The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
Sucrose activates human taste pathways differently from artificial sweetener
Abstract
Animal models suggest that sucrose activates taste afferents differently than non-caloric sweeteners. Little information exists how artificial sweeteners engage central taste pathways in the human brain. We assessed sucrose and sucralose taste pleasantness across a concentration gradient in 12 healthy control women and applied 10% sucrose and matched sucralose during functional magnet resonance imaging. The results indicate that (1) both sucrose and sucralose activate functionally connected primary taste pathways; (2) taste pleasantness predicts left insula response; (3) sucrose elicits a stronger brain response in the anterior insula, frontal operculum, striatum and anterior cingulate, compared to sucralose; (4) only sucrose, but not sucralose, stimulation engages dopaminergic midbrain areas in relation to the behavioral pleasantness response. Thus, brain response distinguishes the caloric from the non-caloric sweetener, although the conscious mind could not. This could have important implications on how effective artificial sweeteners are in their ability to substitute sugar intake.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Human imaging studies have shown that tasting palatable foods activated the insula and midbrain areas (143,144).”
From Obesity and addiction: Neurobiological overlaps (2013) · cites this paper as [144]
In the citing paper
“For example, when normal-weight women tasted a sweetener with calories (sucrose), both the insula and dopaminergic midbrain areas became activated, whereas tasting a calorie-free sweetener (sucralose) only activated the insula (144).”
From Obesity and addiction: Neurobiological overlaps (2013) · cites this paper as [144]
In the citing paper
“For example, when normal weight women tasted a sweetener with calories (sucrose), both the insula and DA midbrain areas became activated, whereas tasting a calorie-free sweetener (sucralose) only activated the insula (103).”
From The Addictive Dimensionality of Obesity (2013) · cites this paper as [103]
In the citing paper
“Indeed, in humans, tasting palatable foods activated the insula and midbrain areas (102,103).”
From The Addictive Dimensionality of Obesity (2013) · cites this paper as [103]
In the citing paper
“Human imaging studies have shown that tasting palatable foods activated the insula and midbrain areas (DelParigi et al 2005;Frank et al 2008).”
From Food and Drug Reward: Overlapping Circuits in Human Obesity and Addiction (2011) · cites this paper as Frank et al 2008
In the citing paper
“However, the DA signaling may also be necessary for sensing the calorie content of food.For example, when normal weight women tasted a sweetener with calories (sucrose), both the insula and dopaminergic midbrain areas became activated, whereas tasting a calorie-free sweetener (sucralose) only activated the insula (Frank et al 2008).”
From Food and Drug Reward: Overlapping Circuits in Human Obesity and Addiction (2011) · cites this paper as Frank et al 2008
Citations
Cites
AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages
Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913
Central nervous system control of food intake
Schwartz, M. W., Woods, S. C., Porte, D., Seeley, R. J., & Baskin, D. G. (2000) · Nature · doi:10.1038/35007534 · Cited by 6,451
Anterior Cingulate Cortex, Error Detection, and the Online Monitoring of Performance
Carter, C. S., Braver, T. S., Barch, D. M., Botvinick, M. M., Noll, D., & Cohen, J. D. (1998) · Science · doi:10.1126/science.280.5364.747 · Cited by 3,273
Getting formal with dopamine and reward
Schultz, W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00967-4 · Cited by 2,574
Linear Systems Analysis of Functional Magnetic Resonance Imaging in Human V1
Boynton, G., Engel, S., Glover, G., & Heeger, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04207.1996 · Cited by 2,522
Central nervous system control of food intake and body weight
Morton, G. J., Cummings, D. E., Baskin, D. G., Barsh, G. S., & Schwartz, M. W. (2006) · Nature · doi:10.1038/nature05026 · Cited by 2,503
