Cited by 355Neurotransmitter Receptor Influence on BehaviorRegulation of Appetite and ObesityNeuroscience and Neuropharmacology Research

The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.

Feeding and hypothalamic stimulation increase dopamine turnover in the accumbens

Hernandez, Luis, Hoebel, Bartley G.·1988·Physiology & Behavior

DOI 10.1016/0031-9384(88)90324-1

Open this paper in CoChat — free account

Abstract

The hypothesis that the dopaminergic system plays a role in feeding behavior was tested in three experiments. First, microdialysis was performed in the nucleus accumbens (NAC) at 20 min intervals during free feeding in rats at 80% of normal body weight. Extracellular concentration of dopamine (DA), dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA) increased significantly during eating indicating an increase in DA turnover. Second, microdialysis samples were collected from the NAC during bar pressing with a) a signal light on and food available, b) the light on but no food available, c) neither light nor food. Only when food was available did extracellular DA, DOPAC and HVA increase significantly. This increase in DA turnover occurred in the accumbens but not in the ventral striatum. Third, electrical stimulation of the perifornical lateral hypothalamus (LH) that was capable of inducing feeding increased extracellular DA, DOPAC and HVA in the NAC. This occurred whether the animal had food to eat or not. The effect of LH stimulation on DA turnover resembled the effects of free feeding and operant feeding in Experiments 1 and 2. Perifornical LH stimulation did not increase dopamine turnover in the ventral striatum. The results show that perifornical LH stimulation activates the mesolimbic dopamine system and that dopamine release in the accumbens is involved in feeding. The increase in dopamine turnover outlasted the consummatory act. This suggests that accumbens dopamine may be related to sensory input, feeding reflexes, food reward or memory processes and not just to the consummatory act itself.

Integrity signals

Registry

Crossref · 10.1016/0031-9384(88)90324-1

Cites

36 of 36 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Stereotaxic mapping of the monoamine pathways in the rat brain
Ungerstedt, U. (1971) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.1971.tb10998.x · Cited by 3,819
The Study of Instinct
Rowan, W., & Tinbergen, N. (1952) · Bird-Banding · doi:10.2307/4510368 · Cited by 2,706
Progress in Psychobiology and Physiological Psychology
Fluharty, S. J., & Grill, H. J. (2003) · Progress in psychobiology and physiological psychology · doi:10.1108/s0363-0951200318 · Cited by 1,701
Adipsia and Aphagia after 6‐Hydroxydopamine Induced Degeneration of the Nigro‐striatal Dopamine System
Ungerstedt, U. (1971) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.1971.tb11001.x · Cited by 1,294
Hypothalamic control of food intake in rats and cats.
Anand, B. K., & Brobeck, J. R. (1951) · PubMed · Cited by 1,197
The organization of the ascending catecholamine neuron systems in the rat brain as revealed by the glyoxylic acid fluorescence method.
Lindvall, O., & Björklund, A. (1974) · PubMed · Cited by 1,131
Afferent connections of the habenular nuclei in the rat. A horseradish peroxidase study, with a note on the fiber‐of‐passage problem
Herkenham, M. A., & Nauta, W. J. H. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901730107 · Cited by 798
Sensory Neglect Produced by Lateral Hypothalamic Damage
Marshall, J. F., Turner, B. H., & Teitelbaum, P. (1971) · Science · doi:10.1126/science.174.4008.523 · Cited by 411
Efferents and afferents of the ventral tegmental-A10 region studied after local injection of [3H]leucine and horseradish peroxidase
Simon, H., Moal, M. L., & Calas, A. (1979) · Brain Research · doi:10.1016/0006-8993(79)90085-4 · Cited by 401
Hypothalamic Control of Feeding and Self-Stimulation
Hoebel, B. G., & Teitelbaum, P. (1962) · Science · doi:10.1126/science.135.3501.375 · Cited by 389
Self-citation

Show all 36 references

Research works printed but not linked: 3

Brugger, 1943, Fresstrieb als hypothalamisches symptom, Helv. Physiol. Pharmacol. Acta, 1, 183
Collier, 1983, Life in a closed economy: The ecology of learning and motivation, vol. 3
Morgane, 1979, Historical and modern concepts of hypothalamic organization and function, vol. 1, 1

