Differential expression of motivational stimulus properties by dopamine in nucleus accumbens shell versus core and prefrontal cortex

The rat brain in stereotaxic coordinates

Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959 · see citing works

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

A neural substrate of prediction and reward

Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388 · see citing works

A theory of Pavlovian conditioning : Variations in the effectiveness of reinforcement and nonreinforcement

Rescorla, R. A. (1972) · Medical Entomology and Zoology · Cited by 7,268 · see citing works

Predictive reward signal of dopamine neurons

Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.1 · Cited by 4,564 · see citing works

What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience?

Berridge, K. C., & Robinson, T. E. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00019-8 · Cited by 4,127 · see citing works

Responses of monkey dopamine neurons to reward and conditioned stimuli during successive steps of learning a delayed response task

Schultz, W., Apicella, P., & Ljungberg, T. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-03-00900.1993 · Cited by 1,291 · see citing works

The taste reactivity test. I. Mimetic responses to gustatory stimuli in neurologically normal rats

Grill, H. J., & Norgren, R. (1978) · Brain Research · doi:10.1016/0006-8993(78)90568-1 · Cited by 1,203 · see citing works

Differential effect of stress on in vivo dopamine release in striatum, nucleus accumbens, and medial frontal cortex

Abercrombie, E. D., Keefe, K. A., DiFrischia, D. S., & Zigmond, M. J. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb09224.x · Cited by 1,106 · see citing works

Cannabinoid and Heroin Activation of Mesolimbic Dopamine Transmission by a Common µ 1 Opioid Receptor Mechanism

Tanda, G., Pontieri, F. E., & Chiara, G. D. (1997) · Science · doi:10.1126/science.276.5321.2048 · Cited by 1,079 · see citing works

Effects of nicotine on the nucleus accumbens and similarity to those of addictive drugs.

Pontieri, F. E., Tanda, G., Orzi, F., & Chiara, G. D. (1996) · Nature · doi:10.1038/382255a0 · Cited by 1,073 · see citing works

Neuroleptics and operant behavior: The anhedonia hypothesis

Wise, R. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00010372 · Cited by 1,022 · see citing works

Mesolimbocortical and nigrostriatal dopamine responses to salient non-reward events

Horvitz, J. C. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00019-1 · Cited by 967 · see citing works

Sensory specific satiety in man☆

Rolls, B. J., Rolls, E. T., Rowe, E. A., & Sweeney, K. F. (1981) · Physiology & Behavior · doi:10.1016/0031-9384(81)90310-3 · Cited by 884 · see citing works

Intravenous cocaine, morphine, and amphetamine preferentially increase extracellular dopamine in the "shell" as compared with the "core" of the rat nucleus accumbens.

Pontieri, F. E., Tanda, G., & Chiara, G. D. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.26.12304 · Cited by 868 · see citing works

Preferential activation of midbrain dopamine neurons by appetitive rather than aversive stimuli

Mirenowicz, J., & Schultz, W. (1996) · Nature · doi:10.1038/379449a0 · Cited by 829 · see citing works

Measuring hedonic impact in animals and infants: microstructure of affective taste reactivity patterns

Berridge, K. (2000) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(99)00072-x · Cited by 721 · see citing works

Amphetamine-induced dopamine release in human ventral striatum correlates with euphoria

Drevets, W. C., Gautier, C., Price, J. C., Kupfer, D. J., Kinahan, P. E., Grace, A. A., Price, J. L., & Mathis, C. A. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(00)01038-6 · Cited by 706 · cited 2× · see citing works

Neuroleptic-Induced "Anhedonia" in Rats: Pimozide Blocks Reward Quality of Food

Wise, R. A., Spindler, J., de Wit, H., & Gerberg, G. J. (1978) · Science · doi:10.1126/science.566469 · Cited by 636 · see citing works

The role of dopamine in drug abuse viewed from the perspective of its role in motivation

Chiara, G. D. (1995) · Drug and Alcohol Dependence · doi:10.1016/0376-8716(95)01118-i · Cited by 624 · see citing works

The involvement of nucleus accumbens dopamine in appetitive and aversive motivation

Salamone, J. D. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90153-8 · Cited by 584 · see citing works

Is the short-latency dopamine response too short to signal reward error?

Redgrave, P., Prescott, T. J., & Gurney, K. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01373-3 · Cited by 506 · see citing works

Sensory-specific Satiety

Rolls, B. J. (2009) · Nutrition Reviews · doi:10.1111/j.1753-4887.1986.tb07593.x · Cited by 481 · see citing works

Pharmacological characterization of dopamine systems in the nucleus accumbens core and shell

Deutch, A. Y., & Cameron, D. S. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90007-o · Cited by 461 · see citing works

Differential responsiveness of dopamine transmission to food-stimuli in nucleus accumbens shell/core compartments.