Food reward: brain substrates of wanting and liking
Berridge, K. C. (1996) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00033-b · Cited by 1,901
The receptors and cells for mammalian taste
Chandrashekar, J. V., Hoon, M. A., Ryba, N. J. P., & Zuker, C. S. (2006) · Nature · doi:10.1038/nature05401 · Cited by 1,632
Temporal difference models and reward-related learning in the human brain
O'Doherty, J. P., Dayan, P., Friston, K., Critchley, H., & Dolan, R. J. (2003) · Neuron · doi:10.1016/s0896-6273(03)00169-7 · Cited by 1,522
Reward representations and reward-related learning in the human brain: Insights from neuroimaging
O’Doherty, J. P. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.10.016 · Cited by 1,426
Eating Disorder Inventory-2 ; Pro-fessional Manual
Garner, D. (1991) · Medical Entomology and Zoology · Cited by 1,276
Dissociation of Neural Representation of Intensity and Affective Valuation in Human Gustation
Small, D. M., Gregory, M. D., Mak, Y. E., Gitelman, D. R., Mesulam, M. M., & Parrish, T. B. (2003) · Neuron · doi:10.1016/s0896-6273(03)00467-7 · Cited by 812
Prediction of immediate and future rewards differentially recruits cortico-basal ganglia loops
Tanaka, S. C., Doya, K., Okada, G., Ueda, K., Okamoto, Y., & Yamawaki, S. (2004) · Nature Neuroscience · doi:10.1038/nn1279 · Cited by 779
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
Peciña, S., & Berridge, K. C. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2329-05.2005 · Cited by 671
Detection of Sweet and Umami Taste in the Absence of Taste Receptor T1r3
Damak, S., Rong, M., Yasumatsu, K., Kokrashvili, Z., Varadarajan, V., Zou, S., Jiang, P., Ninomiya, Y., & Margolskee, R. F. (2003) · Science · doi:10.1126/science.1087155 · Cited by 632
Forebrain emotional asymmetry: a neuroanatomical basis?
Craig, A. D. (. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.10.005 · Cited by 626
The orbital and medial prefrontal circuit through the primate basal ganglia
Haber, S., Kunishio, K., Mizobuchi, M., & Lynd-Balta, E. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-07-04851.1995 · Cited by 605
Menstrual cycle phase modulates reward-related neural function in women
Dreher, J.-C., Schmidt, P. J., Kohn, P., Furman, D., Rubinow, D., & Berman, K. F. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605569104 · Cited by 567
Representations of Pleasant and Painful Touch in the Human Orbitofrontal and Cingulate Cortices
Rolls, E. T. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.308 · Cited by 535
Sensory-specific satiety-related olfactory activation of the human orbitofrontal cortex
OʼDoherty, J., Rolls, E. T., Francis, S., Bowtell, R., McGlone, F., Kobal, G., Renner, B., & Ahne, G. (2000) · NeuroReport · doi:10.1097/00001756-200002070-00035 · Cited by 482
Sensory-specific satiety-related olfactory activation of the human orbitofrontal cortex
OʼDoherty, J., Rolls, E. T., Francis, S., Bowtell, R., McGlone, F., Kobal, G., Renner, B., & Ahne, G. (2000) · NeuroReport · doi:10.1097/00001756-200003200-00046 · Cited by 361
Finlayson, G., King, N. A., & Blundell, J. E. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.08.020 · Cited by 342
Chikama, M., Mcfarland, N. R., Amaral, D., & Haber, S. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-24-09686.1997 · Cited by 333
Distinct Contributions of T1R2 and T1R3 Taste Receptor Subunits to the Detection of Sweet Stimuli
Nie, Y., Vigues, S., Hobbs, J. R., Conn, G. L., & Munger, S. D. (2005) · Current Biology · doi:10.1016/j.cub.2005.09.037 · Cited by 323
The neural mechanisms of gustation: A distributed processing code
Simon, S. A., de Araujo, I. E., Gutierrez, R., & Nicolelis, M. A. L. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn2006 · Cited by 305
Projections of thalamic gustatory and lingual areas in the monkey, Macaca fascicularis
Pritchard, T. C., Hamilton, R. B., Morse, J. R., & Norgren, R. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902440208 · Cited by 292
Gustatory responses of single neurons in the insula of the macaque monkey