Sorted by citations

Items 201–300 of 355

Effects of antibodies to dynorphin A and β-endorphin on lateral hypothalamic self-stimulation in ad libitum fed and food-deprived rats
Carr, K. D. (1990) · Brain Research · doi:10.1016/0006-8993(90)90106-l · Cited by 29
Food intake and lateral hypothalamic self-stimulation covary after medial hypothalamic lesions or ventral midbrain 6-hydroxydopamine injections that cause obesity.
Hernández, L., & Hoebel, B. G. (1989) · Behavioral Neuroscience · doi:10.1037//0735-7044.103.2.412 · Cited by 29
Self-citation
D2 receptors in the ventrolateral striatum are involved in feeding behavior in rats
Inoue, K. (1995) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(94)00275-n · Cited by 29
Scarce Means with Alternative Uses: Robbins’ Definition of Economics and Its Extension to the Behavioral and Neurobiological Study of Animal Decision Making
Shizgal, P. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00020 · Cited by 30
Nutritional Controls of Food Reward
Fernandes, M. F., Sharma, S., Hryhorczuk, C., Auguste, S., & Fulton, S. (2013) · Canadian Journal of Diabetes · doi:10.1016/j.jcjd.2013.04.004 · Cited by 27
Common Neural Mechanisms of Palatable Food Intake and Drug Abuse: Knowledge Obtained with Animal Models
Blanco-Gandía, M. C., Miñarro, J., & Rodríguez‐Arias, M. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200213123608 · Cited by 28
Electrophysiological evidence of mediolateral functional dichotomy in the rat accumbens during cocaine self‐administration: tonic firing patterns
Fabbricatore, A. T., Ghitza, U. E., Prokopenko, V. F., & West, M. O. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07033.x · Cited by 26
Laugh Away the Fat? Therapeutic Humor in the Control of Stress-induced Emotional Eating
Bast, E. S., & Berry, E. M. (2014) · Rambam Maimonides Medical Journal · doi:10.5041/rmmj.10141 · Cited by 25
The Power of Integrative Peptides to Reinforce Behavior by Releasing Dopaminea
Hoebel, B. G., Rada, P. V., Mark, G. P., & Hernández, L. (1994) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1994.tb19805.x · Cited by 26
Self-citation
Feeding-related dopamine in the amygdala of freely moving rats
Hajnal, A. S., & Lénárd, L. (1997) · Neuroreport · doi:10.1097/00001756-199708180-00033 · Cited by 26
Amphetamine-induced rapid-onset sensitization: Role of novelty, conditioning and behavioral parameters
ALVAREZ, J., Fukushiro, D. F., Tatsu, J. A. O., DECARVALHO, E., Gandolfi, A. J., Tsuchiya, J., Carrara‐Nascimento, P. F., Lima, M. M. S., Bellot, R. G., & Frussa‐Filho, R. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2006.03.010 · Cited by 26
Reward Linked to Increased Natural Killer Cell Activity in Rats
Wenner, M., Kawamura, N., Ishikawa, T., & Matsuda, Y. (1999) · NeuroImmunoModulation · doi:10.1159/000026414 · Cited by 26
Effect of auditory stimulation on parasympathetic nerve activity in urethane-anesthetized rats.
Nakamura, T., Tanida, M., Niijima, A., & Nagai, K. (2009) · PubMed · Cited by 25
Dopamine systems and biological rhythms: Let’s get a move on
Tang, Q., Assali, D. R., Güler, A. D., & Steele, A. D. (2022) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2022.957193 · Cited by 28
A search for the metabolic signal that sensitizes lateral hypothalamic self-stimulation in food-restricted rats
de Vaca, S. C., Holiman, S., & Carr, K. D. (1998) · Physiology & Behavior · doi:10.1016/s0031-9384(98)00050-x · Cited by 25
Sulpiride increases and dopamine decreases intracranial temperature in rats when injected in the lateral hypothalamus: an animal model for the neuroleptic malignant syndrome?
Parada, M. A., de Parada, M. P., Rada, P. V., & Hernandez, L. (1995) · Brain Research · doi:10.1016/0006-8993(94)01455-q · Cited by 25
Self-citation
Dopaminergic enhancement of local food‐seeking is under global homeostatic control
Beeler, J. A., Frazier, C. R. M., & Zhuang, X. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07916.x · Cited by 25
Individual differences in the feeding effects of amphetamine: role of nucleus accumbens dopamine and circadian factors
Sills, T. L., Baird, J. P., & Vaccarino, F. J. (1993) · Psychopharmacology · doi:10.1007/bf02244913 · Cited by 23
The controls of eating: brain meanings of food stimuli
