The role of dopamine in visual imagery-An experimental pharmacological study.

BCAA aphantasia mental imagery priming tyrosine/phenylalanine-depletion

Journal

Journal of neuroscience research
ISSN: 1097-4547
Titre abrégé: J Neurosci Res
Pays: United States
ID NLM: 7600111

Informations de publication

Date de publication:
18 Oct 2023
Historique:
revised: 18 09 2023
received: 25 05 2023
accepted: 03 10 2023
medline: 18 10 2023
pubmed: 18 10 2023
entrez: 18 10 2023
Statut: aheadofprint

Résumé

Mental imagery enables people to simulate experiences in their minds without the presence of an external stimulus. The underlying biochemical mechanisms are poorly understood but there is vague evidence that dopamine may play a significant role. A better understanding at the biochemical level could help to unravel the mechanisms of mental imagery and related phenomena such as aphantasia (= lack of voluntary mental imagery), but also opens up possibilities for interventions to enhance or restore mental imagery. To test the hypothesis that acute dopamine depletion leads to a decrease in the strength of mental imagery, N = 22 male participants will be administered an amino acid mixture containing branched-chain amino acids (BCAAs) and tryptophan (TRP) to transiently reduce dopamine synthesis and further N = 22 male participants will receive a placebo. Plasma prolactin (PRL) levels are determined as a peripheral marker of brain dopamine function. The strength of mental imagery will be measured before and after ingestion of the BCAA/TRP mixture using the method of mental imagery priming. Additional exploratory analyses will use genetic data to investigate possible effects of variations on dopaminergic gene loci (e.g., DAT1) on dopamine levels and strength of mental imagery. The results show […].

Identifiants

pubmed: 37849328
doi: 10.1002/jnr.25262
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 The Authors. Journal of Neuroscience Research published by Wiley Periodicals LLC.