Yaxley, S., Rolls, E. T., & Sienkiewicz, Z. J. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.4.689 · Cited by 262
Wagner, A., Aizenstein, H., Mazurkewicz, L., Fudge, J., Frank, G. K., Putnam, K., Bailer, U. F., Fischer, L., & Kaye, W. H. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301443 · Cited by 261
Self-citationVentral pallidum firing codes hedonic reward: when a bad taste turns good
Tindell, A. J., Smith, K. S., Peciña, S., Berridge, K. C., & Aldridge, J. W. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00576.2006 · Cited by 241
Altering expectancy dampens neural response to aversive taste in primary taste cortex
Nitschke, J. B., Dixon, G. E., Sarinopoulos, I., Short, S. J., Cohen, J. D., Smith, E. E., Kosslyn, S. M., Rose, R. M., & Davidson, R. J. (2006) · Nature Neuroscience · doi:10.1038/nn1645 · Cited by 199
The Sweetness and Pleasantness of Sugars
MOSKOWITZ, H. R. (1971) · The American Journal of Psychology · doi:10.2307/1420470 · Cited by 195
Scott, T. R., & Plata‐Saláman, C. R. (1999) · Physiology & Behavior · doi:10.1016/s0031-9384(99)00115-8 · Cited by 186
Stinus, L., Koob, G. F., LING, N. C., Bloom, F. E., & Moal, M. L. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.4.2323 · Cited by 182
Veldhuizen, M., Bender, G., Constable, R. T., & Small, D. (2007) · Chemical Sensors · doi:10.1093/chemse/bjm025 · Cited by 179
Bitterness of sweeteners as a function of concentration
Schiffman, S. S., Booth, B. J., Losee, M. L., Pecore, S. D., & Warwick, Z. S. (1995) · Brain Research Bulletin · doi:10.1016/0361-9230(94)00225-p · Cited by 172
Insular and gustatory inputs to the caudal ventral striatum in primates
Fudge, J. L., Breitbart, M. A., Danish, M., & Pannoni, V. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20660 · Cited by 146
Self-citationGustatory cortex of primates: anatomy and physiology
Ogawa, H. (1994) · Neuroscience Research · doi:10.1016/0168-0102(94)90017-5 · Cited by 144
Neural Ensemble Coding of Satiety States
de Araújo, I. E., Gutiérrez, R., Oliveira-Maia, A. J., Pereira, A., Nicolelis, M. A. L., & Simon, S. A. (2006) · Neuron · doi:10.1016/j.neuron.2006.07.009 · Cited by 136
Emotion-Related Hemisphere Asymmetry: Subjective Emotional Responses to Laterally Presented Films
Wittling, W., & Roschmann, R. (1993) · Cortex · doi:10.1016/s0010-9452(13)80252-3 · Cited by 132
Metabolic sensing neurons and the control of energy homeostasis
Levin, B. E. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.07.003 · Cited by 126
Artificial sweetener use and one-year weight change among women
Stellman, S. D., & Garfinkel, L. (1986) · Preventive Medicine · doi:10.1016/0091-7435(86)90089-7 · Cited by 118
Effects of intense sweeteners on hunger, food intake, and body weight: a review
Rolls, B. (1991) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/53.4.872 · Cited by 112
Effects of sugar intake on body weight: a review
Vermunt, S. H. F., Pasman, W. J., Schaafsma, G., & Kardinaal, A. F. M. (2003) · Obesity Reviews · doi:10.1046/j.1467-789x.2003.00102.x · Cited by 97
Curtis, K., Davis, L. M., Johnson, A. L., Therrien, K., & Contreras, R. J. (2004) · Physiology and Behavior · doi:10.1016/j.physbeh.2003.11.007 · Cited by 90
Hedonic responses to taste solutions: a cross-cultural study of Japanese and Australians
Prescott, J., Laing, D. G., Bell, G., Yoshida, M., Gillmore, R., Allen, S., Yamazaki, K., & Ishii, R. (1992) · Chemical Senses · doi:10.1093/chemse/17.6.801 · Cited by 74
Gustatory processing: a dynamic systems approach
Jones, L. M., Fontanini, A., & Katz, D. B. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.06.011 · Cited by 72
Preferring one taste over another without recognizing either
Adolphs, R., Tranel, D., Koenigs, M. R., & Damásio, A. R. (2005) · Nature Neuroscience · doi:10.1038/nn1489 · Cited by 67
Sunday, S. R., Einhorn, A., & Ka, H. (1992) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/55.2.362 · Cited by 67
Frank, G., Kaye, W. H., Carter, C. S., Brooks, S., May, C. J., Fissell, K., & Stenger, V. A. (2003) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(03)00240-1 · Cited by 62
Self-citationEffects of satiety on self-stimulation of the orbitofrontal cortex in the rhesus monkey