Smith, G. P. (2000) · Progress in brain research · doi:10.1016/s0079-6123(08)62137-8 · Cited by 24
The appetite suppressant, d-fenfluramine, decreases self-stimulation at a feeding site in the lateral hypothalamus
McClelland, R. C., Sarfaty, T., Hernández, L., & Hoebel, B. G. (1989) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(89)90171-8 · Cited by 24
Self-citation
Endocannabinoid-Dependent Modulation of Phasic Dopamine Signaling Encodes External and Internal Reward-Predictive Cues
Wenzel, J. M., & Cheer, J. F. (2014) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2014.00118 · Cited by 23
Circadian entrainment by food and drugs of abuse
Gillman, A. G., Rebec, G. V., Pecoraro, N. C., & Kosobud, A. (2019) · Behavioural Processes · doi:10.1016/j.beproc.2019.05.017 · Cited by 24
Regulation of ingestion by CRF and bombesin-like peptides: distinct meal-related peptide level changes
Plamondon, H., & Merali, Z. (1997) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1997.272.1.r268 · Cited by 23
Food reward depends on TLR4 activation in dopaminergic neurons
Li, Y., Chen, L., Zhao, W., Sun, L., Zhang, R., Zhu, S., Xie, K., Feng, X., Wu, X., Sun, Z., et al. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105659 · Cited by 23
Impact of High Fat Diet and Ethanol Consumption on Neurocircuitry Regulating Emotional Processing and Metabolic Function
Coker, C. R., Keller, B. N., Arnold, A. C., & Silberman, Y. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.601111 · Cited by 25
Physiologic and Neural Controls of Eating
Moran, T. H., & Ladenheim, E. E. (2016) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2016.07.009 · Cited by 22
Nicotine as an Addictive Substance: A Critical Examination of the Basic Concepts and Empirical Evidence
Atrens, D. M. (2001) · Journal of Drug Issues · doi:10.1177/002204260103100202 · Cited by 22
DRD4 and SLC6A3 gene polymorphisms are associated with food intake and nutritional status in children in early stages of development
Fontana, C., Vítolo, M. R., Campagnolo, P. D. B., Mattevi, V. S., Genro, J. P., & Almeida, S. (2015) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2015.07.030 · Cited by 20
Neurobiology of aversive states
Umberg, E. N., & Pothos, E. N. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.04.045 · Cited by 22
Therapeutic Applications for Agents that Act at CB1 and CB2 Receptors
Pertwee, R. G., & Thomas, A. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-503-9_13 · Cited by 20
Food Addiction Spectrum: A Theoretical Model from Normality to Eating and Overeating Disorders
Piccinni, A., Marazziti, D., Vanelli, F., Franceschini, C., Baroni, S., Costanzo, D., Cremone, I. M., Veltri, A., & Dell’Osso, L. (2015) · Current Medicinal Chemistry · doi:10.2174/0929867322666150227153015 · Cited by 22
Mesolimbic dopaminergic mechanisms underlying individual differences in sugar consumption and amphetamine hyperlocomotion in Wistar rats
Sills, T. L., Onalaja, A. O., & Crawley, J. N. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00201.x · Cited by 19
Dopamine D1 and opioid receptor antagonist-induced reductions of fructose and saccharin intake in BALB/c and SWR inbred mice
Kraft, T. T., Huang, D., Natanova, E., Lolier, M., Yakubov, Y., Magna, S. L., Warshaw, D., Sclafani, A. J., & Bodnar, R. J. (2015) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2015.01.010 · Cited by 18
Afferent neuropeptide Y projections to the ventral tegmental area in normal‐weight male Wistar rats
Gumbs, M. C. R., Vuuregge, A. H., Eggels, L., Unmehopa, U. A., Lamuadni, K., Mul, J. D., & la Fleur, S. E. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24698 · Cited by 18
Dopamine–Acetylcholine Interaction in the Rat Lateral Hypothalamus in the Control of Locomotion
de Parada, M. P., Parada, M. A., Rada, P. V., Hernandez, L., & Hoebel, B. G. (2000) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(99)00244-0 · Cited by 18
Self-citation
Role of 5-hydroxytryptamine 1B (5-HT1B) receptors in the regulation of ethanol intake in rodents
Sari, Y. (2012) · Journal of Psychopharmacology · doi:10.1177/0269881112463126 · Cited by 18
Effects of Intermittent Fasting on Hypothalamus–Pituitary–Thyroid Axis, Palatable Food Intake, and Body Weight in Stressed Rats
