, K. C. (1996) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00033-b · Cited by 1,901 · see citing works
Wang, G.-J., Volkow, N. D., Logan, J., Pappas, N. R., Wong, C. T., Zhu, W., Netusll, N., & Fowler, J. S. (2001) · The Lancet · doi:10.1016/s0140-6736(00)03643-6 · Cited by 1,864 · see citing works
The Amygdaloid Complex: Anatomy and Physiology
SAH, P., FABER, E. S. L., LOPEZ DE ARMENTIA, M., & POWER, J. (2003) · Physiological Reviews · doi:10.1152/physrev.00002.2003 · Cited by 1,745 · see citing works
Anatomy and regulation of the central melanocortin system
Cone, R. D. (2005) · Nature Neuroscience · doi:10.1038/nn1455 · Cited by 1,583 · see citing works
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 · see citing works
Dopamine D2 receptors in addiction-like reward dysfunction and compulsive eating in obese rats
Johnson, P. M., & Kenny, P. J. (2010) · Nature Neuroscience · doi:10.1038/nn.2519 · Cited by 1,495 · see citing works
The mysterious motivational functions of mesolimbic dopamine
Salamone, J. D., & Correa, M. (2012) · Neuron · doi:10.1016/j.neuron.2012.10.021 · Cited by 1,418 · see citing works
Reward, dopamine and the control of food intake: implications for obesity
Volkow, N. D., Wang, G.-J., & Baler, R. D. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.11.001 · Cited by 1,400 · see citing works
A role for lateral hypothalamic orexin neurons in reward seeking
Harris, G. C., Wimmer, M., & Aston-Jones, G. (2005) · Nature · doi:10.1038/nature04071 · Cited by 1,311 · see citing works
Input-specific control of reward and aversion in the ventral tegmental area
Lammel, S., Lim, B. K., Ran, C., Huang, K. W., Betley, M. J., Tye, K. M., Deisseroth, K., & Malenka, R. C. (2012) · Nature · doi:10.1038/nature11527 · Cited by 1,300 · see citing works
Ungerstedt, U. (1971) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.1971.tb11001.x · Cited by 1,294 · see citing works
Amygdala circuitry mediating reversible and bidirectional control of anxiety
Tye, K. M., Prakash, R., Kim, S.-Y., Fenno, L. E., Grosenick, L., Zarabi, H., Thompson, K. R., Gradinaru, V., Ramakrishnan, C., & Deisseroth, K. (2011) · Nature · doi:10.1038/nature09820 · Cited by 1,289 · see citing works
Eating disorder and epilepsy in mice lacking 5-HT2C serotonin receptors
Tecott, L. H., Sun, L. M., Akana, S. F., Strack, A. M., Lowenstein, D. H., Dallman, M. F., & Julius, D. J. (1995) · Nature · doi:10.1038/374542a0 · Cited by 1,275 · see citing works
Phasic Firing in Dopaminergic Neurons Is Sufficient for Behavioral Conditioning
Tsai, H.-C., Zhang, F., Adamantidis, A., Stuber, G. D., Bonci, A., de Lecea, L., & Deisseroth, K. (2009) · Science · doi:10.1126/science.1168878 · Cited by 1,266 · see citing works
Self-citationBaxter, M. G., & Murray, E. A. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn875 · Cited by 1,200 · see citing works
Hypothalamic control of food intake in rats and cats.
Anand, B. K., & Brobeck, J. R. (1951) · PubMed · Cited by 1,197 · see citing works
Coexpression of Agrp and NPY in fasting-activated hypothalamic neurons
Hahn, T. M., Breininger, J. F., Baskin, D. G., & Schwartz, M. W. (1998) · Nature Neuroscience · doi:10.1038/1082 · Cited by 1,164 · see citing works
Elmquist, J. K., Elias, C. F., & Saper, C. B. (1999) · Neuron · doi:10.1016/s0896-6273(00)81084-3 · Cited by 1,160 · see citing works
AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training
Aponte, Y., Atasoy, D., & Sternson, S. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2739 · Cited by 1,157 · see citing works
NPY/AgRP Neurons Are Essential for Feeding in Adult Mice but Can Be Ablated in Neonates
Luquet, S. H., Perez, F. A., Hnasko, T. S., & Palmiter, R. D. (2005) · Science · doi:10.1126/science.1115524 · Cited by 1,127 · see citing works
Saper, C. B., Chou, T. C., & Elmquist, J. K. (2002) · Neuron · doi:10.1016/s0896-6273(02)00969-8 · Cited by 1,120 · see citing works
Expression of ghrelin receptor mRNA in the rat and the mouse brain
Zigman, J. M., Jones, J. E., Lee, C. E., Saper, C. B., & Elmquist, J. K. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20823 · Cited by 1,074 · see citing works
Circuit architecture of VTA dopamine neurons revealed by systematic input-output mapping
Beier, K. T., Steinberg, E. E., DeLoach, K. E., Xie, S., Miyamichi, K., Schwarz, L., Gao, X. J., Kremer, E. J., Malenka, R. C., & Luo, L. (2015) · Cell · doi:10.1016/j.cell.2015.07.015 · Cited by 1,068 · see citing works
Subnuclear organization of the efferent connections of the parabrachial nucleus in the rat
Fulwiler, C., & Saper, C. B. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90012-2 · Cited by 1,057 · see citing works
Abizaid, A., Liu, Z.-W., Andrews, Z. B., Shanabrough, M., Borok, E., Elsworth, J. D., Roth, R. H., Sleeman, M. W., Picciotto, M. R., Tschöp, M. H., et al. (2006) · Journal of Clinical Investigation · doi:10.1172/jci29867 · Cited by 984 · see citing works
Deconstruction of a neural circuit for hunger
Atasoy, D., Betley, J. N., Su, H. H., & Sternson, S. M. (2012) · Nature · doi:10.1038/nature11270 · Cited by 969 · see citing works
Kelley, A. E. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2003.11.015 · Cited by 942 · see citing works
Leptin Differentially Regulates NPY and POMC Neurons Projecting to the Lateral Hypothalamic Area
Elias, C. F., Aschkenasi, C., Lee, C., Kelly, J., Ahima, R. S., Bjorbæk, C., Flier, J. S., Saper, C. B., & Elmquist, J. K. (1999) · Neuron · doi:10.1016/s0896-6273(01)80035-0 · Cited by 924 · see citing works
Leptin Receptor Signaling in Midbrain Dopamine Neurons Regulates Feeding
Hommel, J. D., Trinko, R., Sears, R. M., Georgescu, D., Liu, Z.-W., Gao, X.-B., Thurmon, J. J., Marinelli, M., & DiLeone, R. J. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.023 · Cited by 902 · see citing works
Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity
Vaisse, C., Clement, K., Durand, E., Hercberg, S., Guy-Grand, B., & Froguel, P. (2000) · Journal of Clinical Investigation · doi:10.1172/jci9238 · Cited by 897 · see citing works
Teitelbaum, P., & Epstein, A. N. (1962) · Psychological Review · doi:10.1037/h0039285 · Cited by 884 · see citing works
Excitatory transmission from the amygdala to nucleus accumbens facilitates reward seeking
Stuber, G. D., Sparta, D. R., Stamatakis, A. M., van Leeuwen, W. A., Hardjoprajitno, J. E., Cho, S., Tye, K. M., Kempadoo, K. A., Zhang, F., Deisseroth, K., et al. (2011) · Nature · doi:10.1038/nature10194 · Cited by 878 · see citing works
Self-citationRole of the bed nucleus of the stria terminalis versus the amygdala in fear, stress, and anxiety
Walker, D. L., Toufexis, D. J., & Davis, M. (2003) · European Journal of Pharmacology · doi:10.1016/s0014-2999(03)01282-2 · Cited by 838 · see citing works
Agouti-related peptide–expressing neurons are mandatory for feeding
Gropp, E., Shanabrough, M., Borók, E., Xu, A. W., Janoschek, R., Buch, T., Plum, L., Balthasar, N., Hampel, B., Waisman, A., et al. (2005) · Nature Neuroscience · doi:10.1038/nn1548 · Cited by 800 · see citing works
Proopiomelanocortin Neurons Are Direct Targets for Leptin in the Hypothalamus
Cheung, C. C., Clifton, D. K., & Steiner, R. A. (1997) · Endocrinology · doi:10.1210/endo.138.10.5570 · Cited by 769 · cited 1× · see citing works
“They tend to co-express b-endorphin and cocaine-amphetamine-regulated transcript and are responsive to circulating hormones including leptin and insulin (Cheung et al., 1997; Cone et al., 2001; Cowley et al., 2001).”