Références

Ball, P., Knuppen, R., Haupt, M., & Breuer, H. (1972). Interactions between estrogens and catechol amines. 3. Studies on the methylation of catechol estrogens, catechol amines and other catechols by the ctechol-O-methyltransferases of human liver. Journal of Clinical Endocrinology and Metabolism, 34(4), 736-746. https://doi.org/10.1210/jcem-34-4-736
Bazzett, T. J., & Becker, J. B. (1994). Sex differences in the rapid and acute effects of estrogen on striatal D2 dopamine receptor binding. Brain Research, 637(1-2), 163-172. https://doi.org/10.1016/0006-8993(94)91229-7
Beck, A. T., Steer, R. A., & Brown, G. (1996). Beck Depression Inventory-II. San Antonio, 78, 490-498.
Bischof, M., & Bassetti, C. L. (2004). Total dream loss: A distinct neuropsychological dysfunction after bilateral PCA stroke. Annals of Neurology, 56(4), 583-586. https://doi.org/10.1002/ana.20246
Blumberg, M. S., Lesku, J. A., Libourel, P.-A., Schmidt, M. H., & Rattenborg, N. C. (2020). What is REM sleep? Current Biology, 30(1), R38-R49. https://doi.org/10.1016/j.cub.2019.11.045
Breyer, B., & Bluemke, M. (2016). Deutsche version der positive and negative affect schedule PANAS (GESIS panel). ZIS-GESIS Leibniz Institute for the Social Sciences. https://www.researchgate.net/publication/309210530_Deutsche_Version_der_Positive_and_Negative_Affect_Schedule_PANAS_GESIS_Panel, https://doi.org/10.6102/zis242
Colzato, L. S., & Hommel, B. (2014). Effects of estrogen on higher-order cognitive functions in unstressed human females may depend on individual variation in dopamine baseline levels. Frontiers in Neuroscience, 8, 65. https://doi.org/10.3389/fnins.2014.00065
Dance, C. J., Ipser, A., & Simner, J. (2022). The prevalence of aphantasia (imagery weakness) in the general population. Consciousness and Cognition, 97, 103243. https://doi.org/10.1016/j.concog.2021.103243
Dance, C. J., Jaquiery, M., Eagleman, D. M., Porteous, D., Zeman, A., & Simner, J. (2021). What is the relationship between Aphantasia, Synaesthesia and Autism? Consciousness and Cognition, 89, 103087. https://doi.org/10.1016/j.concog.2021.103087
David, D., de Faria, L., Lapeyra, O., & Mellman, T. A. (2004). Adjunctive risperidone treatment in combat veterans with chronic PTSD. Journal of Clinical Psychopharmacology, 24(5), 556-559. https://doi.org/10.1097/01.jcp.0000138771.46353.59
Dawes, A. J., Keogh, R., Andrillon, T., & Pearson, J. (2020). A cognitive profile of multi-sensory imagery, memory and dreaming in aphantasia. Scientific Reports, 10(1), 10022. https://doi.org/10.1038/s41598-020-65705-7
Dawes, A. J., Keogh, R., Robuck, S., & Pearson, J. (2022). Memories with a blind mind: Remembering the past and imagining the future with aphantasia. Cognition, 227, 105192. https://doi.org/10.1016/j.cognition.2022.105192
De Gregorio, D., Comai, S., Posa, L., & Gobbi, G. (2016). d-lysergic acid diethylamide (LSD) as a model of psychosis: Mechanism of action and pharmacology. International Journal of Molecular Sciences, 17(11), 1953. https://doi.org/10.3390/ijms17111953
Diederich, N. J., Fénelon, G., Stebbins, G., & Goetz, C. G. (2009). Hallucinations in Parkinson disease. Nature Reviews Neurology, 5(6), 331-342. https://doi.org/10.1038/nrneurol.2009.62
Dubol, M., Epperson, C. N., Sacher, J., Pletzer, B., Derntl, B., Lanzenberger, R., Sundström-Poromaa, I., & Comasco, E. (2021). Neuroimaging the menstrual cycle: A multimodal systematic review. Frontiers in Neuroendocrinology, 60, 100878. https://doi.org/10.1016/j.yfrne.2020.100878