García-Luna, C., Prieto, I., Soberanes-Chávez, P., Alvarez‐Salas, E., Torre-Villalvazo, I., Matamoros‐Trejo, G., & de Gortari, P. (2023) · Nutrients · doi:10.3390/nu15051164 · Cited by 17
Effect of Orexin A antagonist (SB-334867) infusion into the nucleus accumbens on consummatory behavior and alcohol preference in Wistar rats
Ganaraja, B., Mayannavar, S., Rashmi, K. M., Rao, Y. D., & Yadav, S. J. (2016) · Indian Journal of Pharmacology · doi:10.4103/0253-7613.174528 · Cited by 17
Monitoring In Vivo Neural Activity to Understand Gut–Brain Signaling
Alhadeff, A. L. (2021) · Endocrinology · doi:10.1210/endocr/bqab029 · Cited by 18
Development of ?3-adrenoceptor agonists as antiobesity and antidiabetes drugs in humans: Current status and future prospects
Weyer, C., & de Souza, C. J. (2000) · Drug Development Research · doi:10.1002/1098-2299(200010)51:2 · Cited by 16
Exogenously administered leptin leads to weight loss and increased physical activity in the marsupial Sminthopsis crassicaudata
Wittert, G., Turnbull, H., & Hope, P. J. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.06.012 · Cited by 15
Blocking alpha2A adrenoceptors, but not dopamine receptors, augments bupropion‐induced hypophagia in rats
Janhunen, S. K., la Fleur, S. E., & Adan, R. A. H. (2013) · Obesity · doi:10.1002/oby.20581 · Cited by 14
The interactions between adipose tissue secretions and Parkinson's disease: The role of leptin
Ekraminasab, S., Dolatshahi, M., Sabahi, M., Mardani, M., & Rashedi, S. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15594 · Cited by 11
Pavlovian conditioning and cross-sensitization studies raise challenges to the hypothesis that overeating is an addictive behavior
Harb, M. R., & Almeida, O. F. X. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.28 · Cited by 13
Preclinical Models of Stress and Environmental Influences on Binge Eating
Bonaventura, M. V. M. D., Bonaventura, E. M. D., Polidori, C., & Cifani, C. (2020) · Springer eBooks · doi:10.1007/978-3-030-43562-2_7 · Cited by 13
Utility of ‘substance use disorder’ as a heuristic for understanding overeating and obesity
O’Connor, R. M., & Kenny, P. J. (2022) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2022.110580 · Cited by 14
Behavioral significance of phasic changes in mesolimbic dopamine-dependent electrochemical signal associated with heroin self-injections
Kiyatkin, E. A. (1994) · Journal of Neural Transmission · doi:10.1007/bf01294787 · Cited by 13
Appetitive Needs and Addiction
Sussman, S. Y., & Pakdaman, S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.004 · Cited by 12
Individual differences in the feeding response to CCKB antagonists: Role of the nucleus accumbens
Sills, T. L., & Vaccarino, F. J. (1996) · Peptides · doi:10.1016/0196-9781(96)00032-0 · Cited by 12
Chronic food restriction alters purinergic receptor mRNA expression in the nucleus accumbens of the rat
Krügel, U., Seidel, B., Spies, O., Kittner, H., Illés, P., & Kieß, W. (2003) · Drug Development Research · doi:10.1002/ddr.10207 · Cited by 12
Accumbens Dopamine is a Physiological Correlate of the Rewarding and Motivating Effects of Food
Smith, G. P. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-48643-1_2 · Cited by 12
Food and Fluid Intake
Moran, T. H., & Sakai, R. R. (2003) · Wiley eBooks · doi:10.1002/0471264385.wei0311 · Cited by 12
Increased Feeding and Food Hoarding following Food Deprivation Are Associated with Activation of Dopamine and Orexin Neurons in Male Brandt's Voles
Zhang, X., Yang, H.-D., Zhang, Q., Wang, Z., & Wang, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026408 · Cited by 11
Feeding behavior as seen through the prism of brain microdialysis
Hernández, L., Paredes, D., & Rada, P. V. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.04.031 · Cited by 10
Prosocial effects of prolactin in male rats: Social recognition, social approach and social learning
Donhoffner, M. E., Saleh, S. A., Schink, O., & Wood, R. I. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.09.011 · Cited by 10
Refeeding after 72 hour fasting alters neuropeptide Y and monoamines in various cerebral areas in the rat
Pagès, N., Orosco, M., Rough, C., Yao, O., Jacquot, C., & Bohuon, C. (1993) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(93)90406-t · Cited by 10
Anticipation: An Essential Feature of Anhedonia