Bassareo, V., & Chiara, G. D. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00583-1 · Cited by 433 · see citing works

Selective activation of dopamine transmission in the shell of the nucleus accumbens by stress

Kalivas, P. W., & Duffy, P. (1995) · Brain Research · doi:10.1016/0006-8993(95)00013-g · Cited by 395 · see citing works

Differential Influence of Associative and Nonassociative Learning Mechanisms on the Responsiveness of Prefrontal and Accumbal Dopamine Transmission to Food Stimuli in Rats FedAd Libitum

Bassareo, V., & Chiara, G. D. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-02-00851.1997 · Cited by 375 · see citing works

Involvement of the central nucleus of the amygdala and nucleus accumbens core in mediating Pavlovian influences on instrumental behaviour

Hall, J., Parkinson, J. A., Connor, T. M., Dickinson, A., & Everitt, B. J. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01577.x · Cited by 355 · see citing works

Dopaminergic correlates of motivated behavior: importance of drive

Wilson, C., Nomikos, G., Collu, M., & Fibiger, H. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-07-05169.1995 · Cited by 294 · see citing works

Response-reinforcement learning is dependent on N -methyl- d -aspartate receptor activation in the nucleus accumbens core

Kelley, A. E., Smith‐Roe, S. L., & Holahan, M. R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.22.12174 · Cited by 293 · see citing works

Brain microdialysis and its application for the study of animal behaviour

Westerink, B. H. C. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(95)80001-8 · Cited by 284 · see citing works

Olfactory Sensory-Specific Satiety in Humans

Rolls, E. T., & ROLLS, J. (1997) · Physiology & Behavior · doi:10.1016/s0031-9384(96)00464-7 · Cited by 284 · see citing works

Burst activity of ventral tegmental dopamine neurons is elicited by sensory stimuli in the awake cat

Horvitz, J. C., Stewart, T., & Jacobs, B. L. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00265-5 · Cited by 283 · see citing works

Modulation of feeding‐induced activation of mesolimbic dopamine transmission by appetitive stimuli and its relation to motivational state

Bassareo, V., & Chiara, G. D. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00843.x · Cited by 278 · see citing works

Reciprocal changes in prefrontal and limbic dopamine responsiveness to aversive and rewarding stimuli after chronic mild stress: implications for the psychobiology of depression.

Chiara, G. D., Loddo, P., & Tanda, G. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00236-x · Cited by 266 · see citing works

Stress-induced enhancement of dopamine and acetylcholine release in limbic structures: role of corticosterone

Imperato, A., Puglisi-Allegra, S., Casolini, P., Zocchi, A., & Angelucci, L. (1989) · European Journal of Pharmacology · doi:10.1016/0014-2999(89)90735-8 · Cited by 203 · see citing works

A conditioned stimulus decreases extracellular dopamine in the nucleus accumbens after the development of a learned taste aversion

Mark, G. P., Blander, D. S., & Hoebel, B. G. (1991) · Brain Research · doi:10.1016/0006-8993(91)90946-s · Cited by 181 · see citing works

The behavioral neurochemistry of motivation: methodological and conceptual issues in studies of the dynamic activity of nucleus accumbens dopamine

Salamone, J. D. (1996) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(95)00125-5 · Cited by 156 · see citing works

A Role for Dopamine D1 Receptors of the Nucleus Accumbens Shell in Conditioned Taste Aversion Learning

Fenu, S., Bassareo, V., & Chiara, G. D. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-17-06897.2001 · Cited by 128 · see citing works

On the preferential release of dopamine in the nucleus accumbens by amphetamine: further evidence obtained by vertically implanted concentric dialysis probes

Chiara, G. D., Tanda, G., Frau, R., & Carboni, E. (1993) · Psychopharmacology · doi:10.1007/bf02244939 · Cited by 125 · see citing works

Estimation of in-vivo neurotransmitter release by brain microdialysis

Chiara, G. D., Tanda, G., & Carboni, E. (1996) · Behavioural Pharmacology · doi:10.1097/00008877-199611000-00009 · Cited by 116 · see citing works

Mianserin markedly and selectively increases extracellular dopamine in the prefrontal cortex as compared to the nucleus accumbens of the rat

Tanda, G., Bassareo, V., & Chiara, D. (1996) · Psychopharmacology · doi:10.1007/bf02246169 · Cited by 106 · see citing works

