The DOI matches its Crossref record; 103 of the 103 references it cites were found in a registry or an index.
What and when to "want"? Amygdala-based focusing of incentive salience upon sugar and sex
Open accessAbstract
Rationale Amygdala-related circuitry helps translate learned Pavlovian associations into appetitive and aversive motivation, especially upon subsequent encounters with cues. Objectives We asked whether μ-opioid stimulation via microinjections of the specific agonist D-Ala(2), N-MePhe(4), Gly-ol)-enkephalin (DAMGO) in central nucleus of amygdala (CeA), or the adjacent basolateral amygdala (BLA) would magnify sucrose or sex "wanting", guided by available cues. Materials and methods CeA or BLA DAMGO enhancement of cue-triggered "wanting" was assessed using Pavlovian to instrumental transfer (PIT). Unconditioned food "wanting" was measured via intake, and male sexual "wanting" for an estrous female was measured in a sexual approach test. Sucrose hedonic taste "liking" was measured in a taste reactivity test. Results CeA (but not BLA) DAMGO increased the intensity of phasic peaks in instrumental sucrose seeking stimulated by Pavlovian cues over precue levels in PIT, while suppressing seeking at other moments. CeA DAMGO also enhanced food intake, as well as sexual approach and investigation of an estrous female by males. DAMGO "wanting" enhancements were localized to CeA, as indicated by "Fos plume"-based anatomical maps for DAMGO causation of behavioral effects. Despite increasing "wanting", CeA DAMGO decreased the hedonic impact or "liking" for sucrose in a taste reactivity paradigm. Conclusions CeA μ-opioid stimulation specifically enhances incentive salience, which is dynamically guided to food or sex by available cues.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Evidence suggests that repeated excitation by sexual stimuli can have a similar effect (Lynch and Ryan, 2020;Mahler and Berridge, 2012).”
From A motivation model of sex addiction – Relevance to the controversy over the concept (2022) · cites this paper as Mahler and Berridge, 2012
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444
The neural basis of drug craving: An incentive-sensitization theory of addiction
Robinson, T. (1993) · Brain Research Reviews · doi:10.1016/0165-0173(93)90013-p · Cited by 7,346
AChE-stained horizontal sections of the rat brain in stereotaxic coordinates
Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,514
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
Self-citationIntegrative activity of the brain
Konorski, J. (1967) · University of Chicago Press eBooks · Cited by 2,043
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 1,220
A selective role for dopamine in stimulus-reward learning
Flagel, S. B., Clark, J. J., Robinson, T. E., Mayo, L., Czuj, A., Willuhn, I., Akers, C. A., Clinton, S. M., Phillips, P. E. M., & Akil, H. (2011) · Nature · doi:10.1038/nature09588 · Cited by 1,026
The Amygdala: a functional analysis
Aggleton, J. P. (2000) · Cited by 966
Research works printed but not linked: 3
- Difeliceantonio AG, Berridge KC (2010) Neostriatal sites of mu opioid stimulation enhance CS motivational magnets. Society for Neuroscience, San Diego, CA
- Peciña S, Berridge KC (2008) Incentive salience mediation by opioid versus dopamine in nucleus accumbens shell and core: amplified cue-triggered ‘wanting’ for reward Society for Neuroscience. Society for Neuroscience, Washington, DC
- Toates F (1986) Motivational Systems. Cambridge University Press, Cambridge, UK
Cited by
Sorted by citations
Berridge, K. C., & Kringelbach, M. L. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.018 · Cited by 1,730
Self-citationFrom prediction error to incentive salience: mesolimbic computation of reward motivation.