BackgroundDopamine-deficient mice are severely hypoactive, adipsic, and aphagic
Zhou, Q.-Y., & Palmiter, R. D. (1995) · Cell · doi:10.1016/0092-8674(95)90145-0 · Cited by 731 · see citing works
Dopamine operates as a subsecond modulator of food seeking
Roitman, M. F., Stuber, G. D., Phillips, P. E. M., Wightman, R. M., & Carelli, R. M. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3823-03.2004 · Cited by 718 · see citing works
Self-citationDistinct extended amygdala circuits for divergent motivational states
Jennings, J. H., Sparta, D. R., Stamatakis, A. M., Ung, R. L., Pleil, K. E., Kash, T. L., & Stuber, G. D. (2013) · Nature · doi:10.1038/nature12041 · Cited by 704 · cited 6× · see citing works
“Intracranial selfstimulation sites, which depend on dopamine release, have often been found to promote feeding and depend on the current satiety state of the subject (Abrahamsen et al., 1995; Adamantidis et al., 2011; Carr and Wolinsky, 1993; Jennings et al., 2013a; Stuber et al., 2011).”
BackgroundInfluentialSelf-citationNeurons for hunger and thirst transmit a negative-valence teaching signal
Betley, J. N., Xu, S., Cao, Z. F. H., Gong, R., Magnus, C. J., Yu, Y., & Sternson, S. M. (2015) · Nature · doi:10.1038/nature14416 · Cited by 704 · see citing works
Synaptic release of GABA by AgRP neurons is required for normal regulation of energy balance
Tong, Q., Ye, C.-P., Jones, J. E., Elmquist, J. K., & Lowell, B. B. (2008) · Nature Neuroscience · doi:10.1038/nn.2167 · Cited by 689 · see citing works
Witten, I. B., Steinberg, E. E., Lee, S. Y., Davidson, T. J., Zalocusky, K. A., Brodsky, M., Yizhar, O., Cho, S. L., Gong, S., Ramakrishnan, C., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.028 · Cited by 680 · see citing works
Self-citationGhrelin Modulates Brain Activity in Areas that Control Appetitive Behavior
Malik, S., McGlone, F., Bedrossian, D., & Dagher, A. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2008.03.007 · Cited by 677 · see citing works
Localization of a "Feeding Center" in the Hypothalamus of the Rat
Anand, B. K., & Brobeck, J. R. (1951) · Experimental Biology and Medicine · doi:10.3181/00379727-77-18766 · Cited by 670 · see citing works
Neuroreptide Y: Stimulation of feeding and drinking by injection into the paraventricular nucleus
Stanley, B. G., & LEIBOWITZ, S. F. (1984) · Life Sciences · doi:10.1016/0024-3205(84)90032-8 · Cited by 665 · see citing works
Sensory Detection of Food Rapidly Modulates Arcuate Feeding Circuits
Chen, Y., Lin, Y.-C., Kuo, T.-W., & Knight, Z. A. (2015) · Cell · doi:10.1016/j.cell.2015.01.033 · Cited by 660 · see citing works
Parkinsonian-like locomotor impairment in mice lacking dopamine D2 receptors
Baik, J., Picetti, R., Saiardi, A., Thiriet, G., Dierich, A., Depaulis, A., LeMeur, M., & Borrelli, E. (1995) · Nature · doi:10.1038/377424a0 · Cited by 651 · see citing works
Leptin Regulation of the Mesoaccumbens Dopamine Pathway
Fulton, S., Pissios, P., Manchon, R. P., Stiles, L., Frank, L., Pothos, E. N., Maratos-Flier, E., & Flier, J. S. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.006 · Cited by 644 · see citing works
De Araujo, I. E. T., Rolls, E. T., Kringelbach, M. L., McGlone, F., & Phillips, N. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02915.x · Cited by 642 · see citing works
The role of SOCS-3 in leptin signaling and leptin resistance
Bjørbæk, C., El-Haschimi, K., Frantz, J. D., & Flier, J. S. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.42.30059 · Cited by 639 · see citing works
GABA Neurons of the VTA Drive Conditioned Place Aversion
Tan, K. R., Yvon, C., Turiault, M., Mirzabekov, J. J., Doehner, J., Labouèbe, G., Deisseroth, K. A., Tye, K. M., & Lüscher, C. (2012) · Neuron · doi:10.1016/j.neuron.2012.02.015 · Cited by 635 · see citing works
Small, D. M., Jones-Gotman, M., & Dagher, A. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00253-2 · Cited by 632 · see citing works
Hernandez, L., & Hoebel, B. G. (1988) · Life Sciences · doi:10.1016/0024-3205(88)90036-7 · Cited by 627 · see citing works
Integration of NPY, AGRP, and Melanocortin Signals in the Hypothalamic Paraventricular Nucleus
Cowley, M. A., Pronchuk, N., Fan, W., Dinulescu, D. M., Colmers, W. F., & Cone, R. D. (1999) · Neuron · doi:10.1016/s0896-6273(00)80829-6 · Cited by 616 · see citing works
Activation of VTA GABA Neurons Disrupts Reward Consumption
van Zessen, R., Phillips, J. L., Budygin, E. A., & Stuber, G. D. (2012) · Neuron · doi:10.1016/j.neuron.2012.02.016 · Cited by 609 · see citing works
Self-citationAn excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger
Krashes, M. J., Shah, B. P., Madara, J. C., Olson, D. P., Strochlic, D. E., Garfield, A. S., Vong, L., Pei, H., Watabe-Uchida, M., Uchida, N., et al. (2014) · Nature · doi:10.1038/nature12956 · Cited by 603 · see citing works
The arcuate nucleus as a conduit for diverse signals relevant to energy homeostasis
Cone, R. D., Cowley, M. A., Butler, A. A., Fan, W., Dl, M., & Low, M. J. (2001) · International Journal of Obesity · doi:10.1038/sj.ijo.0801913 · Cited by 591 · see citing works
Parallel, Redundant Circuit Organization for Homeostatic Control of Feeding Behavior
Betley, J. N., Cao, Z. F. H., Ritola, K., & Sternson, S. M. (2013) · Cell · doi:10.1016/j.cell.2013.11.002 · Cited by 591 · see citing works
Amygdala central nucleus lesions: Effect on heart rate conditioning in the rabbit
Kapp, B. S., Frysinger, R. C., Gallagher, M., & Haselton, J. R. (1979) · Physiology & Behavior · doi:10.1016/0031-9384(79)90304-4 · Cited by 590 · see citing works
Genetic identification of a neural circuit that suppresses appetite
Carter, M. E., Soden, M. E., Zweifel, L. S., & Palmiter, R. D. (2013) · Nature · doi:10.1038/nature12596 · Cited by 587 · see citing works
Activation of lateral habenula inputs to the ventral midbrain promotes behavioral avoidance
Stamatakis, A. M., & Stuber, G. D. (2012) · Nature Neuroscience · doi:10.1038/nn.3145 · Cited by 564 · see citing works
Self-citationTargeting cells with single vectors using multiple-feature Boolean logic
Fenno, L. E., Mattis, J., Ramakrishnan, C., Hyun, M., Lee, S. Y., He, M., Tucciarone, J., Selimbeyoglu, A., Berndt, A., Grosenick, L., et al. (2014) · Nature Methods · doi:10.1038/nmeth.2996 · Cited by 557 · see citing works
Visualizing Hypothalamic Network Dynamics for Appetitive and Consummatory Behaviors
Jennings, J. H., Ung, R. L., Resendez, S. L., Stamatakis, A. M., Taylor, J. G., Huang, J. H., Veleta, K., Kantak, P. A., Aita, M., Shilling-Scrivo, K. V., et al. (2015) · Cell · doi:10.1016/j.cell.2014.12.026 · Cited by 547 · see citing works
Self-citationDaily bingeing on sugar repeatedly releases dopamine in the accumbens shell
Rada, P. V., Avena, N. M., & Hoebel, B. G. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.04.043 · Cited by 542 · see citing works
Lateral hypothalamic circuits for feeding and reward
Stuber, G. D., & Wise, R. A. (2016) · Nature Neuroscience · doi:10.1038/nn.4220 · Cited by 519 · see citing works
Self-citationMidbrain dopamine neurons encode decisions for future action
Morris, G., Nevet, A., Arkadir, D., Vaadia, E., & Bergman, H. (2006) · Nature Neuroscience · doi:10.1038/nn1743 · Cited by 503 · see citing works
The Inhibitory Circuit Architecture of the Lateral Hypothalamus Orchestrates Feeding
Jennings, J. H., Rizzi, G., Stamatakis, A. M., Ung, R. L., & Stuber, G. D. (2013) · Science · doi:10.1126/science.1241812 · Cited by 493 · see citing works
Self-citationLeptin targets in the mouse brain
Scott, M. M., Lachey, J. L., Sternson, S. M., Lee, C. E., Elias, C. F., Friedman, J. M., & Elmquist, J. K. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.22025 · Cited by 484 · see citing works
Dorsal raphe neurons signal reward through 5-HT and glutamate
Liu, Z., Zhou, J., Li, Y., Hu, F., Lu, Y., Ma, M., Feng, Q., Zhang, J.-E., Wang, D., Zeng, J., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.010 · Cited by 469 · see citing works
Is dopamine a physiologically relevant mediator of feeding behavior?