Fazekas, P., Nanay, B., & Pearson, J. (2021). Offline perception: An introduction. Philosophical Transactions of the Royal Society B: Biological Sciences, 376(1817), 20190686. https://doi.org/10.1098/rstb.2019.0686
Fernstrom, J. D. (2005). Branched-chain amino acids and brain function. Journal of Nutrition, 135(Suppl. 6), 1539S-1546S. https://doi.org/10.1093/jn/135.6.1539S
Fernstrom, J. D. (2013). Large neutral amino acids: Dietary effects on brain neurochemistry and function. Amino Acids, 45(3), 419-430. https://doi.org/10.1007/s00726-012-1330-y
Fernstrom, J. D., & Fernstrom, M. H. (2007). Tyrosine, phenylalanine, and catecholamine synthesis and function in the brain. Journal of Nutrition, 137(Suppl. 1), 1539S-1547S; discussion 1548S. https://doi.org/10.1093/jn/137.6.1539S
Fitzgerald, P., & Dinan, T. G. (2008). Prolactin and dopamine: What is the connection? A review article. Journal of Psychopharmacology, 22(Suppl. 2), 12-19. https://doi.org/10.1177/0269216307087148
Fulford, J., Milton, F., Salas, D., Smith, A., Simler, A., Winlove, C., & Zeman, A. (2018). The neural correlates of visual imagery vividness-An fMRI study and literature review. Cortex, 105, 26-40. https://doi.org/10.1016/j.cortex.2017.09.014
Gadow, K. D., Roohi, J., DeVincent, C. J., & Hatchwell, E. (2008). Association of ADHD, tics, and anxiety with dopamine transporter (DAT1) genotype in autism spectrum disorder. Journal of Child Psychology and Psychiatry, and Allied Disciplines, 49(12), 1331-1338. https://doi.org/10.1111/j.1469-7610.2008.01952.x
Gaillard, J. M., & Moneme, A. (1977). Modification of dream content after preferential blockade of mesolimbic and mesocortical dopaminergic systems. Journal of Psychiatric Research, 13(4), 247-256. https://doi.org/10.1016/S0022-3956(77)90020-6
Gijsman, H. J., Scarnà, A., Harmer, C. J., McTavish, S. B., Odontiadis, J., Cowen, P. J., & Goodwin, G. M. (2002). A dose-finding study on the effects of branch chain amino acids on surrogate markers of brain dopamine function. Psychopharmacology, 160(2), 192-197. https://doi.org/10.1007/s00213-001-0970-5
Gottesmann, C. (2002). The neurochemistry of waking and sleeping mental activity: The disinhibition-dopamine hypothesis. Psychiatry and Clinical Neurosciences, 56(4), 345-354. https://doi.org/10.1046/j.1440-1819.2002.01022.x
Greenberg, D. L., & Knowlton, B. J. (2014). The role of visual imagery in autobiographical memory. Memory & Cognition, 42(6), 922-934. https://doi.org/10.3758/s13421-014-0402-5
Gulyás, E., Gombos, F., Sütöri, S., Lovas, A., Ziman, G., & Kovács, I. (2022). Visual imagery vividness declines across the lifespan. Cortex, 154, 365-374. https://doi.org/10.1016/j.cortex.2022.06.011
Halberstadt, A. L., & Geyer, M. A. (2011). Multiple receptors contribute to the behavioral effects of indoleamine hallucinogens. Neuropharmacology, 61(3), 364-381. https://doi.org/10.1016/j.neuropharm.2011.01.017
Harmer, C. J., McTavish, S. F., Clark, L., Goodwin, G. M., & Cowen, P. J. (2001). Tyrosine depletion attenuates dopamine function in healthy volunteers. Psychopharmacology, 154(1), 105-111. https://doi.org/10.1007/s002130000613
Harrison, P. J., & Tunbridge, E. M. (2008). Catechol-O-methyltransferase (COMT): A gene contributing to sex differences in brain function, and to sexual dimorphism in the predisposition to psychiatric disorders. Neuropsychopharmacology, 33(13), 3037-3045. https://doi.org/10.1038/sj.npp.1301543
Holmes, E. A., & Mathews, A. (2010). Mental imagery in emotion and emotional disorders. Clinical Psychology Review, 30(3), 349-362. https://doi.org/10.1016/j.cpr.2010.01.001