Mora, F., AVRITH, D. B., Phillips, A. G., & Rolls, E. T. (1979) · Neuroscience Letters · doi:10.1016/0304-3940(79)90031-4 · Cited by 61
Brain Mechanisms of Sweetness and Palatability of Sugars
Yamamoto, T. (2003) · Nutrition Reviews · doi:10.1301/nr.2003.may.s5-s9 · Cited by 58
Stellman, S. D., & Garfinkel, L. (1988) · Appetite · doi:10.1016/s0195-6663(88)80051-5 · Cited by 45
Oral, post-oral and genetic interactions in sweet appetite
Sclafani, A. J. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.03.021 · Cited by 41
Richmond, B. J., Liu, Z., & Shidara, M. (2003) · Science · doi:10.1126/science.1087383 · Cited by 28
Altered Food Preference after Cortical Infarction: Korean Style
Kim, J. S., & Choi, S.-M. (2002) · Cerebrovascular Diseases · doi:10.1159/000047774 · Cited by 25
MOSKOWITZ, H. R. (2001) · Food Service Technology · doi:10.1046/j.1471-5740.2001.00011.x · Cited by 5
Select Methods of Food Analysis
Wiley, H. W. (1901) · Science · doi:10.1126/science.14.359.769 · Cited by 4
Connectional networks within the orbital and medial prefrontal cortex of macaque monkeys
Carmichael, S. T., & Price, J. L. (1996) · Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960722)371:2
Research works printed but not linked: 1
- FDA, 1998, Food additives permitted for direct addition to food for human consumption; sucralose, Fed. Regist., 63, 16417
Cited by
Sorted by citations
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657
Obesity and addiction: Neurobiological overlaps
Volkow, N. D., Wang, G. ‐., Tomasi, D., & Baler, R. D. (2013) · Obesity Reviews · doi:10.1111/j.1467-789x.2012.01031.x · Cited by 800
“Human imaging studies have shown that tasting palatable foods activated the insula and midbrain areas (143,144).”
BackgroundCraig, A. D. (. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0248-y · Cited by 600
Carbohydrate sensing in the human mouth: effects on exercise performance and brain activity
Chambers, E. S., Bridge, M., & Jones, D. A. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2008.164285 · Cited by 625
“This seems unlikely and it is notable that the only other non-nutritive sweetener, sucralose, that has been tested in this way showed patterns of activation that were distinct from those of a natural carbohydrate (Frank et al. 2008).”
BackgroundMethodResultFood and Drug Reward: Overlapping Circuits in Human Obesity and Addiction
Volkow, N. D., Wang, G. J., Fowler, J. S., Tomasi, D., & Baler, R. (2011) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2011_169 · Cited by 525
“Human imaging studies have shown that tasting palatable foods activated the insula and midbrain areas (DelParigi et al. 2005; Frank et al. 2008).”
Background
Metadata
- Authors
- Frank, G. K. W., Oberndorfer, T. A., Simmons, A. N., Paulus, M. P., Fudge, J. L., Yang, T. T., & Kaye, W. H.
- Affiliations
- Children's Hospital Colorado (US)
- University of California San Diego (US)
- University of Rochester Medicine (US)
- University of Pittsburgh (US)
- Corresponding author
- Kaye, Walter H.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2008-02
- Volume
- 39
- Issue
- 4
- Pages
- 1559-1569
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2083215956
- Cited by
- 274
- References
- 59
- Citations by year
- 2026: 12 · 2025: 18 · 2024: 10 · 2023: 10 · 2022: 15 · 2021: 23 · 2020: 20 · 2019: 15 · 2018: 20 · 2017: 23 · 2016: 20 · 2015: 10 · 2014: 20 · 2013: 22 · 2012: 7
- FWCI
- 6.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (UL1TR000005)
- National Center for Advancing Translational Sciences
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Biochemical Analysis and Sensing Techniques
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- sucrose, sucralose, artificial sweeteners, taste pleasantness, anterior insula, frontal operculum, striatum, anterior cingulate cortex, dopaminergic midbrain, functional connectivity, sugar substitution
- MeSH terms
- Adult, Afferent Pathways, Brain, Cerebral Cortex, Dopamine, Female, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Reward, Sucrose, Sweetening Agents, Taste, Taste Buds
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