Palmiter, R. D. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.06.004 · Cited by 469 · see citing works
Loss of GABAergic Signaling by AgRP Neurons to the Parabrachial Nucleus Leads to Starvation
Wu, Q., Boyle, M. P., & Palmiter, R. D. (2009) · Cell · doi:10.1016/j.cell.2009.04.022 · Cited by 465 · see citing works
Basolateral to Central Amygdala Neural Circuits for Appetitive Behaviors
Kim, J., Zhang, X., Muralidhar, S., LeBlanc, S., & Tonegawa, S. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.034 · Cited by 460 · see citing works
A whole-brain atlas of inputs to serotonergic neurons of the dorsal and median raphe nuclei
Pollak Dorocic, I., Fürth, D., Xuan, Y., Johansson, Y., Pozzi, L., Silberberg, G., Carlén, M., & Meletis, K. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.002 · Cited by 451 · see citing works
Oral sucrose stimulation increases accumbens dopamine in the rat
Hajnal, A., Smith, G. P., & Norgren, R. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00282.2003 · Cited by 449 · see citing works
Zhan, C., Zhou, J., Feng, Q., Zhang, J.-E., Lin, S., Bao, J., Wu, P., & Luo, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2742-12.2013 · Cited by 449 · see citing works
Paraventricular nucleus: A primary site mediating adrenergic stimulation of feeding and drinking
LEIBOWITZ, S. F. (1978) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(78)90333-7 · Cited by 439 · see citing works
A neural basis for melanocortin-4 receptor–regulated appetite
Garfield, A. S., Li, C., Madara, J. C., Shah, B. P., Webber, E. S., Steger, J. S., Campbell, J. N., Gavrilova, O., Lee, C. E., Olson, D. P., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4011 · Cited by 437 · see citing works
Arousal systems and attentional processes
Robbins, T. W. (1997) · Biological Psychology · doi:10.1016/s0301-0511(96)05222-2 · Cited by 430 · see citing works
Serotonergic control of the organization of feeding and satiety
Simansky, K. J. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(96)00066-6 · Cited by 427 · see citing works
Stachniak, T. J., Ghosh, A., & Sternson, S. M. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.008 · Cited by 427 · see citing works
Varela, L., & Horvath, T. L. (2012) · The EMBO Reports · doi:10.1038/embor.2012.174 · Cited by 426 · see citing works
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 421 · see citing works
Modulation of Brain Reward Circuitry by Leptin
Fulton, S. E., Woodside, B. C., & Shizgal, P. (2000) · Science · doi:10.1126/science.287.5450.125 · Cited by 421 · see citing works
Serotonin neurons in the dorsal raphe nucleus encode reward signals
Li, Y., Zhong, W., Wang, D., Feng, Q., Liu, Z., Zhou, J., Jia, C., Hu, F., Zeng, J., Guo, Q., et al. (2016) · Nature Communications · doi:10.1038/ncomms10503 · Cited by 420 · see citing works
Hill, J. M., Lesniak, M. A., Pert, C. B., & Roth, J. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90082-5 · Cited by 413 · see citing works
Leinninger, G. M., Jo, Y.-H., Leshan, R. L., Louis, G. W., Yang, H., Barrera, J. G., Wilson, H., Opland, D. M., Faouzi, M. A., Gong, Y., et al. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.06.011 · Cited by 412 · see citing works
AgRP(83-132) Acts as an Inverse Agonist on the Human-Melanocortin-4 Receptor
Nijenhuis, W. A. J., Oosterom, J., & Adan, R. A. H. (2001) · Molecular Endocrinology · doi:10.1210/mend.15.1.0578 · Cited by 408 · see citing works
Moga, M. M., Herbert, H., Hurley, K. M., Yasui, Y., Gray, T. S., & Saper, C. B. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902950408 · Cited by 407 · see citing works
Decoding Neural Circuits that Control Compulsive Sucrose Seeking
Nieh, E. H., Matthews, G. A., Allsop, S. A., Presbrey, K. N., Leppla, C. A., Wichmann, R., Neve, R., Wildes, C. P., & Tye, K. M. (2015) · Cell · doi:10.1016/j.cell.2015.01.003 · Cited by 402 · see citing works
Hypothalamic Control of Feeding and Self-Stimulation
Hoebel, B. G., & Teitelbaum, P. (1962) · Science · doi:10.1126/science.135.3501.375 · Cited by 389 · see citing works
Nieh, E. H., Vander Weele, C. M., Matthews, G. A., Presbrey, K. N., Wichmann, R., Leppla, C. A., Izadmehr, E. M., & Tye, K. M. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.035 · Cited by 387 · see citing works
Motivational activation: a unifying hypothesis of orexin/hypocretin function
Mahler, S. V., Moorman, D. E., Smith, R. J., James, M. H., & Aston‐Jones, G. (2014) · Nature Neuroscience · doi:10.1038/nn.3810 · Cited by 385 · see citing works
Bassareo, V., & Chiara, G. D. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-02-00851.1997 · Cited by 375 · see citing works
Central amygdala PKC-δ+ neurons mediate the influence of multiple anorexigenic signals
Cai, H., Haubensak, W. E., Anthony, T. E., & Anderson, D. J. (2014) · Nature Neuroscience · doi:10.1038/nn.3767 · Cited by 369 · see citing works
Deciphering a neuronal circuit that mediates appetite
Wu, Q., Clark, M. S., & Palmiter, R. D. (2012) · Nature · doi:10.1038/nature10899 · Cited by 359 · see citing works
Adamantidis, A. R., Tsai, H.-C., Boutrel, B., Zhang, F., Stuber, G. D., Budygin, E. A., Tourino, C., Bonci, A., Deisseroth, K., & de Lecea, L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2246-11.2011 · Cited by 357 · see citing works
Self-citationDopamine Production in the Caudate Putamen Restores Feeding in Dopamine-Deficient Mice
Szczypka, M. S., Kwok, K., Brot, M. D., Marck, B. T., Matsumoto, A. M., Donahue, B. A., & Palmiter, R. D. (2001) · Neuron · doi:10.1016/s0896-6273(01)00319-1 · Cited by 354 · see citing works
Real-time chemical responses in the nucleus accumbens differentiate rewarding and aversive stimuli
Roitman, M. F., Wheeler, R. A., Wightman, R. M., & Carelli, R. M. (2008) · Nature Neuroscience · doi:10.1038/nn.2219 · Cited by 343 · see citing works
Lu, J., Zhang, Y.-H., Chou, T. C., Gaus, S. E., Elmquist, J. K., Shiromani, P. J., & Saper, C. B. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-13-04864.2001 · Cited by 335 · see citing works
Castro, D. C., Cole, S. L., & Berridge, K. C. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00090 · Cited by 333 · see citing works
Identical "Feeding" and "Rewarding" Systems in the Lateral Hypothalamus of Rats
Margules, D. L., & Olds, J. (1962) · Science · doi:10.1126/science.135.3501.374 · Cited by 328 · see citing works
Stamatakis, A. M., van Swieten, M. M. H., Basiri, M. L., Blair, G. A., Kantak, P. A., & Stuber, G. D. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1202-15.2016 · Cited by 317 · see citing works
Self-citationAccumbal D1R Neurons Projecting to Lateral Hypothalamus Authorize Feeding