Holzinger, B., & Mayer, L. (2020). Lucid dreaming brain network based on Tholey's 7 Klartraum criteria. Frontiers in Psychology, 11, 1885. https://doi.org/10.3389/fpsyg.2020.01885
Howes, O. D., & Kapur, S. (2009). The dopamine hypothesis of schizophrenia: Version III-The final common pathway. Schizophrenia Bulletin, 35(3), 549-562. https://doi.org/10.1093/schbul/sbp006
Iddi, S., & Donohue, M. C. (2022). Power and sample size for longitudinal models in R-the longpower package and shiny app. R Journal, 14(1), 264-281.
Jacobs, E., & D'Esposito, M. (2011). Estrogen shapes dopamine-dependent cognitive processes: Implications for women's health. Journal of Neuroscience, 31(14), 5286-5293. https://doi.org/10.1523/JNEUROSCI.6394-10.2011
Ji, J. L., Kavanagh, D. J., Holmes, E. A., MacLeod, C., & Di Simplicio, M. (2019). Mental imagery in psychiatry: Conceptual & clinical implications. CNS Spectrums, 24(1), 114-126. https://doi.org/10.1017/S1092852918001487
Jungmann, S. M., Becker, F., & Witthöft, M. (2022). Erfassung der Lebendigkeit mentaler Vorstellungsbilder. Diagnostica, 68(3), 125-136. https://doi.org/10.1026/0012-1924/a000291
Kay, L., Keogh, R., Andrillon, T., & Pearson, J. (2022). The pupillary light response as a physiological index of aphantasia, sensory and phenomenological imagery strength. eLife, 11, e72484. https://doi.org/10.7554/eLife.72484
Keogh, R., Bergmann, J., & Pearson, J. (2020). Cortical excitability controls the strength of mental imagery. eLife, 9, e50232. https://doi.org/10.7554/eLife.50232
Keogh, R., & Pearson, J. (2018). The blind mind: No sensory visual imagery in aphantasia. Cortex, 105, 53-60. https://doi.org/10.1016/j.cortex.2017.10.012
Keogh, R., Wicken, M., & Pearson, J. (2023). Fewer intrusive memories in aphantasia: Using the trauma film paradigm as a laboratory model of PTSD. Vorab-Onlinepublikation. https://doi.org/10.31234/osf.io/7zqfe
Kjaer, T. W., Bertelsen, C., Piccini, P., Brooks, D., Alving, J., & Lou, H. C. (2002). Increased dopamine tone during meditation-induced change of consciousness. Cognitive Brain Research, 13(2), 255-259. https://doi.org/10.1016/S0926-6410(01)00106-9
Königsmark, V. T., Bergmann, J., & Reeder, R. R. (2021). The Ganzflicker experience: High probability of seeing vivid and complex pseudo-hallucinations with imagery but not aphantasia. Cortex, 141, 522-534. https://doi.org/10.1016/j.cortex.2021.05.007
Kraehenmann, R., Pokorny, D., Vollenweider, L., Preller, K. H., Pokorny, T., Seifritz, E., & Vollenweider, F. X. (2017). Dreamlike effects of LSD on waking imagery in humans depend on serotonin 2A receptor activation. Psychopharmacology, 234(13), 2031-2046. https://doi.org/10.1007/s00213-017-4610-0
Lambert, M. T. (2006). Aripiprazole in the management of post-traumatic stress disorder symptoms in returning global war on terrorism veterans. International Clinical Psychopharmacology, 21(3), 185-187. https://doi.org/10.1097/01.yic.0000185021.48279.00
Leucht, S., Heres, S., Kissling, W., & Davis, J. M. (2011). Evidence-based pharmacotherapy of schizophrenia. International Journal of Neuropsychopharmacology, 14(2), 269-284. https://doi.org/10.1017/S1461145710001380
Leyton, M., Dagher, A., Boileau, I., Casey, K., Baker, G. B., Diksic, M., Gunn, R., Young, S. N., & Benkelfat, C. (2004). Decreasing amphetamine-induced dopamine release by acute phenylalanine/tyrosine depletion: A PET/[11C]raclopride study in healthy men. Neuropsychopharmacology, 29(2), 427-432. https://doi.org/10.1038/sj.npp.1300328