Berridge, K. C. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.07990.x · Cited by 700
Self-citationNeuroscience of affect: brain mechanisms of pleasure and displeasure
Berridge, K. C., & Kringelbach, M. L. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.01.017 · Cited by 532
Self-citationCastro, D. C., & Berridge, K. C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4458-13.2014 · Cited by 395
Self-citationModel-based and model-free Pavlovian reward learning: Revaluation, revision, and revelation
Dayan, P., & Berridge, K. C. (2014) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-014-0277-8 · Cited by 357
Self-citation“Liking” and “wanting” in eating and food reward: Brain mechanisms and clinical implications
Morales, I., & Berridge, K. C. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113152 · Cited by 346
Self-citationMaier, S. U., Makwana, A. B., & Hare, T. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.005 · Cited by 270
Measuring wanting and liking from animals to humans: a systematic review
Pool, E., Sennwald, V., Delplanque, S., Brosch, T., & Sander, D. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.01.006 · Cited by 211
Rewards of beauty: the opioid system mediates social motivation in humans
Chelnokova, O., Laeng, B., Eikemo, M., Riegels, J., Løseth, G. E., Maurud, H., Willoch, F., & Leknes, S. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.1 · Cited by 199
Ellingsen, D., Leknes, S., Løseth, G. E., Wessberg, J., & Olausson, H. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01986 · Cited by 214
Politis, M., Loane, C., Wu, K., O’Sullivan, S. S., Woodhead, Z., Kiferle, L., Lawrence, A. D., Lees, A. J., & Piccini, P. (2013) · Brain · doi:10.1093/brain/aws326 · Cited by 191
Mapping brain circuits of reward and motivation: In the footsteps of Ann Kelley
Richard, J. M., Castro, D. C., DiFeliceantonio, A. G., Robinson, M. J. F., & Berridge, K. C. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.12.008 · Cited by 183
Self-citationInfluence of reward motivation on human declarative memory
Lombard, E., Bavelier, D., & Schwartz, S. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.11.015 · Cited by 191
Basolateral amygdala to orbitofrontal cortex projections enable cue-triggered reward expectations
Lichtenberg, N. T., Pennington, Z. T., Holley, S. M., Greenfield, V. Y., Cepeda, C., Levine, M. S., & Wassum, K. M. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.0486-17.2017 · Cited by 171
The Central Amygdala Nucleus is Critical for Incubation of Methamphetamine Craving
Li, X., Zeric, T., Kambhampati, S., Bossert, J. M., & Shaham, Y. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.320 · Cited by 163
Advances in the neurobiological bases for food ‘liking’ versus ‘wanting’
Castro, D. C., & Berridge, K. C. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.05.022 · Cited by 175
Self-citationCurrent perspectives on incentive salience and applications to clinical disorders
Olney, J. J., Warlow, S. M., Naffziger, E. E., & Berridge, K. C. (2018) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2018.01.007 · Cited by 157
Self-citationDiFeliceantonio, A. G., & Berridge, K. C. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.02.032 · Cited by 141
Self-citationDifferential effects of acute stress on anticipatory and consummatory phases of reward processing
Kumar, P., Berghorst, L. H., Nickerson, L. D. H., Dutra, S. J., Goer, F., Greve, D. N., & Pizzagalli, D. A. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.058 · Cited by 146
Enkephalin Surges in Dorsal Neostriatum as a Signal to Eat
DiFeliceantonio, A. G., Mabrouk, O. S., Kennedy, R. T., & Berridge, K. C. (2012) · Current Biology · doi:10.1016/j.cub.2012.08.014 · Cited by 131
Self-citationState-dependent μ-opioid modulation of social motivation
Løseth, G. E., Ellingsen, D., & Leknes, S. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00430 · Cited by 128
The role of the opioid system in decision making and cognitive control: a review
van Steenbergen, H., Eikemo, M., & Leknes, S. (2019) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-019-00710-6 · Cited by 118