O’Connor, E. C., Kremer, Y., Lefort, S., Harada, M., Pascoli, V., Rohner, C., & Lüscher, C. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.038 · Cited by 308 · see citing works
Hunger-Driven Motivational State Competition
Burnett, C. J., Li, C., Webber, E., Tsaousidou, E., Xue, S. Y., Brüning, J. C., & Krashes, M. J. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.032 · Cited by 305 · see citing works
Muzerelle, A., Scotto-Lomassese, S., Bernard, J. F., Soiza-Reilly, M., & Gaspar, P. (2016) · Brain Structure and Function · doi:10.1007/s00429-014-0924-4 · Cited by 303 · see citing works
Whole-brain mapping of the direct inputs and axonal projections of POMC and AgRP neurons
Wang, D., He, X., Zhao, Z., Feng, Q., Lin, R., Sun, Y., Ding, T., Xu, F., Luo, M., & Zhan, C. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00040 · Cited by 298 · see citing works
Afferent connections to the bed nucleus of the stria terminalis
Weller, K. L., & Smith, D. A. (1982) · Brain Research · doi:10.1016/0006-8993(82)90272-4 · Cited by 293 · see citing works
Agouti-related peptide neural circuits mediate adaptive behaviors in the starved state
Padilla, S. L., Qiu, J., Soden, M. E., Sanz, E., Nestor, C. C., Barker, F. D., Quintana, A., Zweifel, L. S., Rønnekleiv, O. K., Kelly, M. J., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4274 · Cited by 293 · see citing works
Integrated Control of Predatory Hunting by the Central Nucleus of the Amygdala
Han, W., Téllez, L. A., Rangel, M. J., Motta, S. C., Zhang, X., Pérez-Martínez, I. O., Canteras, N. S., Shammah‐Lagnado, S. J., van den Pol, A. N., & de Araújo, I. E. (2017) · Cell · doi:10.1016/j.cell.2016.12.027 · Cited by 292 · see citing works
The Intrinsic Organization of the Central Extended Amygdala
Cassell, M. D., Freedman, L. J., & Shi, C. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09270.x · Cited by 287 · see citing works
Optogenetic Activation of Dorsal Raphe Serotonin Neurons Enhances Patience for Future Rewards
Miyazaki, K. W., Miyazaki, K., Tanaka, K. F., Yamanaka, A., Takahashi, A., Tabuchi, S., & Doya, K. (2014) · Current Biology · doi:10.1016/j.cub.2014.07.041 · Cited by 278 · see citing works
Rapid binge-like eating and body weight gain driven by zona incerta GABA neuron activation
Zhang, X., & van den Pol, A. N. (2017) · Science · doi:10.1126/science.aam7100 · Cited by 277 · see citing works
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 273 · see citing works
Hypothalamic Agrp Neurons Drive Stereotypic Behaviors beyond Feeding
Dietrich, M. O., Zimmer, M. R., Bober, J., & Horváth, T. L. (2015) · Cell · doi:10.1016/j.cell.2015.02.024 · Cited by 271 · see citing works
Corbett, D., & Wise, R. A. (1980) · Brain Research · doi:10.1016/0006-8993(80)90666-6 · Cited by 264 · see citing works
Aberman, J. E., & Salamone, J. D. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00004-4 · Cited by 263 · see citing works
Central amygdala circuits modulate food consumption through a positive-valence mechanism
Douglass, A. M., Kucukdereli, H., Ponserre, M., Marković, M., Gründemann, J., Strobel, C., Morales, P. L. A., Conzelmann, K., Lüthi, A., & Klein, R. (2017) · Nature Neuroscience · doi:10.1038/nn.4623 · Cited by 257 · see citing works
Similar roles of substantia nigra and ventral tegmental dopamine neurons in reward and aversion
Ilango, A., Kesner, A. J., Keller, K. L., Stuber, G. D., Bonci, A., & Ikemoto, S. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1703-13.2014 · Cited by 255 · see citing works
Serotonin manipulations and the structure of feeding behaviour
Blundell, J. E. (1986) · Appetite · doi:10.1016/s0195-6663(86)80051-4 · Cited by 251 · see citing works
Lesions of the hypothalamic paraventricular nucleus disrupt the initiation of maternal behavior
Insel, T. R., & Harbaugh, C. R. (1989) · Physiology & Behavior · doi:10.1016/0031-9384(89)90234-5 · Cited by 250 · see citing works
Organization of monosynaptic inputs to the serotonin and dopamine neuromodulatory systems
Ogawa, S. K., Cohen, J. Y., Hwang, D., Uchida, N., & Watabe-Uchida, M. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.042 · Cited by 249 · see citing works
A rapidly acting glutamatergic ARC→PVH satiety circuit postsynaptically regulated by α-MSH
Fenselau, H., Campbell, J. N., Verstegen, A. M. J., Madara, J. C., Xu, J., Shah, B. P., Resch, J. M., Yang, Z., Mandelblat-Cerf, Y., Livneh, Y., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4442 · Cited by 233 · see citing works
Leptin regulates the reward value of nutrient
Domingos, A. I., Vaynshteyn, J., Voss, H. U., Ren, X., Gradinaru, V., Zang, F., Deisseroth, K. A., de Araújo, I. E., & Friedman, J. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2977 · Cited by 230 · see citing works
Baldo, B. A., Sadeghian, K., Basso, A. M., & Kelley, A. E. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00293-0 · Cited by 228 · see citing works
Pothos, E. N., Creese, I., & Hoebel, B. G. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06640.1995 · Cited by 225 · see citing works
Lateral hypothalamic neuropeptides in reward and drug addiction
Dileone, R., Georgescu, D., & Nestler, E. J. (2003) · Life Sciences · doi:10.1016/s0024-3205(03)00408-9 · Cited by 220 · see citing works
Zhou, L., Sutton, G. M., Rochford, J. J., Semple, R. K., Lam, D. D., Oksanen, L., Thornton-Jones, Z. D., Clifton, P. G., Yueh, C.-Y., Evans, M. L., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.10.008 · Cited by 213 · see citing works
GABAergic and glutamatergic efferents of the mouse ventral tegmental area
Taylor, S. R., Badurek, S., Dileone, R., Nashmi, R., Minichiello, L., & Picciotto, M. R. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23603 · Cited by 209 · see citing works
Kapp, B. S., Gallagher, M., Underwood, M. D., McNall, C. L., & Whitehorn, D. (1982) · Brain Research · doi:10.1016/0006-8993(82)90866-6 · Cited by 208 · see citing works
Hypothalamic arcuate nucleus tyrosine hydroxylase neurons play orexigenic role in energy homeostasis
Zhang, X., & van den Pol, A. N. (2016) · Nature Neuroscience · doi:10.1038/nn.4372 · Cited by 205 · see citing works
Contributions of the hippocampus and medial prefrontal cortex to energy and body weight regulation
Davidson, T. L., Chan, K., Jarrard, L. E., Kanoski, S. E., Clegg, D. J., & Benoit, S. C. (2008) · Hippocampus · doi:10.1002/hipo.20499 · Cited by 204 · see citing works
Hnasko, T. S., Perez, F. A., Scouras, A. D., Stoll, E. A., Gale, S. D., Luquet, S. H., Phillips, P. E. M., Kremer, E. J., & Palmiter, R. D. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603081103 · Cited by 198 · see citing works
Hunger neurons drive feeding through a sustained, positive reinforcement signal.