Leyton, M., Young, S. N., Pihl, R. O., Etezadi, S., Lauze, C., Blier, P., Baker, G. B., & Benkelfat, C. (2000). Effects on mood of acute phenylalanine/tyrosine depletion in healthy women. Neuropsychopharmacology, 22(1), 52-63. https://doi.org/10.1016/S0893-133X(99)00086-X
Li, S.-C., Lindenberger, U., & Bäckman, L. (2010). Dopaminergic modulation of cognition across the life span. Neuroscience and Biobehavioral Reviews, 34(5), 625-630. https://doi.org/10.1016/j.neubiorev.2010.02.003
Marchesini, G., Bianchi, G. P., Vilstrup, H., Checchia, G. A., Patrono, D., & Zoli, M. (1987). Plasma clearances of branched-chain amino acids in control subjects and in patients with cirrhosis. Journal of Hepatology, 4(1), 108-117. https://doi.org/10.1016/s0168-8278(87)80017-x
Marks, D. F. (1973). Visual imagery differences in the recall of pictures. British Journal of Psychology, 64(1), 17-24. https://doi.org/10.1111/j.2044-8295.1973.tb01322.x
McKelvie, S. J. (1995). The VVIQ as a psychometric test of individual differences in visual imagery vividness: A critical quantitative review and plea for direction. Journal of Mental Imagery, 19(3-4), 1-106.
McTavish, S. F., Callado, L., Cowen, P. J., & Sharp, T. (1999). Comparison of the effects of alpha-methyl-p-tyrosine and a tyrosine-free amino acid load on extracellular noradrenaline in the rat hippocampus in vivo. Journal of Psychopharmacology, 13(4), 379-384. https://doi.org/10.1177/026988119901300408
Milton, F., Fulford, J., Dance, C., Gaddum, J., Heuerman-Williamson, B., Jones, K., Knight, K. F., MacKisack, M., Winlove, C., & Zeman, A. (2021). Behavioral and neural signatures of visual imagery vividness extremes: Aphantasia versus hyperphantasia. Cerebral Cortex Communications, 2(2), tgab035. https://doi.org/10.1093/texcom/tgab035
Mitchell, J. M., Weinstein, D., Vega, T., & Kayser, A. S. (2018). Dopamine, time perception, and future time perspective. Psychopharmacology, 235(10), 2783-2793. https://doi.org/10.1007/s00213-018-4971-z
Montgomery, A. J., McTavish, S. F. B., Cowen, P. J., & Grasby, P. M. (2003). Reduction of brain dopamine concentration with dietary tyrosine plus phenylalanine depletion: An [11C]raclopride PET study. American Journal of Psychiatry, 160(10), 1887-1889. https://doi.org/10.1176/appi.ajp.160.10.1887
Monzel, M., Keidel, K., & Reuter, M. (2021). Imagine, and you will find-Lack of attentional guidance through visual imagery in aphantasics. Attention, Perception, & Psychophysics, 83(6), 2486-2497. https://doi.org/10.3758/s13414-021-02307-z
Monzel, M., Mitchell, D., Macpherson, F., Pearson, J., & Zeman, A. (2022a). Aphantasia, dysikonesia, anauralia: Call for a single term for the lack of mental imagery-commentary on Dance et al. (2021) and Hinwar and Lambert (2021). Cortex, 150, 149-152. https://doi.org/10.1016/j.cortex.2022.02.002
Monzel, M., Mitchell, D., Macpherson, F., Pearson, J., & Zeman, A. (2022b). Proposal for a consistent definition of aphantasia and hyperphantasia: A response to Lambert and Sibley (2022) and Simner and Dance (2022). Cortex, 152, 74-76. https://doi.org/10.1016/j.cortex.2022.04.003
Monzel, M., & Reuter, M. (2023). Where's Wanda? The influence of visual imagery vividness on visual search speed measured by means of hidden object pictures. Attention, Perception, & Psychophysics, Vorab-Onlinepublikation. https://doi.org/10.3758/s13414-022-02645-6
Monzel, M., Vetterlein, A., Hogeterp, S., & Reuter, M. (in press). No increased prevalence of prosopagnosia in aphantasia: Visual recognition deficits are small and not restricted to faces. Perception.