Non-psychostimulant drugs of abuse and anxiogenic drugs activate with differential selectivity dopamine transmission in the nucleus accumbens and in the medial prefrontal cortex of the rat

Bassareo, V., Tanda, G., Petromilli, P., Giua, C., & Chiara, G. D. (1996) · Psychopharmacology · doi:10.1007/bf02247433 · Cited by 93 · see citing works

Effects of Nicotine

Burn, J. H. (1968) · BMJ · doi:10.1136/bmj.1.5587.310-b · Cited by 50 · see citing works

Amphetamine-Induced Dopamine Release

Carson, R., Channing, M., Vuong, B., Watabe, H., Herscovitch, P., & Eckelman, W. (2001) · Elsevier eBooks · doi:10.1016/b978-012285751-5/50034-x · Cited by 33 · see citing works

Non-psychostimulant drugs of abuse and anxiogenic drugs activate with differential selectivity dopamine transmission in the nucleus accumbens and in the medial prefrontal cortex of the rat

Bassareo, V., Tanda, G., Petromilli, P., Giua, C., & Chiara, G. D. (1996) · Psychopharmacology · doi:10.1007/bf02246138 · Cited by 2 · see citing works

Dopamine in motivational control: rewarding, aversive, and alerting

Bromberg-Martin, E. S., Matsumoto, M., & Hikosaka, O. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.022 · Cited by 2,396 · 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

Dopamine in drug abuse and addiction: results from imaging studies and treatment implications

Volkow, N. D., Fowler, J. S., Wang, G.-J., & Swanson, J. M. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001507 · Cited by 1,101 · see citing works

Nucleus accumbens shell and core dopamine: differential role in behavior and addiction

Di Chiara, G. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00286-3 · Cited by 996 · see citing works

Unique properties of mesoprefrontal neurons within a dual mesocorticolimbic dopamine system

Lammel, S., Hetzel, A., Häckel, O., Jones, I., Liss, B., & Roeper, J. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.022 · Cited by 976 · see citing works

Dopamine and drug addiction: the nucleus accumbens shell connection

Di Chiara, G., Bassareo, V., Fenu, S., De Luca, M. A., Spina, L., Cadoni, C., Acquas, E., Carboni, E., Valentini, V., & Lecca, D. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.06.032 · Cited by 935 · see citing works

A Comprehensive Overview on Stress Neurobiology: Basic Concepts and Clinical Implications

Godoy, L. D., Rossignoli, M. T., Delfino-Pereira, P., Garcia‐Cairasco, N., & Umeoka, E. H. D. L. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00127 · Cited by 884 · see citing works

Reward and aversion in a heterogeneous midbrain dopamine system

Lammel, S., Lim, B. K., & Malenka, R. C. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.03.019 · Cited by 804 · see citing works

Projection-specific modulation of dopamine neuron synapses by aversive and rewarding stimuli

Lammel, S., Ion, D. I., Roeper, J., & Malenka, R. C. (2011) · Neuron · doi:10.1016/j.neuron.2011.03.025 · Cited by 766 · see citing works

Shape shifting pain: chronification of back pain shifts brain representation from nociceptive to emotional circuits

Hashmi, J. A., Baliki, M. N., Huang, L., Baria, A. T., Torbey, S., Hermann, K. M., Schnitzer, T. J., & Apkarian, A. V. (2013) · Brain · doi:10.1093/brain/awt211 · Cited by 762 · see citing works

Corticostriatal-hypothalamic circuitry and food motivation: Integration of energy, action and reward

Kelley, A. E., Baldo, B. A., Pratt, W. E., & Will, M. J. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.08.066 · Cited by 752 · see citing works

Drug addiction: the neurobiology of disrupted self-control

Baler, R. D., & Volkow, N. D. (2006) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2006.10.005 · Cited by 640 · see citing works

Predicting Value of Pain and Analgesia: Nucleus Accumbens Response to Noxious Stimuli Changes in the Presence of Chronic Pain

Baliki, M. N., Geha, P., Fields, H. L., & Apkarian, A. V. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.002 · Cited by 549 · see citing works

Reward system and addiction: what dopamine does and doesn’t do

DiChiara, G., & Bassareo, V. (2006) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2006.11.003 · Cited by 534 · see citing works

A Neural Circuit Mechanism for Encoding Aversive Stimuli in the Mesolimbic Dopamine System

de Jong, J. W., Afjei, S. A., Dorocic, I. P., Peck, J. R., Liu, C. J., Kim, C. K., Tian, L., Deisseroth, K. A., & Lammel, S. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.005 · Cited by 506 · see citing works

A neoHebbian framework for episodic memory; role of dopamine-dependent late LTP

Lisman, J., Grace, A. A., & Duzel, E. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.07.006 · Cited by 465 · see citing works

Beyond the reward hypothesis: alternative functions of nucleus accumbens dopamine

Salamone, J. D., Correa, M., Mingote, S., & Weber, S. (2004) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2004.09.004 · Cited by 454 · 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

The ventral basal ganglia, a selection mechanism at the crossroads of space, strategy, and reward.