Chen, Y., Lin, Y.-C., Zimmerman, C. A., Essner, R. A., & Knight, Z. A. (2016) · eLife · doi:10.7554/elife.18640 · Cited by 196 · see citing works
Neurophysiological analysis of brain-stimulation reward in the monkey
Rolls, E. T., Burton, M. J., & Mora, F. (1980) · Brain Research · doi:10.1016/0006-8993(80)91216-0 · Cited by 193 · see citing works
Ghrelin Acts as an Interface between Physiological State and Phasic Dopamine Signaling
Cone, J. J., McCutcheon, J. E., & Roitman, M. F. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4404-13.2014 · Cited by 185 · see citing works
Plasma corticosterone responses to electrical stimulation of the bed nucleus of the stria terminalis
Dunn, J. D. (1987) · Brain Research · doi:10.1016/0006-8993(87)91111-5 · Cited by 184 · see citing works
Medial prefrontal D1 dopamine neurons control food intake
Land, B. B., Narayanan, N. S., Liu, R.-J., Gianessi, C. A., Brayton, C. E., Grimaldi, D. M., Sarhan, M., Guarnieri, D. J., Deisseroth, K. A., Aghajanian, G. K., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3625 · Cited by 180 · see citing works
Palatability Can Drive Feeding Independent of AgRP Neurons
Denis, R. G. P., Joly-Amado, A., Webber, E., Langlet, F., Schaeffer, M., Padilla, S. L., Cansell, C., Dehouck, B., Castel, J., Delbès, A.-S., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.07.011 · Cited by 164 · see citing works
AgRP neurons regulate development of dopamine neuronal plasticity and nonfood-associated behaviors
Dietrich, M. O., Bober, J., Ferreira, J. G., Tellez, L. A., Mineur, Y. S., Souza, D. O., Gao, X.-B., Picciotto, M. R., Araújo, I., Liu, Z.-W., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3147 · Cited by 158 · see citing works
Inhibitory Interplay between Orexin Neurons and Eating
González, J. A., Jensen, L. T., Ιορδανίδου, Π., Strom, M., Fugger, L. H., & Burdakov, D. (2016) · Current Biology · doi:10.1016/j.cub.2016.07.013 · Cited by 155 · see citing works
Hypothalamic melanin concentrating hormone neurons communicate the nutrient value of sugar
Domingos, A. I., Sordillo, A., Dietrich, M. O., Liu, Z.-W., Téllez, L. A., Vaynshteyn, J., Ferreira, J. G. P., Ekstrand, M. I., Horváth, T. L., de Araújo, I. E., et al. (2013) · eLife · doi:10.7554/elife.01462 · Cited by 154 · see citing works
Danjo, T., Yoshimi, K., Funabiki, K., Yawata, S., & Nakanishi, S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1404323111 · Cited by 153 · see citing works
Cancer-induced anorexia and malaise are mediated by CGRP neurons in the parabrachial nucleus
Campos, C., Bowen, A. J., Han, S., Wisse, B. E., Palmiter, R. D., & Schwartz, M. W. (2017) · Nature Neuroscience · doi:10.1038/nn.4574 · Cited by 150 · see citing works
c-Fos induction in response to a conditioned stimulus after single trial taste aversion learning
Swank, M. W., & Bernstein, I. L. (1994) · Brain Research · doi:10.1016/0006-8993(94)91018-9 · Cited by 140 · see citing works
Projections of the Parabrachial Nucleus in the Old World Monkey
Pritchard, T. C., Hamilton, R. B., & Norgren, R. (2000) · Experimental Neurology · doi:10.1006/exnr.2000.7450 · Cited by 134 · see citing works
Reilly, S., Grigson, P. S., & Norgren, R. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.6.1005 · Cited by 132 · see citing works
Stamatakis, A. M., Sparta, D. R., Jennings, J. H., McElligott, Z. A., Decot, H., & Stuber, G. D. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.046 · Cited by 132 · see citing works
Self-citationHammack, S. E., Richey, K. J., Watkins, L. R., & Maier, S. F. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.2.443 · Cited by 130 · see citing works
Sharpe, M. J., Marchant, N. J., Ramsey, L. A., Richie, C. T., Zhang, Y. J., Campbell, E. J., Koivula, P. P., Necarsulmer, J., Mejías-Aponte, C. A., Morales, M., et al. (2017) · Current Biology · doi:10.1016/j.cub.2017.06.024 · Cited by 129 · see citing works
Casada, J. H., & Dafny, N. (1991) · Brain Research Bulletin · doi:10.1016/0361-9230(91)90069-v · Cited by 128 · see citing works
Gordh, A. S., & Berridge, K. C. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02691-3 · Cited by 128 · see citing works
Concurrent and robust regulation of feeding behaviors and metabolism by orexin neurons
Inutsuka, A., Inui, A., Tabuchi, S., Tsunematsu, T., Lazarus, M., & Yamanaka, A. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.06.015 · Cited by 126 · see citing works
Optogenetic activation of serotonergic neurons enhances anxiety-like behaviour in mice
Ohmura, Y., Tanaka, K. F., Tsunematsu, T., Yamanaka, A., & Yoshioka, M. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145714000637 · Cited by 122 · see citing works
Qualls‐Creekmore, E., Yu, S., Francois, M., Hoang, J. G., Huesing, C., Bruce‐Keller, A. J., Burk, D. H., Berthoud, H., Morrison, C. D., & Münzberg, H. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0155-17.2017 · Cited by 121 · see citing works
Operant self-stimulation of dopamine neurons in the substantia nigra
Rossi, M. A., Sukharnikova, T., Hayrapetyan, V. Y., Yang, L., & Yin, H. H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065799 · Cited by 119 · see citing works
Self-citationAntipsychotic drug-induced weight gain: development of an animal model
Cope, M. B., Nagy, T. R., Fernández, J. R., Geary, N., Casey, D. E., & Allison, D. B. (2005) · International Journal of Obesity · doi:10.1038/sj.ijo.0802928 · Cited by 114 · see citing works
Reilly, S., Grigson, P. S., & Norgren, R. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.6.1005 · Cited by 112 · see citing works
Prefrontal cortex and the regulation of food intake in the rat.
Kolb, B. E., & Nonneman, A. J. (1975) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0076397 · Cited by 107 · see citing works
Feeding can enhance dopamine turnover in the prefrontal cortex
Hernandez, L., & Hoebel, B. G. (1990) · Brain Research Bulletin · doi:10.1016/0361-9230(90)90197-8 · Cited by 107 · see citing works
Male and female 5-HT1B receptor knockout mice have higher body weights than wildtypes
Bouwknecht, J. A., van der Gugten, J., Hijzen, T. H., Maes, R. A. A., Hen, R., & Olivier, B. (2001) · Physiology & Behavior · doi:10.1016/s0031-9384(01)00589-3 · Cited by 106 · see citing works
Neuropeptide Regulation of Signaling and Behavior in the BNST
Kash, T. L., Pleil, K. E., Marcinkiewcz, C. A., Lowery‐Gionta, E. G., Crowley, N. A., Mazzone, C. M., Sugam, J. A., Hardaway, J. A., & McElligott, Z. A. (2014) · Molecules and Cells · doi:10.14348/molcells.2015.2261 · Cited by 105 · see citing works
Navarro, M., Olney, J. J., Burnham, N. W., Mazzone, C. M., Lowery‐Gionta, E. G., Pleil, K. E., Kash, T. L., & Thiele, T. E. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.304 · Cited by 103 · see citing works
Gs-coupled GPCR signalling in AgRP neurons triggers sustained increase in food intake
Nakajima, K., Cui, Z., Li, C., Meister, J., Cui, Y., Fu, O., Smith, A. S., Jain, S., Lowell, B. B., Krashes, M. J., et al. (2016) · Nature Communications · doi:10.1038/ncomms10268 · Cited by 102 · see citing works
Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
Laque, A., Yu, S., Qualls‐Creekmore, E., Gettys, S., Schwartzenburg, C., Bui, K., Rhodes, C. J., Berthoud, H., Morrison, C. D., Richards, B. K. S., et al. (2015) · Molecular Metabolism · doi:10.1016/j.molmet.2015.07.002 · Cited by 99 · see citing works
Wu, Z., Kim, E. R., Sun, H., Xu, Y., Mangieri, L. R., Li, D., Pan, H., Xu, Y., Arenkiel, B. R., & Tong, Q. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3720-14.2015 · Cited by 95 · see citing works
Optogenetic activation of brainstem serotonergic neurons induces persistent pain sensitization
Cai, Y.-Q., Wang, W., Hou, Y.-Y., & Pan, Z.-Z. Z. (2014) · Molecular Pain · doi:10.1186/1744-8069-10-70 · Cited by 94 · see citing works
Li, C., Cho, Y. K., & Smith, D. V. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00828.2004 · Cited by 88 · see citing works
Striatal Dopamine Links Gastrointestinal Rerouting to Altered Sweet Appetite
Han, W., Téllez, L. A., Niu, J., Medina, S., Ferreira, T. L., Zhang, X., Su, J., Tong, J., Schwartz, G. J., van den Pol, A. N., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.10.009 · Cited by 84 · see citing works
Coizet, V., Dommett, E. J., Klop, E. M., Redgrave, P., & Overton, P. G. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.03.049 · Cited by 80 · see citing works
Carr, K. D., & Wolinsky, T. D. (1993) · Brain Research · doi:10.1016/0006-8993(93)91499-i · Cited by 78 · see citing works
Robinson, S., Rainwater, A., Hnasko, T. S., & Palmiter, R. D. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0579-9 · Cited by 77 · see citing works
Kask, A., & Schiöth, H. B. (2000) · Brain Research · doi:10.1016/s0006-8993(00)03034-1 · Cited by 70 · see citing works