Monzel, M., Vetterlein, A., & Reuter, M. (2022c). Memory deficits in aphantasics are not restricted to autobiographical memory-Perspectives from the dual coding approach. Journal of Neuropsychology, 16(2), 444-461. https://doi.org/10.1111/jnp.12265
Monzel, M., Vetterlein, A., & Reuter, M. (2022d). No general pathological significance of aphantasia: An evaluation based on criteria for mental disorders. Scandinavian Journal of Psychology, Vorab-Onlinepublikation. https://doi.org/10.1111/sjop.12887
Nanay, B. (2018). Multimodal mental imagery. Cortex, 105, 125-134. https://doi.org/10.1016/j.cortex.2017.07.006
Nanay, B. (2023). Mental imagery: Philosophy, psychology, neuroscience. Oxford University Press Incorporated. https://ebookcentral.proquest.com/lib/kxp/detail.action?docID=7219894
Neuhaus, A. H., Goldberg, T. E., Hassoun, Y., Bates, J. A., Nassauer, K. W., Sevy, S., Opgen-Rhein, C., & Malhotra, A. K. (2009). Acute dopamine depletion with branched chain amino acids decreases auditory top-down event-related potentials in healthy subjects. Schizophrenia Research, 111(1-3), 167-173. https://doi.org/10.1016/j.schres.2009.03.023
Nir, Y., & Tononi, G. (2010). Dreaming and the brain: From phenomenology to neurophysiology. Trends in Cognitive Sciences, 14(2), 88-100. https://doi.org/10.1016/j.tics.2009.12.001
O'Donnell, C., Di Simplicio, M., Brown, R., Holmes, E. A., & Burnett Heyes, S. (2018). The role of mental imagery in mood amplification: An investigation across subclinical features of bipolar disorders. Cortex, 105, 104-117. https://doi.org/10.1016/j.cortex.2017.08.010
Pagel, J. F., & Helfter, P. (2003). Drug induced nightmares-An etiology based review. Human Psychopharmacology, 18(1), 59-67. https://doi.org/10.1002/hup.465
Pearson, J. (2014). New directions in mental-imagery research: The binocular-rivalry technique and decoding fMRI patterns. Current Directions in Psychological Science, 23(3), 178-183. https://doi.org/10.1177/0963721414532287
Pearson, J., Clifford, C. W. G., & Tong, F. (2008). The functional impact of mental imagery on conscious perception. Current Biology, 18(13), 982-986. https://doi.org/10.1016/j.cub.2008.05.048
Pearson, J., Naselaris, T., Holmes, E. A., & Kosslyn, S. M. (2015). Mental imagery: Functional mechanisms and clinical applications. Trends in Cognitive Sciences, 19(10), 590-602. https://doi.org/10.1016/j.tics.2015.08.003
Pearson, J., Rademaker, R. L., & Tong, F. (2011). Evaluating the mind's eye: The metacognition of visual imagery. Psychological Science, 22(12), 1535-1542. https://doi.org/10.1177/0956797611417134
Rabey, J. M., Vardi, J., Askenazi, J. J., & Streifler, M. (1977). l-tryptophan administration in l-dopa-induced hallucinations in elderly parkinsonian patients. Gerontology, 23(6), 438-444. https://doi.org/10.1159/000212220
Roelfsema, F., Pijl, H., Keenan, D. M., & Veldhuis, J. D. (2012). Prolactin secretion in healthy adults is determined by gender, age and body mass index. PLoS ONE, 7(2), e31305. https://doi.org/10.1371/journal.pone.0031305
Sanna, L. J. (2000). Mental simulation, affect, and personality. Current Directions in Psychological Science, 9(5), 168-173. https://doi.org/10.1111/1467-8721.00086
Scarnà, A., Gijsman, H. J., Harmer, C. J., Goodwin, G. M., & Cowen, P. J. (2002). Effect of branch chain amino acids supplemented with tryptophan on tyrosine availability and plasma prolactin. Psychopharmacology, 159(2), 222-223. https://doi.org/10.1007/s00213-001-0963-4
Scarnà, A., McTavish, S. F. B., Cowen, P. J., Goodwin, G. M., & Rogers, R. D. (2005). The effects of a branched chain amino acid mixture supplemented with tryptophan on biochemical indices of neurotransmitter function and decision-making. Psychopharmacology, 179(4), 761-768. https://doi.org/10.1007/s00213-004-2105-2
Schmack, K., Bosc, M., Ott, T., Sturgill, J. F., & Kepecs, A. (2021). Striatal dopamine mediates hallucination-like perception in mice. Science, 372(6537), eabf4740. https://doi.org/10.1126/science.abf4740
Sevy, S., Hassoun, Y., Bechara, A., Yechiam, E., Napolitano, B., Burdick, K., Delman, H., & Malhotra, A. (2006). Emotion-based decision-making in healthy subjects: Short-term effects of reducing dopamine levels. Psychopharmacology, 188(2), 228-235. https://doi.org/10.1007/s00213-006-0450-z
Shadish, W. R., Cook, T. D., & Campbell, D. T. (2002). Experimental and quasi-experimental designs for generalized causal inference. Houghton Mifflin. https://iaes.cgiar.org/sites/default/files/pdf/147.pdf
Shang, C.-Y., Lin, H.-Y., & Gau, S. S.-F. (2021). Effects of the dopamine transporter gene on striatal functional connectivity in youths with attention-deficit/hyperactivity disorder. Psychological Medicine, 51(5), 835-845. https://doi.org/10.1017/S0033291719003830
Shang, C.-Y., Lin, H. Y., Tseng, W. Y., & Gau, S. S.-F. (2018). A haplotype of the dopamine transporter gene modulates regional homogeneity, gray matter volume, and visual memory in children with attention-deficit/hyperactivity disorder. Psychological Medicine, 48(15), 2530-2540. https://doi.org/10.1017/S0033291718000144
Solms, M. (2000). Dreaming and REM sleep are controlled by different brain mechanisms. Behavioral and Brain Sciences, 23(6), 843-850; discussion 904-1121. https://doi.org/10.1017/s0140525x00003988
Ten Eycke, K. D., & Müller, U. (2015). Brief report: New evidence for a social-specific imagination deficit in children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 45(1), 213-220. https://doi.org/10.1007/s10803-014-2206-7
Thompson, D. F., & Pierce, D. R. (1999). Drug-induced nightmares. Annals of Pharmacotherapy, 33(1), 93-98. https://doi.org/10.1345/aph.18150
Weil, R. S., & Reeves, S. (2020). Hallucinations in Parkinson's disease: New insights into mechanisms and treatments. Advances in Clinical Neuroscience & Rehabilitation, 19(4), 20-22. https://doi.org/10.47795/ONNS5189
Zeman, A., Dewar, M., & Della Sala, S. (2015). Lives without imagery-Congenital aphantasia. Cortex, 73, 378-380. https://doi.org/10.1016/j.cortex.2015.05.019
Zeman, A., Milton, F., Della Sala, S., Dewar, M., Frayling, T., Gaddum, J., Hattersley, A., Heuerman-Williamson, B., Jones, K., MacKisack, M., & Winlove, C. (2020). Phantasia-the psychological significance of lifelong visual imagery vividness extremes. Cortex, 130, 426-440. https://doi.org/10.1016/j.cortex.2020.04.003
Zürcher, N. R., Walsh, E. C., Phillips, R. D., Cernasov, P. M., Tseng, C.-E. J., Dharanikota, A., Smith, E., Li, Z., Kinard, J. L., Bizzell, J. C., Greene, R. K., Dillon, D., Pizzagalli, D. A., Izquierdo-Garcia, D., Truong, K., Lalush, D., Hooker, J. M., & Dichter, G. S. (2021). A simultaneous [11C]raclopride positron emission tomography and functional magnetic resonance imaging investigation of striatal dopamine binding in autism. Translational Psychiatry, 11(1), 33. https://doi.org/10.1038/s41398-020-01170-0

Auteurs

Merlin Monzel (M)

Department of Psychology, University of Bonn, Bonn, Germany.

Jana Karneboge (J)

Department of Psychology, University of Bonn, Bonn, Germany.

Martin Reuter (M)

Department of Psychology, University of Bonn, Bonn, Germany.
Center for Economics and Neuroscience (CENs), Laboratory of Neurogenetics, University of Bonn, Bonn, Germany.

Classifications MeSH