Humphries, M. D., & Prescott, T. J. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.11.003 · Cited by 414 · see citing works

Nucleus Accumbens Subnuclei Regulate Motivated Behavior via Direct Inhibition and Disinhibition of VTA Dopamine Subpopulations

Yang, H., de Jong, J. W., Tak, Y., Peck, J., Bateup, H. S., & Lammel, S. (2018) · Neuron · doi:10.1016/j.neuron.2017.12.022 · Cited by 407 · see citing works

Exposure to appetitive food stimuli markedly activates the human brain

Wang, G.-J., Volkow, N. D., Telang, F., Jayne, M., Ma, J., Rao, M., Zhu, W., Wong, C. T., Pappas, N. R., Geliebter, A., et al. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.026 · Cited by 402 · see citing works

Sensitivity to reward: implications for overeating and overweight

Davis, C. A., Strachan, S. M., & Berkson, M. (2003) · Appetite · doi:10.1016/j.appet.2003.07.004 · Cited by 378 · see citing works

Sex differences in the neural mechanisms mediating addiction: a new synthesis and hypothesis

Becker, J. B., Perry, A. N., & Westenbroek, C. (2012) · Biology of Sex Differences · doi:10.1186/2042-6410-3-14 · Cited by 315 · see citing works

Discrete neurochemical coding of distinguishable motivational processes: insights from nucleus accumbens control of feeding

Baldo, B. A., & Kelley, A. E. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0741-z · Cited by 312 · see citing works

Cortical activation of accumbens hyperpolarization-active NMDARs mediates aversion-resistant alcohol intake

Seif, T., Chang, S., Simms, J. A., Gibb, S. L., Dadgar, J., Chen, B. T., Harvey, B. K., Dorit Ron, A., Messing, R. O., Bonci, A., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3445 · Cited by 310 · see citing works

Stress increases dynorphin immunoreactivity in limbic brain regions and dynorphin antagonism produces antidepressant‐like effects

Shirayama, Y., Ishida, H., Iwata, M., Hazama, G., Kawahara, R., & Duman, R. S. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02589.x · Cited by 305 · see citing works

The neuroscience of positive emotions and affect: Implications for cultivating happiness and wellbeing

Alexander, R., Aragón, O. R., Bookwala, J., Cherbuin, N., Gatt, J. M., Kahrilas, I. J., Kästner, N., Lawrence, A. B., Lowe, L. J., Morrison, R., et al. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.12.002 · Cited by 329 · see citing works

The role of mesolimbic dopamine in the development and maintenance of ethanol reinforcement

Gonzales, R. A., Job, M. O., & Doyon, W. M. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.06.002 · Cited by 297 · see citing works

Evidence of gender differences in the ability to inhibit brain activation elicited by food stimulation

Wang, G.-J., Volkow, N. D., Telang, F., Jayne, M., Ma, Y., Pradhan, K., Zhu, W., Wong, C. T., Thanos, P. K., Geliebter, A., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807423106 · Cited by 242 · see citing works

Dopamine Transmission in the Human Striatum during Monetary Reward Tasks

Zald, D. H., Boileau, I., El-Dearedy, W., Gunn, R., McGlone, F., Dichter, G. S., & Dagher, A. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.4643-03.2004 · Cited by 238 · see citing works

Phenotypic characterization of spatial cognition and social behavior in mice with ‘knockout’ of the schizophrenia risk gene neuregulin 1

O’Tuathaigh, C. M. P., Babovic, D., O’Sullivan, G. J., Clifford, J. J., Tighe, O., Croke, D. T., Harvey, R. P., & Waddington, J. L. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.03.051 · Cited by 230 · see citing works

Neurochemistry of the nucleus accumbens and its relevance to depression and antidepressant action in rodents

Shirayama, Y., & Chaki, S. (2006) · Current Neuropharmacology · doi:10.2174/157015906778520773 · Cited by 225 · see citing works