Regulation of feline aggression by the bed nucleus of stria terminalis
Shaikh, M. B., Brutus, M., Siegel, H. E., & Siegel, A. (1986) · Brain Research Bulletin · doi:10.1016/0361-9230(86)90031-6 · Cited by 69 · see citing works
Potentiation of reward by hunger is opioid mediated
Carr, K. D., & Simon, E. J. (1984) · Brain Research · doi:10.1016/0006-8993(84)90578-x · Cited by 63 · see citing works
Dopamine dependency for acquisition and performance of Pavlovian conditioned response
Darvas, M., Wunsch, A. M., Gibbs, J. T., & Palmiter, R. D. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400332111 · Cited by 59 · see citing works
Abrahamsen, G. C., Berman, Y. L., & Carr, K. D. (1995) · Brain Research · doi:10.1016/0006-8993(95)00764-h · Cited by 56 · see citing works
Alkemade, A., Yi, C., Pei, L., Harakaľová, M., Swaab, D. F., la Fleur, S. E., Fliers, E., & Kalsbeek, A. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-3259 · Cited by 54 · see citing works
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 52 · see citing works
Self-stimulation of the lateral hypothalamus modified by insulin and glucagon☆
Balagura, S., & Hoebel, B. G. (1967) · Physiology & Behavior · doi:10.1016/0031-9384(67)90048-0 · Cited by 37 · see citing works
Synaptic Plasticity in the Central Nucleus of the Amygdala
Samson, R. D., Duvarci, S., & Paré, D. (2005) · Reviews in the Neurosciences · doi:10.1515/revneuro.2005.16.4.287 · Cited by 36 · see citing works
Patterns of fos activation in rat raphe nuclei during feeding behavior
Takase, L. F., & Nogueira, M. I. (2008) · Brain Research · doi:10.1016/j.brainres.2008.01.036 · Cited by 31 · see citing works
Involvement of CRF2 receptor in the brain regions in restraint-induced anorexia
Ohata, H., & Shibasaki, T. (2011) · Neuroreport · doi:10.1097/wnr.0b013e3283487467 · Cited by 30 · see citing works
Paraventricular Nucleus Sim1 Neuron Ablation Mediated Obesity Is Resistant to High Fat Diet
Dong, X., Roizen, J. D., Lai, M., Gandhi, N. M., & Kublaoui, B. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081087 · Cited by 14 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Neural mechanisms of social homeostasis
Matthews, G. A., & Tye, K. M. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14016 · Cited by 273 · see citing works
Arcuate Nucleus-Dependent Regulation of Metabolism—Pathways to Obesity and Diabetes Mellitus
Jaïs, A., & Brüning, J. C. (2021) · Endocrine Reviews · doi:10.1210/endrev/bnab025 · Cited by 282 · see citing works
de Araújo, I. E., Schatzker, M., & Small, D. M. (2019) · Annual Review of Psychology · doi:10.1146/annurev-psych-122216-011643 · Cited by 262 · see citing works
Brain–gut–microbiome interactions in obesity and food addiction
Gupta, A., Osadchiy, V., & Mayer, E. A. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-0341-5 · Cited by 268 · see citing works
Obesity I: Overview and molecular and biochemical mechanisms
Lustig, R. H., Collier, D., Kassotis, C., Roepke, T. A., Kim, M. J., Blanc, E., Barouki, R., Bansal, A., Cave, M. C., Chatterjee, S., et al. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.115012 · Cited by 203 · see citing works
Central regulation of food intake in fish: an evolutionary perspective
Soengas, J. L., Cerdá‐Reverter, J. M., & Delgado, M. J. (2018) · Journal of Molecular Endocrinology · doi:10.1530/jme-17-0320 · Cited by 165 · see citing works
Obesity remodels activity and transcriptional state of a lateral hypothalamic brake on feeding
Rossi, M. A., Basiri, M. L., McHenry, J. A., Kosyk, O., Otis, J. M., van den Munkhof, H. E., Bryois, J., Hübel, C., Breen, G. D., Guo, W., et al. (2019) · Science · doi:10.1126/science.aax1184 · Cited by 164 · see citing works
Self-citationCentral nervous system regulation of organismal energy and glucose homeostasis
Myers, M. G., Affinati, A. H., Richardson, N. E., & Schwartz, M. W. (2021) · Nature Metabolism · doi:10.1038/s42255-021-00408-5 · Cited by 154 · see citing works
Genetics and neurobiology of eating disorders
Bulik, C. M., Coleman, J. R. I., Hardaway, J. A., Breithaupt, L. E., Watson, H. J., Bryant, C. D., & Breen, G. D. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01071-z · Cited by 154 · see citing works
Neural Control and Modulation of Thirst, Sodium Appetite, and Hunger
Augustine, V., Lee, S., & Oka, Y. (2020) · Cell · doi:10.1016/j.cell.2019.11.040 · Cited by 135 · see citing works
Microbiota‐gut‐brain axis as a regulator of reward processes
García‐Cabrerizo, R., Carbia, C., O’Riordan, K. J., Schellekens, H., & Cryan, J. F. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15284 · Cited by 147 · see citing works
Dopamine subsystems that track internal states
Grove, J. C. R., Gray, L. A., Medina, N. L. S., Sivakumar, N., Ahn, J. S., Corpuz, T. V., Berke, J. D., Kreitzer, A. C., & Knight, Z. A. (2022) · Nature · doi:10.1038/s41586-022-04954-0 · Cited by 145 · see citing works
Reverse-translational identification of a cerebellar satiation network
Low, A. Y. T., Goldstein, N., Gaunt, J. R., Huang, K.-P., Zainolabidin, N., Yip, A. K. K., Carty, J. R. E., Choi, J. Y., Miller, A. M., Ho, H. S. T., et al. (2021) · Nature · doi:10.1038/s41586-021-04143-5 · Cited by 135 · see citing works
Alhadeff, A. L., Goldstein, N., Park, O., Klima, M. L., Vargas, A. P.-D., & Betley, J. N. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.050 · Cited by 138 · see citing works
Brain functional and structural magnetic resonance imaging of obesity and weight loss interventions
Li, G., Hu, Y., Zhang, W., Wang, J., Ji, W., Manza, P., Volkow, N. D., Zhang, Y., & Wang, G. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02025-y · Cited by 135 · see citing works
A Farewell to Art: Aesthetics as a Topic in Psychology and Neuroscience
Skov, M., & Nadal, M. (2020) · Perspectives on Psychological Science · doi:10.1177/1745691619897963 · Cited by 120 · see citing works
Krolick, K. N., Zhu, Q., & Shi, H. (2018) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2018.07.008 · Cited by 121 · see citing works
Amygdala NPY Circuits Promote the Development of Accelerated Obesity under Chronic Stress Conditions
Ip, C. K., Zhang, L., Farzi, A., Qi, Y., Clarke, I. M., Reed, F. M., Shi, Y., Enriquez, R. F., Dayas, C. V., Graham, B. A., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.04.001 · Cited by 112 · see citing works
Campos, A., Port, J. D., & Acosta, A. J. (2022) · Brain Sciences · doi:10.3390/brainsci12040431 · Cited by 115 · see citing works
Qiu, J., Rivera, H. M., Bosch, M. A., Padilla, S. L., Stincic, T. L., Palmiter, R. D., Kelly, M. J., & Rønnekleiv, O. K. (2018) · eLife · doi:10.7554/elife.35656 · Cited by 114 · see citing works
Ultra-Processed Food, Reward System and Childhood Obesity
Calcaterra, V., Cena, H., Rossi, V., Santero, S., Bianchi, A., & Zuccotti, G. (2023) · Children · doi:10.3390/children10050804 · Cited by 114 · see citing works
An insula hierarchical network architecture for active interoceptive inference
Fermin, A. S. R., Friston, K., & Yamawaki, S. (2022) · Royal Society Open Science · doi:10.1098/rsos.220226 · Cited by 101 · see citing works
FGF21 and the physiological regulation of macronutrient preference
Hill, C. M., Qualls-Creekmore, E., Berthoud, H.-R., Soto, P., Yu, S., McDougal, D. H., Münzberg, H., & Morrison, C. D. (2020) · Endocrinology · doi:10.1210/endocr/bqaa019 · Cited by 99 · see citing works
Zhang, J., Chen, D., Sweeney, P. R., & Yang, Y. (2020) · Nature Communications · doi:10.1038/s41467-020-20093-4 · Cited by 97 · see citing works
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 96 · see citing works
Gaspar, J. M., & Velloso, L. A. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00813 · Cited by 94 · see citing works
Anatomy and Function of Ventral Tegmental Area Glutamate Neurons
Cai, J., & Tong, Q. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.867053 · Cited by 89 · see citing works
Glucocorticoids, stress and eating: The mediating role of appetite‐regulating hormones
Kuckuck, S., van der Valk, E. S., Scheurink, A. J. W., van der Voorn, B., Iyer, A. M., Visser, J. A., Delhanty, P. J. D., van den Berg, S. A. A., & van Rossum, E. F. C. (2022) · Obesity Reviews · doi:10.1111/obr.13539 · Cited by 94 · see citing works
Fish as models for understanding the vertebrate endocrine regulation of feeding and weight
Volkoff, H. (2019) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2019.04.017 · Cited by 86 · see citing works
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 82 · see citing works
Rossi, M. A., Basiri, M. L., Liu, Y., Hashikawa, Y., Hashikawa, K., Fenno, L. E., Kim, Y. S., Ramakrishnan, C., Deisseroth, K. A., & Stuber, G. D. (2021) · Neuron · doi:10.1016/j.neuron.2021.09.020 · Cited by 72 · see citing works
Self-citationConsequences of Obesity on the Sense of Taste: Taste Buds as Treatment Targets?
