Abstract
Transcranial direct current stimulation (tDCS) has been widely used for modulating sensory, motor and cognitive functions, but there are only few attempts to induce and change illusory perception. Visual illusions have been the most traditional and effective way to investigate visual processing through the comparison between physical reality and subjective reports. Here we used tDCS to modulate two different visual illusions, namely the Brentano illusion and the glare effect, with the aim of uncovering the influence of top-down mechanisms on bottom-up visual perception in two experiments. In Experiment 1, to a first group of subjects, real and sham cathodal tDCS (2 mA, 10 min) were applied over the left and right posterior parietal cortices (PPC). In Experiment 2, real and sham cathodal tDCS were applied to the left and right occipital cortices (OC) to a second group of participants. Results showed that tDCS was effective in modulating only the Brentano illusion, but not the glare effect. tDCS increased the Brentano illusion but specifically for the stimulated cortical area (right PPC), illusion direction (leftward), visual hemispace (left), and illusion length (160 mm). These findings suggest the existence of an inhibitory modulation of top-down mechanisms on bottom-up visual processing specifically for the Brentano illusion, but not for the glare effect. The lack of effect of occipital tDCS should consider the possible role of ocular compensation or of the unstimulated hemisphere, which deserves further investigations.
Similar content being viewed by others
References
Antal A, Kincses TZ, Nitsche MA, Bartfai O, Paulus W (2004) Excitability changes induced in the human primary visual cortex by transcranial direct current stimulation: direct electrophysiological evidence. Invest Ophthalmol Vis Sci 45(2):702–707
Boggio PS, Zaghi S, Fregni F (2009) Modulation of emotions associated with images of human pain using anodal transcranial direct current stimulation (tDCS). Neuropsychologia 47(1):212–217
Bolognini N, Rossetti A, Casati C, Mancini F, Vallar G (2011) Neuromodulation of multisensory perception: a tDCS study of the sound-induced flash illusion. Neuropsychologia 49(2):231–237
Boyaci H, Fang F, Murray SO, Kersten D (2007) Responses to lightness variations in early human visual cortex. Curr Biol 17(11):989–993
Cabral-Calderin Y, Schmidt-Samoa C, Wilke M (2015) Rhythmic gamma stimulation affects bistable perception. J Cognit Neurosci 27(7):1298–1307
Convento S, Romano D, Maravita A, Bolognini N (2018) Roles of the right temporo-parietal and premotor cortices in self-location and body ownership. Eur J Neurosci 47(11):1289–1302
Core Team R (2017) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna
Coren S, Girgus JS (1978) Seeing is deceiving: the psychology of visual illusions. Lawrence Erlbaum, Oxford
Daini R, Angelelli P, Antonucci G, Cappa SF, Vallar G (2002) Exploring the syndrome of spatial unilateral neglect through an illusion of length. Exp Brain Res 144(2):224–237
Facchin A, Daini R, Zavagno D (2017) The glare effect test and the impact of age on luminosity thresholds. Front Psychol 8:1132
Facchin A, Vallar G, Daini R (submitted) The Brentano Illusion Test (BRIT): an implicit task of perceptual processing for the assessment of visual field defects in neglect patients. Neuropsychol Rehabil
Ffytche DH, Zeki S (1996) Brain activity related to the perception of illusory contours. Neuroimage 3(1):S272–S272
Gandiga PC, Hummel FC, Cohen LG (2006) Transcranial DC stimulation (tDCS): a tool for double-blind sham-controlled clinical studies in brain stimulation. Clin Neurophysiol 117(4):845–850
Giglia G, Mattaliano P, Puma A, Rizzo S, Fierro B, Brighina F (2011) Neglect-like effects induced by tDCS modulation of posterior parietal cortices in healthy subjects. Brain Stimul 4(4):294–299
Golay L, Schnider A, Ptak R (2008) Cortical and subcortical anatomy of chronic spatial neglect following vascular damage. Behav Brain Funct 4(1):43