High intake of palatable food predicts binge-eating independent of susceptibility to obesity: an animal model of lean vs obese binge-eating and obesity with and without binge-eating

Boggiano, M. M., Artiga, A. I., Pritchett, C. E., Chandler-Laney, P. C., Smith, M., & Eldridge, A. J. (2007) · International Journal of Obesity · doi:10.1038/sj.ijo.0803614 · Cited by 207 · see citing works

Mesolimbic Dopamine and the Regulation of Motivated Behavior

Salamone, J. D., Pardo, M., Yohn, S. E., López-Cruz, L., SanMiguel, N., & Correa, M. (2015) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2015_383 · Cited by 204 · see citing works

The scientific study of inspiration in the creative process: challenges and opportunities

Oleynick, V. C., Thrash, T. M., LeFew, M. C., Moldovan, E. G., & Kieffaber, P. D. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00436 · Cited by 201 · see citing works

Dopamine: the salient issue

Ungless, M. A. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.10.001 · Cited by 190 · see citing works

Neurobehavioral foundation of environmental reactivity.

Moore, S. R., & Depue, R. A. (2015) · Psychological Bulletin · doi:10.1037/bul0000028 · Cited by 181 · see citing works

Dopamine D1 and D2 receptors in the nucleus accumbens core and shell mediate Pavlovian-instrumental transfer.Preprint

Lex, A., & Hauber, W. (2008) · Learning & memory (Cold Spring Harbor, N.Y.) · doi:10.1101/lm.978708 · Cited by 190 · see citing works

Dopamine and binge eating behaviors

Bello, N. T., & Hajnal, A. S. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.04.016 · Cited by 177 · see citing works

Learning to forget: manipulating extinction and reconsolidation processes to treat addiction

Torregrossa, M. M., & Taylor, J. R. (2013) · Psychopharmacology · doi:10.1007/s00213-012-2750-9 · Cited by 172 · see citing works

Context, emotion, and the strategic pursuit of goals: interactions among multiple brain systems controlling motivated behavior

Gruber, A. J., & McDonald, R. J. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00050 · Cited by 173 · see citing works

New insights into the specificity and plasticity of reward and aversion encoding in the mesolimbic system

Volman, S. F., Lammel, S., Margolis, E. B., Kim, Y., Richard, J. M., Roitman, M. F., & Lobo, M. K. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3250-13.2013 · Cited by 168 · see citing works

Regulation of anxiety and initiation of sexual behavior by CREB in the nucleus accumbens

Barrot, M., Wallace, D. L., Bolaños, C. A., Graham, D. L., Perrotti, L. I., Neve, R. L., Chambliss, H., Yin, J. C. P., & Nestler, E. J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500587102 · Cited by 162 · see citing works

Role of nucleus accumbens in neuropathic pain: Linked multi-scale evidence in the rat transitioning to neuropathic pain

Chang, P.-C., Pollema-Mays, S. L., Centeno, M. V., Procissi, D., Contini, M., Baria, A. T., Martina, M., & Apkarian, A. V. (2014) · Pain · doi:10.1016/j.pain.2014.02.019 · Cited by 161 · see citing works

Natural Addiction

Hoebel, B. G., Avena, N. M., Bocarsly, M. E., & Rada, P. V. (2009) · Journal of Addiction Medicine · doi:10.1097/adm.0b013e31819aa621 · Cited by 159 · see citing works

Feelings about food: the ventral tegmental area in food reward and emotional eating

Meye, F. J., & Adan, R. A. H. (2013) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2013.11.003 · Cited by 156 · see citing works

Neuroimaging for drug addiction and related behaviors

Parvaz, M. A., Alia-Klein, N., Woicik, P. A., Volkow, N. D., & Goldstein, R. Z. (2011) · Reviews in the Neurosciences · doi:10.1515/rns.2011.055 · Cited by 151 · see citing works

Parceling Human Accumbens into Putative Core and Shell Dissociates Encoding of Values for Reward and Pain

Baliki, M. N., Mansour, A. R., Baria, A. T., Huang, L., Berger, S., Fields, H. L., & Apkarian, A. V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1731-13.2013 · Cited by 146 · see citing works

Phasic Nucleus Accumbens Dopamine Encodes Risk-Based Decision-Making Behavior

Sugam, J. A., Day, J. J., Wightman, R. M., & Carelli, R. M. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.09.029 · Cited by 142 · see citing works

Stress responses and the mesolimbic dopamine system: Social contexts and sex differences

Trainor, B. C. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.08.013 · Cited by 138 · see citing works