Rohde, K., Schamarek, I., & Blüher, M. (2020) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2020.0058 · Cited by 74 · see citing works
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 73 · see citing works
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 68 · see citing works
Qi, Y., Lee, N. J., Ip, C. K., Enriquez, R. F., Tasan, R. O., Zhang, L., & Herzog, H. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.04.020 · Cited by 67 · see citing works
van Galen, K. A., Schrantee, A., ter Horst, K. W., la Fleur, S. E., Booij, J., Constable, R. T., Schwartz, G. J., Dileone, R., & Serlie, M. J. M. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00816-9 · Cited by 65 · see citing works
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 · see citing works
Eating disorders and obesity: bridging clinical, neurobiological, and therapeutic perspectives
Camacho‐Barcia, L., Giel, K. E., Jiménez‐Múrcia, S., Álvarez‐Pitti, J., Micali, N., Lucas, I., Miranda‐Olivos, R., Munguía, L., Tena‐Sempere, M., Zipfel, S., et al. (2024) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2024.02.007 · Cited by 63 · see citing works
A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding
Chen, Z., Chen, G., Zhong, J., Jiang, S., Lai, S., Xu, H. Z., Deng, X., Li, F., Lu, S., Zhou, K., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01742-0 · Cited by 60 · see citing works
Metabolic and feeding adjustments during pregnancy
Haddad-Tóvolli, R., & Claret, M. (2023) · Nature Reviews Endocrinology · doi:10.1038/s41574-023-00871-y · Cited by 58 · see citing works
Konanur, V., Hsu, T. M., Kanoski, S. E., Hayes, M. R., & Roitman, M. F. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.112771 · Cited by 58 · see citing works
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 57 · see citing works
Sulforaphane reduces obesity by reversing leptin resistance
Çakır, I., Pan, P. L., Hadley, C. K., El-Gamal, A., Fadel, A., Elsayegh, D., Mohamed, O., Rizk, N. M., & Ghamari‐Langroudi, M. (2022) · eLife · doi:10.7554/elife.67368 · Cited by 55 · see citing works
Gut microbiota suppress feeding induced by palatable foods
Ousey, J. A., Boktor, J. C., & Mazmanian, S. K. (2022) · Current Biology · doi:10.1016/j.cub.2022.10.066 · Cited by 56 · see citing works
Deep Brain Stimulation for Obesity: A Review and Future Directions
Formolo, D. A., Gaspar, J. M., Melo, H. M., Eichwald, T., Zepeda, R. J., Latini, A., Okun, M. S., & Walz, R. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00323 · Cited by 56 · see citing works
Naneix, F., Peters, K. Z., & McCutcheon, J. E. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.10.036 · Cited by 55 · see citing works
Rainbow trout prefer diets rich in omega-3 long chain polyunsaturated fatty acids DHA and EPA
Roy, J., Mercier, Y., Tonnet, L., Burel, C., Lanuque, A., Surget, A., Larroquet, L., Corraze, G. R., Terrier, F., Panserat, S., et al. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.112692 · Cited by 53 · see citing works
Ovarian Hormones and Reward Processes in Palatable Food Intake and Binge Eating
Ma, R., Mikhail, M. E., Culbert, K. M., Johnson, A. W., Sisk, C. L., & Klump, K. L. (2019) · Physiology · doi:10.1152/physiol.00013.2019 · Cited by 55 · see citing works
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 · see citing works
Homeostatic medicine: a strategy for exploring health and disease
Wang, S., & Qin, L. (2022) · Current Medicine · doi:10.1007/s44194-022-00016-9 · Cited by 56 · see citing works
Yuan, F., Jiang, H., Yin, H., Jiang, X., Jiao, F., Chen, S., Ying, H., Chen, Y., Zhai, Q., & Guo, F. (2020) · Nature Communications · doi:10.1038/s41467-020-16662-2 · Cited by 51 · see citing works
Control of energy homeostasis by the lateral hypothalamic area
Rossi, M. A. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.05.010 · Cited by 50 · see citing works
Self-citationThirst recruits phasic dopamine signaling through subfornical organ neurons
Hsu, T. M., Bazzino, P., Hurh, S. J., Konanur, V., Roitman, J. D., & Roitman, M. F. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2009233117 · Cited by 50 · see citing works
Grippo, R. M., Tang, Q., Zhang, Q., Chadwick, S. R., Gao, Y., Altherr, E. B., Sipe, L. M., Purohit, A. M., Purohit, N. M., Sunkara, M., et al. (2020) · Current Biology · doi:10.1016/j.cub.2019.11.029 · Cited by 49 · see citing works
Consensus Paper: Cerebellum and Reward
Manto, M. U., Adamaszek, M., Apps, R., Carlson, E. S., Guarque‐Chabrera, J., Heleven, E., Kakei, S., Khodakhah, K., Kuo, S., Lin, C.-Y. R., et al. (2024) · The Cerebellum · doi:10.1007/s12311-024-01702-0 · Cited by 50 · see citing works
Top-down control of conditioned overconsumption is mediated by insular cortex Nos1 neurons
Stern, S. A., Azevedo, E. P., Pomeranz, L. E., Doerig, K. R., Ivan, V. J., & Friedman, J. M. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.03.001 · Cited by 47 · see citing works
The neurobiology of overeating
Stuber, G. D., Schwitzgebel, V., & Lüscher, C. (2025) · Neuron · doi:10.1016/j.neuron.2025.03.010 · Cited by 48 · see citing works
Self-citationPhua, S. C., Tan, Y. L., Kok, A. M. Y., Senol, E., Chiam, C. J. H., Lee, C.-Y., Peng, Y., Lim, A. T. J., Mohammad, H., Lim, J.-X., et al. (2021) · Science Advances · doi:10.1126/sciadv.abe4323 · Cited by 47 · see citing works
Endocannabinoids in Body Weight Control
Horn, H., Böhme, B., Dietrich, L., & Koch, M. (2018) · Pharmaceuticals · doi:10.3390/ph11020055 · Cited by 46 · see citing works
Modulation of Feeding and Associated Behaviors by Lateral Hypothalamic Circuits
Qualls‐Creekmore, E., & Münzberg, H. (2018) · Endocrinology · doi:10.1210/en.2018-00449 · Cited by 42 · see citing works
The partial inhibition of hypothalamic IRX3 exacerbates obesity
de Araújo, T. M., Razolli, D. S., Corrêa‐da‐Silva, F., Júnior, J. C. D. L., Gaspar, R. S., Sidarta-Oliveira, D., Victorio, S. C. D. S., Donato, J., Kim, Y., & Velloso, L. A. (2018) · EBioMedicine · doi:10.1016/j.ebiom.2018.11.048 · Cited by 46 · see citing works
The Insula Cortex Contacts Distinct Output Streams of the Central Amygdala
Ponserre, M., Peters, C., Fermani, F., Conzelmann, K., & Klein, R. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0567-20.2020 · Cited by 43 · see citing works
Chakravarthy, V. S., Balasubramani, P. P., Mandali, A., Jahanshahi, M., & Moustafa, A. A. (2018) · Physiology & Behavior · doi:10.1016/j.physbeh.2018.06.032 · Cited by 43 · see citing works
Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology
Maynard, T. M., Zohn, I. E., Moody, S. A., & LaMantia, A. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100419-100636 · Cited by 44 · see citing works
Internal-state-dependent control of feeding behavior via hippocampal ghrelin signaling
Wee, R. W. S., Mishchanchuk, K., AlSubaie, R., Church, T. W., Gold, M. G., & MacAskill, A. F. (2023) · Neuron · doi:10.1016/j.neuron.2023.10.016 · Cited by 50 · see citing works
Molecular Alterations of the Endocannabinoid System in Psychiatric Disorders
Navarro, D., Gasparyan, A., Navarrete, F., Torregrosa, A. B., Rubio, G., Marín, M., Acosta, G. B., García‐Gutiérrez, M. S., & Manzanares, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094764 · Cited by 45 · see citing works
Skov, M., & Nadal, M. (2019) · Psychology of Aesthetics Creativity and the Arts · doi:10.1037/aca0000278 · Cited by 40 · see citing works
Astrocytes in neuroendocrine systems: An overview
MacDonald, A. J., Robb, J. L., Morrissey, N. A., Beall, C., & Ellacott, K. L. J. (2019) · Journal of Neuroendocrinology · doi:10.1111/jne.12726 · Cited by 38 · see citing works
Morales, I. (2022) · Appetite · doi:10.1016/j.appet.2022.106146 · Cited by 39 · see citing works
Fang, X., Chen, Y., Wang, J., Zhang, Z., Bai, Y., Denney, K., Gan, L., Guo, M., Weintraub, N. L., Lei, Y., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01872-5 · Cited by 37 · see citing works
The cognitive (lateral) hypothalamus
Sharpe, M. J. (2023) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2023.08.019 · Cited by 38 · see citing works
Nicotine' actions on energy balance: Friend or foe?