Phillips, A. G., & Ahn, S. (2022) · Current topics in behavioral neurosciences · doi:10.1007/7854_2022_317 · Cited by 9
Effects of intracisternal vs. intrahypothalamic 5,7-DHT on feeding elicited by hypothalamic infusion of NE
Coscina, D. V., & Rooy, E. C. H. D. (1992) · Brain Research · doi:10.1016/0006-8993(92)91488-z · Cited by 9
Midbrain and Lateral Nucleus Accumbens Dopamine Depletion Affects Free-choice High-fat high-sugar Diet Preference in Male Rats
Joshi, A., Faivre, F., la Fleur, S. E., & Barrot, M. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.05.022 · Cited by 10
Dissociation of prefrontal cortex and nucleus accumbens dopaminergic systems in conditional learning in rats
George, D. N., Jenkins, T. A., & Killcross, S. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.06.028 · Cited by 8
Anterior Insular-nucleus Accumbens Pathway Controls Refeeding-induced Analgesia under Chronic Inflammatory Pain Condition
Lee, G. J., Kim, Y. J., Shim, S. W., Lee, K., & Oh, S. B. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.05.025 · Cited by 8
Electrical brain stimulation reward: a model of drug reward and euphoria
Lewis, M. J. (1993) · Techniques in the behavioral and neural sciences · doi:10.1016/b978-0-444-81444-9.50020-1 · Cited by 8
Dopaminergic and GABAergic Regulation of Alcohol‐Motivated Behaviors: Novel Neuroanatomical Substrates
June, H. L., & Eiler, W. J. A. (2007) · doi:10.1002/9780470101001.hcn036 · Cited by 8
Qualitative Approaches to the Study of Substance and Behavioral Addictions
Simpson, K. A., & Bluthenthal, R. N. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.013 · Cited by 10
Lateral Hypothalamic Control of Energy Balance
Kurt, G., Woodworth, H. L., & Leinninger, G. M. (2017) · Colloquium Series on Integrated Systems Physiology From Molecule to Function · doi:10.4199/c00159ed1v01y201711isp079 · Cited by 7
Genetic variation of the dopamine D2 receptor gene: association with the reinforcing value of food and eating in the absence of hunger in Chilean children
Obregón, A. M., Vega, M. V., Goldfield, G. S., & Llewellyn, C. H. (2020) · Nutrición Hospitalaria · doi:10.20960/nh.02897 · Cited by 7
Nutrition, Feeding and Drinking Behaviour, and Welfare
Savory, J. (2009) · Animal welfare · doi:10.1007/978-90-481-3650-6_7 · Cited by 7
Dopamine Release by Sucrose
Hajnal, A. S., & Norgren, R. (2008) · Elsevier eBooks · doi:10.1016/b978-012370880-9.00099-2 · Cited by 6
Impact of a History of Caloric Restriction and a Frustration Stress Manipulation on Binge-Like Eating Behavior in Female Rats: Preclinical Results
Bonaventura, M. V. M. D., Bonaventura, E. M. D., Botticelli, L., & Cifani, C. (2020) · Neuromethods · doi:10.1007/978-1-0716-0924-8_13 · Cited by 6
7-OH-DPAT selectively reduces intake of both chow and high fat diets in different food intake regimens
McQuade, J.-A., Benoit, S. C., Woods, S. C., & Seeley, R. J. (2003) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2003.09.008 · Cited by 6
Effect of adrenalectomy on cocaine facilitation of medial prefrontal cortex self-stimulation
Carr, K. D., & Abrahamsen, G. C. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01487-x · Cited by 6
Effect of stable iodine on uptake of radioiodine in sheep.
BUSTAD, L. K., WARNER, D. E., & Kornberg, H. A. (1958) · PubMed · Cited by 6
Serotonin and Dopamine Mimic Glucose-Induced Reinforcement in C. elegans: Potential Role of NSM Neurons and the Serotonin Subtype 4 Receptor
Schwartz, E. K. C., Sosner, E., Desmond, H. E., Lum, S. J., Sze, J. Y., & Mobbs, C. V. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.783359 · Cited by 5
Intracranial self-stimulation of the dorsal raphe sensitizes psychostimulant locomotion.
Boye, S. M., Grant, R. J., & Tawfik, V. L. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.3.550 · Cited by 5
Substance and Behavioral Addictions Assessment Instruments
Grigsby, T. J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.012 · Cited by 6
Developmental or adult-onset deletion of neurotensin receptor-1 from dopamine neurons differentially reduces body weight
Perez‐Bonilla, P., Ramirez‐Virella, J., Menon, P., Troyano‐Rodriguez, E., Arriaga, S. K., Makela, A. G., Bugescu, R., Beckstead, M. J., & Leinninger, G. M. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.874316 · Cited by 5
DA1 Receptor Activity Opposes Anorectic Responses to Amino Acid-Imbalanced Diets