Haynes JD, Lotto RB, Rees G (2004) Responses of human visual cortex to uniform surfaces. Proc Natl Acad Sci 101(12):4286–4291
Healton EB, Navarro C, Bressman S, Brust JC (1982) Subcortical neglect. Neurology 32(7):776
Heilman KM, Valenstein E (1979) Mechanisms underlying hemispatial neglect. Ann Neurol 5(2):166–170
Hirsch J, DeLaPaz RL, Relkin NR, Victor J, Kim K, Li T, Borden P, Rubin N, Shapley R (1995) Illusory contours activate specific regions in human visual cortex: evidence from functional magnetic resonance imaging. Proc Natl Acad Sci 92(14):6469–6473
Hosmer DW Jr, Lemeshow S, Sturdivant RX (2013) Applied logistic regression, vol 398. Wiley, Hoboken
Husain M, Shapiro K, Martin J, Kennard C (1997) Abnormal temporal dynamics of visual attention in spatial neglect patients. Nature 385(6612):154
Ishiai S, Furukawa T, Tsukagoshi H (1987) Eye-fixation patterns in homonymous hemianopia and unilateral spatial neglect. Neuropsychologia 25(4):675–679
Karnath HO, Ferber S, Himmelbach M (2001) Spatial awareness is a function of the temporal not the posterior parietal lobe. Nature 411(6840):950–953
Karnath HO, Himmelbach M, Rorden C (2002) The subcortical anatomy of human spatial neglect: putamen, caudate nucleus and pulvinar. Brain 125(2):350–360
Karnath HO, Fruhmann Berger M, Küker W, Rorden C (2004) The anatomy of spatial neglect based on voxelwise statistical analysis: a study of 140 patients. Cereb Cortex 14(10):1164–1172
Kerkhoff G, Schenk T (2011) Line bisection in homonymous visual field defects—recent findings and future directions. Cortex 47(1):53–58
Larsson J, Amunts K, Gulyás B, Malikovic A, Zilles K, Roland PE (1999) Neuronal correlates of real and illusory contour perception: functional anatomy with PET. Eur J Neurosci 11(11):4024–4036
Leonards U, Troscianko T, Lazeyras F, Ibanez V (2005) Cortical distinction between the neural encoding of objects that appear to glow and those that do not. Cognit Brain Res 24(1):173–176
Lu H, Zavagno D, Liu Z (2006) The glare effect does not give rise to a longer-lasting afterimage. Perception 35(5):701–707
MacEvoy SP, Paradiso MA (2001) Lightness constancy in primary visual cortex. Proc Natl Acad Sci 98(15):8827–8831
Machner B, Sprenger A, Sander T, Heide W, Kimmig H, Helmchen C, Kömpf D (2009) Visual search disorders in acute and chronic homonymous hemianopia. Ann NY Acad Sci 1164:419–426
Marques LM, Lapenta OM, Merabet LB, Bolognini N, Boggio PS (2014) Tuning and disrupting the brain—modulating the McGurk illusion with electrical stimulation. Front Hum Neurosci 8:533
Mattingley JB, Bradshaw JL, Bradshaw JA (1995) The effects of unilateral visuospatial neglect on perception of Müller-Lyer illusory figures. Perception 24(4):415–433
Mendola JD, Dale AM, Fischl B, Liu AK, Tootell RB (1999) The representation of illusory and real contours in human cortical visual areas revealed by functional magnetic resonance imaging. J Neurosci 19(19):8560–8572
Nitsche MA, Paulus W (2001) Sustained excitability elevations induced by transcranial DC motor cortex stimulation in humans. Neurology 57(10):1899–1901
Nitsche MA, Liebetanz D, Antal A, Lang N, Tergau F, Paulus W (2003) Modulation of cortical excitability by weak direct current stimulation–technical, safety and functional aspects. Suppl Clin Neurophysiol 56:255–276
Nitsche MA, Cohen LG, Wassermann EM, Priori A, Lang N, Antal A, Paulus W, Hummel F, Boggio PS, Fregni F, Pascual-Leone A (2008) Transcranial direct current stimulation: state of the art 2008. Brain Stimul 1(3):206–223
Oldfield RC (1971) The assessment and analysis of handedness: the Edinburgh inventory. Neuropsychologia 9(1):97–113
Restle F, Decker J (1977) Size of the Mueller-Lyer illusion as a function of its dimensions: theory and data. Percept Psychophys 21(6):489–503
Rossi AF, Paradiso MA (1999) Neural correlates of perceived brightness in the retina, lateral geniculate nucleus, and striate cortex. J Neurosci 19(14):6145–6156
Rossi AF, Rittenhouse CD, Paradiso MA (1996) The representation of brightness in primary visual cortex. Science 273(5278):1104–1107
Rossi S, Hallett M, Rossini PM, Pascual-Leone A, The Safety of TMS Consensus Group (2009) Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research. Clin Neurophysiol 120(12):2008–2039
Rossini PM, Burke D, Chen R, Cohen LG, Daskalakis Z, Di Iorio R et al (2015) Non-invasive electrical and magnetic stimulation of the brain, spinal cord, roots and peripheral nerves: basic principles and procedures for routine clinical and research application. An updated report from an IFCN Committee. Clin Neurophysiol 126(6):1071–1107
Scocchia L, Bolognini N, Convento S, Stucchi N (2015) Cathodal transcranial direct current stimulation can stabilize perception of movement: evidence from the two-thirds power law illusion. Neurosci Lett 609:87–91
Strüber D, Rach S, Trautmann-Lengsfeld SA, Engel AK, Herrmann CS (2014) Antiphasic 40 Hz oscillatory current stimulation affects bistable motion perception. Brain Topogr 27(1):158–171
Vallar G (1998) Spatial hemineglect in humans. Trends in Cognit Sci 2(3):87–97
Vallar G (2001) Extrapersonal visual unilateral spatial neglect and its neuroanatomy. Neuroimage 14(1):S52–S58
Vallar G, Bolognini N (2011) Behavioural facilitation following brain stimulation: implications for neurorehabilitation. Neuropsychol Rehabil 21(5):618–649
Vallar G, Bolognini N (2014) Unilateral spatial neglect. In: Nobre K, Kastner S (eds) The Oxford handbook of attention. Oxford library of psychology. Oxford University Press, New York, pp 972–1027
Vallar G, Daini R (2002) Illusions in neglect, illusions of neglect. In: Karnath HO, Milner AD, Vallar G (eds) The cognitive and neural bases of spatial neglect. Oxford University Press, New York, pp 209–224
Vallar G, Daini R, Antonucci G (2000) Processing of illusion of length in spatial hemineglect: a study of line bisection. Neuropsychologia 38(7):1087–1097
Vallar G, Bottini G, Paulesu E (2003) Neglect syndromes: the role of the parietal cortex. Adv Neurol 93:293–319
Verdon V, Schwartz S, Lovblad KO, Hauert CA, Vuilleumier P (2009) Neuroanatomy of hemispatial neglect and its functional components: a study using voxel-based lesion-symptom mapping. Brain 133(3):880–894
Weidner R, Fink GR (2006) The neural mechanisms underlying the Müller-Lyer illusion and its interaction with visuospatial judgments. Cereb Cortex 17(4):878–884
Woods AJ, Antal A, Bikson M et al (2016) A technical guide to tDCS, and related non-invasive brain stimulation tools. Clin Neurophysiol 127(2):1031–1048
Zaghi S, Acar M, Hultgren B, Boggio PS, Fregni F (2010) Noninvasive brain stimulation with low-intensity electrical currents: putative mechanisms of action for direct and alternating current stimulation. The Neuroscientist 16(3):285–307
Zavagno D (1999) Some new luminance-gradient effects. Perception 28(7):835–838
Zavagno D, Caputo G (2005) Glowing greys and surface-white: the photo-geometric factors of luminosity perception. Perception 34(3):261–274
Zavagno D, Daneyko O (2017) The glare effect. In: Shapiro AG, Todorovic D (eds) The oxford compendium of visual illusions. Oxford University Press, New York, pp 454–462
Zavagno D, Daneyko O, Sakurai K (2011) What can pictorial artifacts teach us about light and lightness? Jpn Psychol Res 53(4):448–462
Zavagno D, Tommasi L, Laeng B (2017) The eye pupil’s response to static and dynamic illusions of luminosity and darkness. i-Perception 8(4):2041669517717754
Zihl J (1995) Visual scanning behavior in patients with homonymous hemianopia. Neuropsychologia 33(3):287–303
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Maddaluno, O., Facchin, A., Zavagno, D. et al. Evidence of top-down modulation of the Brentano illusion but not of the glare effect by transcranial direct current stimulation. Exp Brain Res 237, 2111–2121 (2019). https://doi.org/10.1007/s00221-019-05577-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00221-019-05577-0