Seoane-Collazo, P., Diéguez, C., Nogueiras, R., Rahmouni, K., Fernández-Real, J., & López, M. (2020) · Pharmacology and Therapeutics · doi:10.1016/j.pharmthera.2020.107693 · Cited by 38 · see citing works
López-Muciño, L. A., García‐García, F., Cueto‐Escobedo, J., Acosta-Hernández, M. E., Venebra-Muñoz, A., & Rodríguez‐Alba, J. C. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104832 · Cited by 39 · see citing works
Gut-to-brain signals in feeding control
Moura‐Assis, A., Friedman, J. M., & Velloso, L. A. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00388.2020 · Cited by 38 · see citing works
Astrocyte Gliotransmission in the Regulation of Systemic Metabolism
Murat, C. D. B., & García‐Cáceres, C. (2021) · Metabolites · doi:10.3390/metabo11110732 · Cited by 36 · see citing works
Neural circuit control of innate behaviors
Wei, X., Jiao, Z., Senol, E., Yao, J., Zhao, M., Zhao, Z., Chen, X., Cao, P., Fu, Y., Gao, Z., et al. (2021) · Science China Life Sciences · doi:10.1007/s11427-021-2043-2 · Cited by 38 · see citing works
Seeking the Psilocybiome: Psychedelics meet the microbiota-gut-brain axis
Kelly, J. R., Clarke, G. A., Harkin, A., Corr, S. C., Galvin, S. D., Pradeep, V., Cryan, J. F., O’Keane, V., & Dinan, T. G. (2022) · International Journal of Clinical and Health Psychology · doi:10.1016/j.ijchp.2022.100349 · Cited by 38 · see citing works
Comesaña, S., Velasco, C., Conde‐Sieira, M., Míguez, J. M., Soengas, J. L., & Morais, S. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01209 · Cited by 36 · see citing works
Control-theory models of body-weight regulation and body-weight-regulatory appetite
Geary, N. (2019) · Appetite · doi:10.1016/j.appet.2019.104440 · Cited by 36 · see citing works
Interleukin-17 acts in the hypothalamus reducing food intake
Nogueira, G. A. S., Solon, C., Carraro, R. S., Engel, D. F., Ramalho, A. F. S., Sidarta-Oliveira, D., Gaspar, R. S., Bombassaro, B., Vasques, A. C. J., Geloneze, B., et al. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.12.012 · Cited by 41 · see citing works
Taste of Fat and Obesity: Different Hypotheses and Our Point of View
Brondel, L., Quilliot, D., Mouillot, T., Khan, N. A., Bastable, P., Boggio, V., Leloup, C., & Pénicaud, L. (2022) · Nutrients · doi:10.3390/nu14030555 · Cited by 36 · see citing works
Rezitis, J., Herzog, H., & Ip, C. K. (2021) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2021.110449 · Cited by 35 · see citing works
O-GlcNAc cycling in the developing, adult and geriatric brain
Lagerlöf, O. (2018) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-018-9760-1 · Cited by 35 · see citing works
An open-source platform for head-fixed operant and consummatory behavior
Gordon-Fennell, A., Barbakh, J. M., Utley, M. T., Singh, S., Bazzino, P., Gowrishankar, R., Bruchas, M. R., Roitman, M. F., & Stuber, G. D. (2023) · eLife · doi:10.7554/elife.86183 · Cited by 34 · see citing works
Self-citationAltherr, E. B., Rainwater, A., Kaviani, D., Tang, Q., & Güler, A. D. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113470 · Cited by 33 · see citing works
Boswell, N., Byrne, R., & Davies, P. S. W. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.10.020 · Cited by 33 · see citing works
Sun‐Waterhouse, D., Kang, W., Ma, C., & Waterhouse, G. I. N. (2021) · Journal of Future Foods · doi:10.1016/j.jfutfo.2021.09.001 · Cited by 33 · see citing works
Translational models of stress and resilience: An applied neuroscience methodology review
Albayrak, Z. S., Vaz, A., Bordes, J., Ünlü, S., Sep, M. S. C., Vinkers, C. H., Pinto, L., & Eser, H. Y. (2024) · Neuroscience Applied · doi:10.1016/j.nsa.2024.104064 · Cited by 39 · see citing works
Neurotensin neurons in the extended amygdala control dietary choice and energy homeostasis
Furlan, A., Corona, A., Boyle, S., Sharma, R., Rubino, R., Habel, J., Gablenz, E., Giovanniello, J. R., Beyaz, S., Janowitz, T., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01178-3 · Cited by 32 · see citing works
Transcriptomics reveals amygdala neuron regulation by fasting and ghrelin thereby promoting feeding
Peters, C., He, S., Fermani, F., Lim, H., Ding, W., Mayer, C., & Klein, R. (2023) · Science Advances · doi:10.1126/sciadv.adf6521 · Cited by 29 · see citing works
Feed Intake Regulation in Fish: Implications for Aquaculture
Soengas, J. L., Comesaña, S., Blanco, A. M., & Conde‐Sieira, M. (2024) · Reviews in Fisheries Science & Aquaculture · doi:10.1080/23308249.2024.2374259 · Cited by 31 · see citing works
Fortin, S. M., & Roitman, M. F. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0399-18.2018 · Cited by 30 · see citing works
Salem, V., Demetriou, L., Behary, P., Αλεξιάδου, Κ., Scholtz, S., Tharakan, G., Miras, A. D., Purkayastha, S., Ahmed, A. R., Bloom, S. R., et al. (2021) · Diabetes Care · doi:10.2337/dc20-2641 · Cited by 31 · see citing works
Xiphoid nucleus of the midline thalamus controls cold-induced food seeking
Lal, N. K., Le, P., Aggarwal, S., Zhang, A., Wang, K., Qi, T., Pang, Z., Yang, D., Nudell, V., Yeo, G. W.-M., et al. (2023) · Nature · doi:10.1038/s41586-023-06430-9 · Cited by 30 · see citing works
Mechanisms Mediating the Actions of Fatty Acids in the Hypothalamus
Dragano, N. R. V., Monfort‐Pires, M., & Velloso, L. A. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.10.012 · Cited by 30 · see citing works
Recent Advances in Neural Circuits for Taste Perception in Hunger
Fu, O., Minokoshi, Y., & Nakajima, K. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.609824 · Cited by 30 · see citing works
Brown, R. M., & James, M. H. (2023) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2023.110717 · Cited by 30 · see citing works
Kim, S.-R., & Kim, S. (2021) · Molecules and Cells · doi:10.14348/molcells.2021.0006 · Cited by 29 · see citing works
Peripheral and Central Nutrient Sensing Underlying Appetite Regulation
Augustine, V., Gökçe, S. K., & Oka, Y. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.05.003 · Cited by 29 · see citing works
Activation of GPR40 induces hypothalamic neurogenesis through p38- and BDNF-dependent mechanisms
Engel, D. F., Bóbbo, V. C. D., Solon, C., Nogueira, G. A. S., Moura‐Assis, A., Mendes, N. F., Zanesco, A. M., Papangelis, A., Ulven, T., & Velloso, L. A. (2020) · Scientific Reports · doi:10.1038/s41598-020-68110-2 · Cited by 28 · see citing works
- Authors
- Rossi, M. A., & Stuber, G. D.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Corresponding author
- Stuber, Garret D.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2018-01
- Volume
- 27
- Issue
- 1
- Pages
- 42-56
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC5762260
- OpenAlex
- W2765429334
- Cited by
- 415
- References
- 188
- Citations by year
- 2026: 38 · 2025: 57 · 2024: 68 · 2023: 54 · 2022: 56 · 2021: 44 · 2020: 39 · 2019: 37 · 2018: 22
- FWCI
- 3.21
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
- UNC Libraries
- Funders
- National Institute on Drug Abuse (DA038168, DA032750)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK112564)
- Brain and Behavior Research Foundation
- 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
- Social Sciences › Psychology › Clinical Psychology › Eating Disorders and Behaviors
- Keywords
- hedonic feeding, food intake regulation, energy homeostasis, reward systems, neural circuits, food reward
- MeSH terms
- Animals, Brain, Feeding Behavior, Homeostasis, Humans, Nerve Net, Neurons, Reward
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