Architectural Representation of Valence in the Limbic System

Namburi, P., Al‐Hasani, R., Calhoon, G. G., Bruchas, M. R., & Tye, K. M. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.358 · Cited by 133 · see citing works

A Role for Phasic Dopamine Release within the Nucleus Accumbens in Encoding Aversion: A Review of the Neurochemical Literature

Wenzel, J. M., Rauscher, N. A., Cheer, J. F., & Oleson, E. B. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn500255p · Cited by 131 · see citing works

Stress-induced anhedonia is associated with hypertrophy of medium spiny neurons of the nucleus accumbens

Bessa, J. M., Morais, M., Marques, F., Pinto, L., Palha, J. A., Almeida, O. F. X., & Sousa, N. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.39 · Cited by 130 · see citing works

Highly processed foods can be considered addictive substances based on established scientific criteria

Gearhardt, A. N., & DiFeliceantonio, A. G. (2022) · Addiction · doi:10.1111/add.16065 · Cited by 128 · see citing works

Induction of Hyperphagia and Carbohydrate Intake by μ-Opioid Receptor Stimulation in Circumscribed Regions of Frontal Cortex

Mena, J. D., Sadeghian, K., & Baldo, B. A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2050-10.2011 · Cited by 125 · see citing works

Glucagon-Like Peptide-1 Receptor Activation in the Nucleus Accumbens Core Suppresses Feeding by Increasing Glutamatergic AMPA/Kainate Signaling

Mietlicki‐Baase, E. G., Ortinski, P. I., Reiner, D. J., Sinon, C. G., McCutcheon, J. E., Pierce, R. C., Roitman, M. F., & Hayes, M. R. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0115-14.2014 · Cited by 122 · see citing works

Differential neurochemical and behavioral adaptation to cocaine after response contingent and noncontingent exposure in the rat

Lecca, D., Cacciapaglia, F., Valentini, V., Acquas, E., & Chiara, G. D. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0496-y · Cited by 121 · see citing works

From Malthus to motive: How the HPA axis engineers the phenotype, yoking needs to wants

Pecoraro, N. C., Dallman, M. F., Warne, J. P., Ginsberg, A. B., Laugero, K. D., la Fleur, S. E., Houshyar, H., Gómez-Oliver, F., Bhargava, A., & Akana, S. F. (2006) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2006.07.004 · Cited by 120 · see citing works

Toward an integrative model of the spectrum of mood, behavioral and personality disorders based on fear and anger traits: I. Clinical implications

Lara, D. R., Pinto, O., Akiskal, K. K., & Akiskal, H. H. (2006) · Journal of Affective Disorders · doi:10.1016/j.jad.2006.02.025 · Cited by 119 · see citing works

Social, clinical, and policy implications of ultra-processed food addiction

Gearhardt, A. N., Bueno, N. B., DiFeliceantonio, A. G., Roberto, C. A., Jiménez‐Múrcia, S., & Fernández‐Aranda, F. (2023) · BMJ · doi:10.1136/bmj-2023-075354 · Cited by 127 · see citing works

Energy regulatory signals and food reward

Figlewicz, D. P., & Sipols, A. J. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.03.002 · Cited by 111 · see citing works

Topography of Reward and Aversion Encoding in the Mesolimbic Dopaminergic System

Yuan, L., Dou, Y., & Sun, Y.-G. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0271-19.2019 · Cited by 108 · see citing works

Operant Sensation Seeking Engages Similar Neural Substrates to Operant Drug Seeking in C57 Mice

Olsen, C. M., & Winder, D. G. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2008.226 · Cited by 111 · see citing works

Dopamine, Prediction Error and Beyond

Diederen, K. M. J., & Fletcher, P. C. (2021) · The Neuroscientist · doi:10.1177/1073858420907591 · Cited by 106 · see citing works

The Human Nucleus Accumbens: Where Is It? A Stereotactic, Anatomical and Magnetic Resonance Imaging Study

Neto, L. L., Oliveira, E., Correia, F., & Gonçalves-Ferreira, A. (2008) · Neuromodulation Technology at the Neural Interface · doi:10.1111/j.1525-1403.2007.00138.x · Cited by 105 · see citing works

Does the kappa opioid receptor system contribute to pain aversion?