Aja, S. M. (1999) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(98)00213-5 · Cited by 5
Neonatal cardiac vagal tone and school-age developmental outcome in very low birth weight infants
Doussard-Roosevelt, J. A., McClenny, B. D., & Porges, S. W. (2000) · Developmental Psychobiology · doi:10.1002/1098-2302(2001)38:1 · Cited by 87
Diazepam-Induced Hyperphagia in Mice is Sensitive to Quinpirole.
Rahminiwati, M., & Nishimura, M. (1999) · Journal of Veterinary Medical Science · doi:10.1292/jvms.61.777 · Cited by 5
Drinking sucrose enhances quinpirole-induced yawning in rats
Baladi, M. G., Newman, A. H., Thomas, Y. M., & France, C. P. (2011) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e32834d0f3c · Cited by 4
Translating Animal Models of Obesity and Diabetes to the Clinic
Geiger, B. M., & Pothos, E. N. (2019) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-803161-2.00001-1 · Cited by 4
Prevention and Treatment of Sex Addiction
Reid, R. C., Grubbs, J. B., & Kraus, S. W. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.025 · Cited by 4
Biopsychological investigation of hedonic processes in individuals susceptible to overeating : role of liking and wanting in trait binge eating
Dalton, M. (2013) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York) · Cited by 4
Gaming Disorder and Its Treatment
Griffiths, M. D., Kuss, D. J., & Pontes, H. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.029 · Cited by 6
Suchtaspekte bei Adipositas
Kiefer, F., & Grosshans, M. (2014) · Springer eBooks · doi:10.1007/978-3-642-38364-9_6 · Cited by 3
Exploring Habits in Anorexia Nervosa: Promise, Pitfalls, and Progress
Foerde, K. (2025) · Current Psychiatry Reports · doi:10.1007/s11920-025-01588-7 · Cited by 19
Treatment of Alcohol, Tobacco, and Other Drug (ATOD) Misuse
Sussman, S. Y., & Bolshakova, M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.022 · Cited by 3
The Role of Culture in Addiction
Hoffman, B. R., & Unger, J. B. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.018 · Cited by 3
Chapter 4.2 Microdialysis of dopamine and norepinephrine during conditioning and operant behaviour
Feenstra, M. G. P. (2006) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(06)16018-x · Cited by 3
Preweaning iron deficiency increases non-contingent responding during cocaine self-administration in rats
Jenney, C. B., Alexander, D. N., Jones, B. C., Unger, E. L., & Grigson, P. S. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.09.007 · Cited by 3
The effects of the dopamine D2/3 agonist quinpirole on incentive value and palatability-based choice in a rodent model of attention-deficit/hyperactivity disorder
Natsheh, J. Y., Espinoza, D., Bhimani, S., & Shiflett, M. W. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05931-7 · Cited by 5
Trained and Amphetamine‐Induced Circling Behavior in Lesioned,Transplanted Rats
Richards, J. B., Sabol, K. E., Kriek, E. H., & Freed, C. R. (1993) · Neural Plasticity · doi:10.1155/np.1993.157 · Cited by 3
Psychoanalytical Considerations of Emotion Regulation Disorders in Multiple Complex-Traumatized Children—A Study Protocol of the Prospective Study MuKi
Hug, F., Degen, T., Meurs, P., & Fischmann, T. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.809616 · Cited by 2
Passionate Love Addiction: An Evolutionary Survival Mechanism That Can Go Terribly Wrong
Bolshakova, M., Fisher, H. E., Aubin, H., & Sussman, S. Y. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.026 · Cited by 2
Philosophical Issues in the Addictions
Glackin, S. N. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.007 · Cited by 2
Prevention and Treatment
(2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.020 · Cited by 2
Extracellular glutamate decrease in accumbens following cued food delivery
Chapman, M. A., Roll, J. M., Park, S., & Galloway, M. P. (2003) · Neuroreport · doi:10.1097/00001756-200305230-00017 · Cited by 2
Dopamine mechanisms in learning and memory: evidence from rodent studies
Cruz, J. A. D. A. D. (2014) · doi:10.26481/dis.20140320jd · Cited by 2
Food Hedonics
Skibicka, K. P., & Kanoski, S. E. (2016) · doi:10.1002/9781118839317.ch5 · Cited by 2
CCK, Addiction and Anxiety
Vaccarino, F. J. (1995) · Neuroscience intelligence unit · doi:10.1007/978-3-662-21705-4_7 · Cited by 2