Mahler, S. V., Brodnik, Z. D., Cox, B. M., Buchta, W. C., Bentzley, B. S., Quintanilla, J., Cope, Z. A., Lin, E. C., Riedy, M. D., Scofield, M. D., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0537-18.2018 · Cited by 104
Self-citationEndogenous opiates and behavior: 2012
Bodnar, R. J. (2013) · Peptides · doi:10.1016/j.peptides.2013.10.001 · Cited by 98
Meyer, P., Cogan, E. S., & Robinson, T. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098163 · Cited by 94
Sweet taste pleasantness is modulated by morphine and naltrexone
Eikemo, M., Løseth, G. E., Johnstone, T., Gjerstad, J., Willoch, F., & Leknes, S. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4403-x · Cited by 92
Bolton, J. L., Ruiz, C. M., Rismanchi, N., Sanchez, G. A., Castillo, E., Huang, J. J., Cross, C., Baram, T. Z., & Mahler, S. V. (2018) · Neurobiology of Stress · doi:10.1016/j.ynstr.2018.01.002 · Cited by 93
Self-citationRole of central amygdala neuronal ensembles in incubation of nicotine craving
Funk, D., Coen, K., Tamadon, S., Hope, B. T., Shaham, Y., & Lê, A. D. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1505-16.2016 · Cited by 87
Suardi, A. C., Sotgiu, I., Costa, T., Cauda, F., & Rusconi, M. L. (2016) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-016-0414-7 · Cited by 91
Food Addiction and Binge Eating: Lessons Learned from Animal Models
Novelle, M. G., & Diéguez, C. (2018) · Nutrients · doi:10.3390/nu10010071 · Cited by 90
The effects of Beta-Endorphin: state change modification
Veening, J. G., & Barendregt, H. P. (2015) · Fluids and Barriers of the CNS · doi:10.1186/2045-8118-12-3 · Cited by 89
Is comfort food really comforting? Mechanisms underlying stress-induced eating
Pool, E. R., Delplanque, S., Coppin, G., & Sander, D. (2015) · Food Research International · doi:10.1016/j.foodres.2014.12.034 · Cited by 87
Optogenetic activation of the central amygdala generates addiction‐like preference for reward
Tom, R. L., Ahuja, A., Maniates, H., Freeland, C. M., & Robinson, M. J. F. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13967 · Cited by 78
Incentive motivation: ‘wanting’ roles of central amygdala circuitry
Warlow, S. M., & Berridge, K. C. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113376 · Cited by 84
Self-citationDiFeliceantonio, A. G., & Berridge, K. C. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13220 · Cited by 69
Self-citationThe central amygdala recruits mesocorticolimbic circuitry for pursuit of reward or pain
Warlow, S. M., Naffziger, E. E., & Berridge, K. C. (2020) · Nature Communications · doi:10.1038/s41467-020-16407-1 · Cited by 79
Self-citationPfaus, J. G., Jones, S. L., Flanagan‐Cato, L. M., & Blaustein, J. D. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397175-3.00050-8 · Cited by 73
Prefrontal/accumbal catecholamine system processes high motivational salience
Puglisi‐Allegra, S., & Ventura, R. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00031 · Cited by 71
The Cambridge Handbook of Substance and Behavioral Addictions
Sussman, S. Y. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591 · Cited by 64
Reichelt, A. C., Westbrook, R. F., & Morris, M. J. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13321 · Cited by 62
Motivational Processes Underlying Substance Abuse Disorder
Meyer, P., King, C. P., & Ferrario, C. R. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2015_391 · Cited by 59
Opendak, M. M., Robinson-Drummer, P. A., Blomkvist, A., Zanca, R. M., Wood, K., Jacobs, L., Chan, S., Tan, S., Woo, J., Venkataraman, G., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0340-9 · Cited by 56
The Virtual Personalities Neural Network Model: Neurobiological Underpinnings
Read, S. J., Brown, A. D., Wang, P., & Miller, L. C. (2018) · Personality Neuroscience · doi:10.1017/pen.2018.6 · Cited by 55
Positive emotions have a unique capacity to capture attention
Gupta, R. (2019) · Progress in brain research · doi:10.1016/bs.pbr.2019.02.001 · Cited by 64
Pelloux, Y., Minier-Toribio, A. M., Hoots, J. K., Bossert, J. M., & Shaham, Y. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2521-17.2017 · Cited by 55
Stress, Motivation, and the Gut–Brain Axis: A Focus on the Ghrelin System and Alcohol Use Disorder
Morris, L. S., Voon, V., & Leggio, L. (2018) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13781 · Cited by 57
Baldo, B. A., Pratt, W. E., Will, M. J., Hanlon, E. C., Bakshi, V. P., & Cador, M. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.02.017 · Cited by 57
Imaging the neural effects of cognitive bias modification training
Wiers, C. E., & Wiers, R. W. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.07.041 · Cited by 52
Laeng, B., Garvija, L. K., Løseth, G. E., Eikemo, M., Ernst, G., & Leknes, S. (2021) · Consciousness and Cognition · doi:10.1016/j.concog.2021.103105 · Cited by 54
Reed, D. D., Naudé, G. P., Gelino, B. W., & Amlung, M. T. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.011 · Cited by 48
Litman, J. A. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316823279.019 · Cited by 49
Growing pains and pleasures: how emotional learning guides development
Nelson, E. E., Lau, J. Y. F., & Jarcho, J. M. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.11.003 · Cited by 48
Activation of basolateral amygdala in juvenile C57BL/6J mice during social approach behavior
Ferri, S. L., Kreibich, A. S., Torre, M., Piccoli, C. T., Dow, H. C., Pallathra, A. A., Li, H., Bilker, W. B., Gur, R. C., Abel, T. G., et al. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.08.006 · Cited by 48
The incentive salience of courtship vocalizations: Hormone-mediated ‘wanting’ in the auditory system
Maney, D. L. (2013) · Hearing Research · doi:10.1016/j.heares.2013.04.011 · Cited by 47
The Prevention and Treatment of Gambling Disorders: Some Art, Some Science
Derevensky, J. L. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.024 · Cited by 45
Food intake and addictive-like eating behaviors: Time to think about the circadian clock(s)
Mendoza, J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.07.003 · Cited by 50
The role of the opioid system in binge eating disorder
Giuliano, C., & Cottone, P. (2015) · CNS Spectrums · doi:10.1017/s1092852915000668 · Cited by 45
Considering the Overlap and Nonoverlap of Compulsivity, Impulsivity, and Addiction
Blum, A. W., & Grant, J. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.038 · Cited by 44
Neurobiological Foundations of Behavioral Addictions
Vaccaro, A. G., & Potenza, M. N. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.016 · Cited by 45
Neurobiology of Substance Addictions
Christie, N. C., & Bechara, A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.015 · Cited by 44
Sensitization of Incentive Salience and the Transition to Addiction
Warlow, S. M., Baumgartner, H. M., Freeland, C. M., Naffziger, E. E., Olney, J. J., Berridge, K. C., & Robinson, M. J. F. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.006 · Cited by 46
Self-citationMindfulness-Based Interventions Applied to Addiction Treatments
Kechter, A., & Black, D. S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.040 · Cited by 43
Multiple Memory Systems, Addiction, and Health Habits: New Routes for Translational Science
Stacy, A. W., Pike, J. R., & Lee, A. Y. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.017 · Cited by 43
Tanning as an Addiction: The State of the Research and Implications for Intervention
Miller, K. A., & Mays, D. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.037 · Cited by 43
Schulte, E. M., Schiestl, E. T., & Gearhardt, A. N. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.035 · Cited by 43
Behavioral Economics and Addictive Disorders
Jarmolowicz, D. P., & Schneider, T. D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.005 · Cited by 42
Prevention and Treatment of Compulsive Buying Disorder
Galimov, A., & Black, D. W. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.027 · Cited by 42
Blum, K., Roy, A. K., Podesta, A., Modestino, E. J., Steinberg, B., Gondré-Lewis, M. C., Baron, D. A., Thanos, P. K., Lott, L., Badgaiyan, S., et al. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.031 · Cited by 42
Prevention and Treatment of “Food Addiction”
Davis, C., & Mason, A. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.023 · Cited by 42
Human Neurobiological Approaches to Hedonically Motivated Behaviors
Burger, K. S., Shearrer, G. E., & Sadler, J. R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.009 · Cited by 42
Feedback Models for Gambling Control: The Use and Efficacy of Online Responsible Gambling Tools
Griffiths, M. D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.034 · Cited by 42
Enduring disruption of reward and stress circuit activities by early-life adversity in male rats
Levis, S. C., Birnie, M. T., Bolton, J. L., Perrone, C. R., Montesinos, J. S., Baram, T. Z., & Mahler, S. V. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01988-w · Cited by 44
Self-citationEmotional attention for erotic stimuli: Cognitive and brain mechanisms
Sennwald, V., Pool, E. R., Brosch, T., Delplanque, S., Bianchi‐Demicheli, F., & Sander, D. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23859 · Cited by 42
Naneix, F., Darlot, F., Coutureau, É., & Cador, M. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13149 · Cited by 43
Bodnar, R. J. (2019) · Peptides · doi:10.1016/j.peptides.2019.04.008 · Cited by 40
Opioid Modulation of Value-Based Decision-Making in Healthy Humans
Eikemo, M., Biele, G., Willoch, F., Thomsen, L., & Leknes, S. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.58 · Cited by 39
Sucrose intake lowers μ-opioid and dopamine D2/3 receptor availability in porcine brain
Winterdahl, M., Noer, O., Orłowski, D., Schacht, A. C., Jakobsen, S., Alstrup, A. K. O., GJEDDE, A. H., & Landau, A. M. (2019) · Scientific Reports · doi:10.1038/s41598-019-53430-9 · Cited by 43
Mitchell, M. R., Berridge, K. C., & Mahler, S. V. (2018) · Cannabis and Cannabinoid Research · doi:10.1089/can.2018.0021 · Cited by 36
“Microinjections of the endogenous cannabinoid anandamide, or specific l opioid agonists, when centered in the hotspot region, robustly enhance sucrose ‘‘liking’’.(20,29) We show in this study that for anandamide microinjection to enhance hedonics, endogenous signaling at opioid receptors is required, as coadministrati…”
BackgroundMethodSelf-citationStress and reward processing in bipolar disorder: a functional magnetic resonance imaging study
Berghorst, L. H., Kumar, P., Greve, D. N., Deckersbach, T., Öngür, D., Dutra, S. J., & Pizzagalli, D. A. (2016) · Bipolar Disorders · doi:10.1111/bdi.12444 · Cited by 37
Selleck, R. A., & Baldo, B. A. (2017) · Psychopharmacology · doi:10.1007/s00213-016-4522-4 · Cited by 34
Separating desire from prediction of outcome value
Berridge, K. C. (2023) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2023.07.007 · Cited by 37
Self-citationLøseth, G. E., Eikemo, M., & Leknes, S. (2019) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsz022 · Cited by 28
Chang, L., Kigar, S. L., Ho, J. H., Cuarenta, A., Gunderson, H. C., Baldo, B. A., Bakshi, V. P., & Auger, A. P. (2018) · Brain Research · doi:10.1016/j.brainres.2018.12.040 · Cited by 33
The Developmental Origins of Opioid Use Disorder and Its Comorbidities
Levis, S. C., Mahler, S. V., & Baram, T. Z. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.601905 · Cited by 33
Self-citationAmygdala mu‐opioid receptors mediate the motivating influence of cue‐triggered reward expectations
Lichtenberg, N. T., & Wassum, K. M. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13477 · Cited by 29
Endogenous central amygdala mu-opioid receptor signaling promotes sodium appetite in mice
Smith, C. M., Walker, L., Leeboonngam, T., McKinley, M. J., Denton, D. A., & Lawrence, A. J. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1616664113 · Cited by 26
A motivation model of sex addiction – Relevance to the controversy over the concept
Toates, F. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104872 · Cited by 25
“Evidence suggests that repeated excitation by sexual stimuli can have a similar effect (Lynch and Ryan, 2020; Mahler and Berridge, 2012).”
BackgroundThe Use of Functional Magnetic Resonance Imaging in the Study of Appetite and Obesity
Neseliler, S., Han, J.-E., & Dagher, A. (2017) · CRC Press eBooks · doi:10.1201/9781315120171-6 · Cited by 26
The Central Extended Amygdala Guides Survival-Relevant Tradeoffs for Action SelectionPreprint
Holley, D., & Fox, A. S. (2022) · PsyArXiv (OSF Preprints) · doi:10.1016/j.neubiorev.2022.104879 · Cited by 23
Association between reward-related functional connectivity and tri-level mood and anxiety symptoms
Anderson, Z. G., Damme, K. S. F., Carroll, A., Chat, I. K.-Y., Young, K. S., Craske, M. G., Bookheimer, S. Y., Zinbarg, R. E., & Nusslock, R. (2023) · NeuroImage Clinical · doi:10.1016/j.nicl.2023.103335 · Cited by 26
Reis, H. S., Rodrigues, I. R. S., Anjos-Santos, A., Libarino-Santos, M., Serra, Y. A., Cata-Preta, E. G., Oliveira-Campos, D., Kisaki, N. D., Barros-Santos, T., Yokoyama, T. S., et al. (2020) · Psychopharmacology · doi:10.1007/s00213-020-05609-6 · Cited by 21
Ross, S. E., Levin, E. L., Itoga, C. A., Schoen, C. B., Selmane, R., & Aldridge, J. W. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13342 · Cited by 21
Reichard, R. A., Subramanian, S., Desta, M. T., Sura, T. A., Becker, M. L., Ghobadi, C. W., Parsley, K. P., & Zahm, D. S. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1321-y · Cited by 23
Björk, K., Tronci, V., Thorsell, A., Tanda, G., Hirth, N., Heilig, M. A., Hansson, A. C., & Sommer, W. H. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3166-x · Cited by 19
Transforming experiences: Neurobiology of memory updating/editing
Osorio‐Gómez, D., Miranda, M. I., Guzmán-Ramos, K. R., & Bermúdez‐Rattoni, F. (2023) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2023.1103770 · Cited by 20
Bodnar, R. J. (2015) · Peptides · doi:10.1016/j.peptides.2015.03.019 · Cited by 18
Salt Appetite, and the Influence of Opioids
Smith, C. M., & Lawrence, A. J. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2336-3 · Cited by 18
Sebold, M., Garbusow, M., Cerci, D., Chen, K., Sommer, C., Huys, Q. J. M., Nebe, S., Rapp, M. A., Veer, I. M., Zimmermann, U. S., et al. (2021) · Journal of Psychopharmacology · doi:10.1177/0269881121991992 · Cited by 17
Opioid Regulation of Social Homeostasis: Connecting Loneliness to Addiction
Løseth, G. E., Eikemo, M., & Leknes, S. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.11.011 · Cited by 16
Ravindranath, O., Ordaz, S. J., Padmanabhan, A., Foran, W., Jalbrzikowski, M., Calabro, F. J., & Luna, B. (2020) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2020.100836 · Cited by 14
Metadata
- Authors
- Mahler, S. V., & Berridge, K. C.
- Affiliations
- Medical University of South Carolina (US)
- University of Michigan (US)
- Corresponding author
- Mahler, Stephen V.
- Venue
- Psychopharmacology
- Published
- 2011-12-14
- Volume
- 221
- Issue
- 3
- Pages
- 407-426
- ISSN
- 0033-3158 (ISSN-L)
- 1432-2072
- PMC
- PMC3444284
- OpenAlex
- W2147423572
- Cited by
- 170
- References
- 103
- Citations by year
- 2026: 6 · 2025: 3 · 2024: 2 · 2023: 5 · 2022: 7 · 2021: 6 · 2020: 49 · 2019: 14 · 2018: 14 · 2017: 9 · 2016: 18 · 2015: 12 · 2014: 11 · 2013: 6 · 2012: 8
- FWCI
- 3.13
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Psychopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (1s15mh053649-01)
- National Institute of Mental Health (MH053649, R01MH063649)
- National Institute on Drug Abuse (DA021481, DA015188, R01DA015188, F31DA021481)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- central amygdala, basolateral amygdala, mu-opioid receptor, DAMGO, incentive salience, sexual motivation, Pavlovian-to-instrumental transfer, sucrose seeking, dietary intake
- MeSH terms
- Amygdala, Analgesics, Opioid, Animals, Behavior, Animal, Cues, Eating, Estrus, Female, Male, Sexual Behavior, Animal, Sucrose, Rats, Sprague-Dawley, Receptors, Opioid, mu, Enkephalin, Ala(2)-MePhe(4)-Gly(5)-, 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