Cahill, C. M., Taylor, A. M. W., Cook, C., Ong, E., Morón, J. A., & Evans, C. J. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00253 · Cited by 105 · see citing works

Smile and laughter induction and intraoperative predictors of response to deep brain stimulation for obsessive-compulsive disorder

Haq, I. U., Foote, K. D., Goodman, W. G., Wu, S. S., Sudhyadhom, A., Ricciuti, N., Siddiqui, M., Bowers, D., Jacobson, C. E., Ward, H. E., et al. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.03.009 · Cited by 105 · see citing works

Endocannabinoid modulation of homeostatic and non-homeostatic feeding circuits

Lau, B. K., Cota, D., Cristino, L., & Borgland, S. L. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.05.033 · Cited by 102 · see citing works

Dopamine tunes prefrontal outputs to orchestrate aversive processing

Weele, C. M. V., Siciliano, C. A., & Tye, K. M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.11.044 · Cited by 89 · see citing works

Withdrawal from free-choice high-fat high-sugar diet induces craving only in obesity-prone animals

Pickering, C., Alsiö, J., Hulting, A., & Schiöth, H. B. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1474-y · Cited by 91 · see citing works

Cannabinoid facilitation of behavioral and biochemical hedonic taste responses

Luca, M. A. D., Solinas, M., Bimpisidis, Z., Goldberg, S. R., & Chiara, G. D. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.10.018 · Cited by 91 · see citing works

An in vivo profile of β-endorphin release in the arcuate nucleus and nucleus accumbens following exposure to stress or alcohol

Marinelli, P. W., Quirion, R., & Gianoulakis, C. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.05.047 · Cited by 103 · see citing works

Activation of dopamine D1‐like receptors in nucleus accumbens is critical for the acquisition, but not the expression, of nutrient‐conditioned flavor preferences in rats

Touzani, K., Bodnar, R. J., & Sclafani, A. J. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06127.x · Cited by 84 · see citing works

Alterations in food intake by opioid and dopamine signaling pathways between the ventral tegmental area and the shell of the nucleus accumbens

MacDonald, A. F., Billington, C. J., & Levine, A. S. (2004) · Brain Research · doi:10.1016/j.brainres.2004.05.043 · Cited by 83 · see citing works

Mesolimbic dopaminergic activity responding to acute stress is blunted in adolescent rats that experienced neonatal maternal separation

Jahng, J. W., Ryu, V., Yoo, S. B., Noh, S. J., Kim, J. Y., & Lee, J. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.08.063 · Cited by 82 · see citing works

Dopamine and learned food preferences

Sclafani, A. J., Touzani, K., & Bodnar, R. J. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.04.039 · Cited by 83 · see citing works

Taste pathways that mediate accumbens dopamine release by sapid sucrose

Hajnal, A., & Norgren, R. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.12.014 · Cited by 80 · see citing works

Defining the Caudal Ventral Striatum in Primates: Cellular and Histochemical Features

Fudge, J. L., & Haber, S. N. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-23-10078.2002 · Cited by 79 · see citing works

Individual differences in response to positive and negative stimuli: endocannabinoid-based insight on approach and avoidance behaviors

Laricchiuta, D., & Petrosini, L. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00238 · Cited by 80 · see citing works

Rewarding and aversive effects of nicotine are segregated within the nucleus accumbens

Sellings, L. H. L., Baharnouri, G., McQuade, L. E., & Clarke, P. B. S. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06341.x · Cited by 76 · see citing works

Dopamine and monogamy

Curtis, J. T., Liu, Y., Aragona, B. J., & Wang, Z. (2006) · Brain Research · doi:10.1016/j.brainres.2006.07.126 · Cited by 74 · see citing works

Dopamine and Food Addiction: Lexicon Badly Needed

Salamone, J. D., & Correa, M. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.027 · Cited by 71 · see citing works

Dual Role of Medial A10 Dopamine Neurons in Affective Encoding

Liu, Z., Shin, R. S., & Ikemoto, S. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.4 · Cited by 73 · see citing works

Weighing in the Role of BDNF in the Central Control of Eating Behavior

Cordeira, J., & Rios, M. (2011) · Molecular Neurobiology · doi:10.1007/s12035-011-8212-2 · Cited by 72 · see citing works

Differential impact of pavlovian drug conditioned stimuli on in vivo dopamine transmission in the rat accumbens shell and core and in the prefrontal cortex

Bassareo, V., Luca, M. A. D., & Chiara, G. D. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0560-7 · Cited by 71 · see citing works

Reciprocal effects of response contingent and noncontingent intravenous heroin on in vivo nucleus accumbens shell versus core dopamine in the rat: a repeated sampling microdialysis study

Lecca, D., Valentini, V., Cacciapaglia, F., Acquas, E., & Chiara, G. D. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0815-y · Cited by 70 · see citing works

An animal model of eating disorders associated with stressful experience in early life

Jahng, J. W. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.11.010 · Cited by 70 · see citing works

Postnatal Aversive Experience Impairs Sensitivity to Natural Rewards and Increases Susceptibility to Negative Events in Adult Life

Ventura, R., Coccurello, R., Andolina, D., Latagliata, E. C., Zanettini, C., Lampis, V., Battaglia, M., D'Amato, F. R., & Moles, A. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs145 · Cited by 68 · see citing works

Representation of Subjective Value in the Striatum

Knutson, B. D., Delgado, M. R., & Phillips, P. E. M. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374176-9.00025-7 · Cited by 68 · see citing works

Nucleus accumbens core and shell inactivation differentially affects impulsive behaviours in rats

Feja, M., Hayn, L., & Koch, M. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.04.012 · Cited by 65 · see citing works

Differential adaptive properties of accumbens shell dopamine responses to ethanol as a drug and as a motivational stimulus

Bassareo, V., Luca, M. A. D., Aresu, M., Aste, A., Ariu, T., & Chiara, G. D. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02556.x · Cited by 66 · see citing works

Suppression by the cannabinoid CB1 receptor antagonist, rimonabant, of the reinforcing and motivational properties of a chocolate-flavoured beverage in rats

Maccioni, P., Pes, D., Carai, M. A. M., Gessa, G. L., & Colombo, G. (2008) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e3282fe8888 · Cited by 65 · see citing works

Acquisition of a palatable-food-sustained appetitive behavior in satiated rats is dependent on the dopaminergic response to this food in limbic areas

Gambarana, C., Masi, F., Leggio, B., Grappi, S., Nanni, G., Scheggi, S., Montis, M. G. D., & Tagliamonte, A. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00383-x · Cited by 62 · see citing works

Dopamine efflux in nucleus accumbens shell and core in response to appetitive classical conditioning

Cheng, J., de Bruin, J. P. C., & Feenstra, M. G. P. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02849.x · Cited by 62 · see citing works

Cannabinoid-induced Fos expression within A10 dopaminergic neurons

Patel, S., & Hillard, C. J. (2003) · Brain Research · doi:10.1016/s0006-8993(02)03797-6 · Cited by 61 · see citing works

Forebrain c-fos expression under conditions conducive to pair bonding in female prairie voles (Microtus ochrogaster)

Curtis, J. T., & Wang, Z. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00226-9 · Cited by 61 · see citing works

High frequency stimulation of the subthalamic nucleus modulates neurotransmission in limbic brain regions of the rat

Winter, C., Lemke, C., Sohr, R., Meissner, W. G., Harnack, D., Juckel, G., Morgenstern, R., & Kupsch, A. R. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-1171-1 · Cited by 60 · see citing works

Intravascular Food Reward

Oliveira-Maia, A. J., Roberts, C. D., Walker, Q. D., Luo, B., Kuhn, C. M., Simon, S. A., & Nicolelis, M. A. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024992 · Cited by 58 · see citing works

Distinct kinds of novelty processing differentially increase extracellular dopamine in different brain regions

De Leonibus, E., Verheij, M. M. M., Mele, A., & Cools, A. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04658.x · Cited by 57 · see citing works

Neuropharmacology of learned flavor preferences

Touzani, K., Bodnar, R. J., & Sclafani, A. J. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.06.001 · Cited by 57 · see citing works

Dopamine responsiveness in Nucleus Accumbens Shell and Core and Prefrontal Cortex during operant behavior for sucrose

Cucca, F. (2014) · VEprints - Universita degli Studi di Cagliari

Accumbal shell and core dopamine responsiveness during operant responding for sucrose

Bassareo, V., Musio, P., Lecca, D., & Chiara, G. D. (2010) · UNICA IRIS Institutional Research Information System (University of Cagliari)

NUCLEUS ACCUMBENS SHELL AND CORE DOPAMINE MODIFICATIONS DURING OPERANT RESPONDING FOR SUCROSE

Bassareo, V., Cucca, F., Musio, P., Lecca, D., Frau, R., & Chiara, G. D. (2014) · UNICA IRIS Institutional Research Information System (University of Cagliari)

Nucleus Accumbens and Prefrontal Cortex Dopamine modifications during operant responding for sucrose

Bassareo, V., Musio, P., Cucca, F., & Chiara, G. D. (2011) · UNICA IRIS Institutional Research Information System (University of Cagliari)

Adaptive changes of dopamine responsiveness to palatable food: differences between accumbens shell, core and prefrontal cortex

Bassareo, V., & Chiara, G. D. (2008) · UNICA IRIS Institutional Research Information System (University of Cagliari)