Authors: Hernandez, L., & Hoebel, B. G.
Affiliations: Princeton University (US)
Venue: Physiology & Behavior
Publisher: Elsevier BV
Published: 1988-01
Volume: 44
Issue: 4-5
Pages: 599-606
ISSN: 0031-9384 (ISSN-L)
DOI: 10.1016/0031-9384(88)90324-1
OpenAlex: W2066841804
Cited by: 355
References: 36
Citations by year: 2026: 1 · 2025: 3 · 2023: 3 · 2022: 12 · 2021: 7 · 2020: 49 · 2019: 9 · 2018: 7 · 2017: 6 · 2016: 5 · 2015: 11 · 2014: 11 · 2013: 9 · 2012: 14
FWCI: 2.07
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Physiology & Behavior (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute on Drug Abuse (DA 03597)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: feeding behavior, dopamine turnover, nucleus accumbens, mesolimbic dopamine system, extracellular dopamine, dihydroxyphenylacetic acid, homovanillic acid, ventral striatum, food reward
MeSH terms: Animals, Body Weight, Corpus Striatum, Dopamine, Eating, Electric Stimulation, Female, Hunger, Hypothalamic Area, Lateral, Male, Neural Pathways, Nucleus Accumbens, Rats, Inbred Strains, Receptors, Dopamine, Septal Nuclei, Rats

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

Feeding and hypothalamic stimulation increase dopamine turnover in the accumbens

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks