Short-term plasticity of visuo-haptic object recognition
Functional magnetic resonance imaging (fMRI) studies have provided ample evidence for the involvement of the lateral occipital cortex (LO), fusiform gyrus (FG), and intraparietal sulcus (IPS) in visuo-haptic object integration. Here we applied 30 min of sham (non-effective) or real offline 1 Hz repe...
| Main Authors: | , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2014-04-01
|
| Series: | Frontiers in Psychology |
| Subjects: | |
| Online Access: | http://journal.frontiersin.org/Journal/10.3389/fpsyg.2014.00274/full |
| _version_ | 1818028205551910912 |
|---|---|
| author | Tanja eKassuba Tanja eKassuba Tanja eKassuba Corinna eKlinge Corinna eKlinge Cordula eHölig Cordula eHölig Brigitte eRöder Hartwig Roman Siebner Hartwig Roman Siebner Hartwig Roman Siebner |
| author_facet | Tanja eKassuba Tanja eKassuba Tanja eKassuba Corinna eKlinge Corinna eKlinge Cordula eHölig Cordula eHölig Brigitte eRöder Hartwig Roman Siebner Hartwig Roman Siebner Hartwig Roman Siebner |
| author_sort | Tanja eKassuba |
| collection | DOAJ |
| description | Functional magnetic resonance imaging (fMRI) studies have provided ample evidence for the involvement of the lateral occipital cortex (LO), fusiform gyrus (FG), and intraparietal sulcus (IPS) in visuo-haptic object integration. Here we applied 30 min of sham (non-effective) or real offline 1 Hz repetitive transcranial magnetic stimulation (rTMS) to perturb neural processing in left LO immediately before subjects performed a visuo-haptic delayed-match-to-sample task during fMRI. In this task, subjects had to match sample (S1) and target (S2) objects presented sequentially within or across vision and/or haptics in both directions (visual-haptic or haptic-visual) and decide whether or not S1 and S2 were the same objects. Real rTMS transiently decreased activity at the site of stimulation and remote regions such as the right LO and bilateral FG during haptic S1 processing. Without affecting behavior, the same stimulation gave rise to relative increases in activation during S2 processing in the right LO, left FG, bilateral IPS, and other regions previously associated with object recognition. Critically, the modality of S2 determined which regions were recruited after rTMS. Relative to sham rTMS, real rTMS induced increased activations during crossmodal congruent matching in the left FG for haptic S2 and the temporal pole for visual S2. In addition, we found stronger activations for incongruent than congruent matching in the right anterior parahippocampus and middle frontal gyrus for crossmodal matching of haptic S2 and in the left FG and bilateral IPS for unimodal matching of visual S2, only after real but not sham rTMS. The results imply that a focal perturbation of the left LO triggers modality-specific interactions between the stimulated left LO and other key regions of object processing possibly to maintain unimpaired object recognition. This suggests that visual and haptic processing engage partially distinct brain networks during visuo-haptic object matching. |
| first_indexed | 2024-12-10T05:00:06Z |
| format | Article |
| id | doaj.art-ef80d6c445674bd19d1b63a0ef9d3e94 |
| institution | Directory Open Access Journal |
| issn | 1664-1078 |
| language | English |
| last_indexed | 2024-12-10T05:00:06Z |
| publishDate | 2014-04-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Psychology |
| spelling | doaj.art-ef80d6c445674bd19d1b63a0ef9d3e942022-12-22T02:01:25ZengFrontiers Media S.A.Frontiers in Psychology1664-10782014-04-01510.3389/fpsyg.2014.0027478422Short-term plasticity of visuo-haptic object recognitionTanja eKassuba0Tanja eKassuba1Tanja eKassuba2Corinna eKlinge3Corinna eKlinge4Cordula eHölig5Cordula eHölig6Brigitte eRöder7Hartwig Roman Siebner8Hartwig Roman Siebner9Hartwig Roman Siebner10Copenhagen University Hospital HvidovreUniversity Medical Center Hamburg-EppendorfChristian-Albrechts-UniversityUniversity Medical Center Hamburg-EppendorfWarneford HospitalUniversity Medical Center Hamburg-EppendorfUniversity of HamburgUniversity of HamburgCopenhagen University Hospital HvidovreUniversity Medical Center Hamburg-EppendorfChristian-Albrechts-UniversityFunctional magnetic resonance imaging (fMRI) studies have provided ample evidence for the involvement of the lateral occipital cortex (LO), fusiform gyrus (FG), and intraparietal sulcus (IPS) in visuo-haptic object integration. Here we applied 30 min of sham (non-effective) or real offline 1 Hz repetitive transcranial magnetic stimulation (rTMS) to perturb neural processing in left LO immediately before subjects performed a visuo-haptic delayed-match-to-sample task during fMRI. In this task, subjects had to match sample (S1) and target (S2) objects presented sequentially within or across vision and/or haptics in both directions (visual-haptic or haptic-visual) and decide whether or not S1 and S2 were the same objects. Real rTMS transiently decreased activity at the site of stimulation and remote regions such as the right LO and bilateral FG during haptic S1 processing. Without affecting behavior, the same stimulation gave rise to relative increases in activation during S2 processing in the right LO, left FG, bilateral IPS, and other regions previously associated with object recognition. Critically, the modality of S2 determined which regions were recruited after rTMS. Relative to sham rTMS, real rTMS induced increased activations during crossmodal congruent matching in the left FG for haptic S2 and the temporal pole for visual S2. In addition, we found stronger activations for incongruent than congruent matching in the right anterior parahippocampus and middle frontal gyrus for crossmodal matching of haptic S2 and in the left FG and bilateral IPS for unimodal matching of visual S2, only after real but not sham rTMS. The results imply that a focal perturbation of the left LO triggers modality-specific interactions between the stimulated left LO and other key regions of object processing possibly to maintain unimpaired object recognition. This suggests that visual and haptic processing engage partially distinct brain networks during visuo-haptic object matching.http://journal.frontiersin.org/Journal/10.3389/fpsyg.2014.00274/fullVisual Perceptionfunctional magnetic resonance imagingobject recognitionrepetitive transcranial magnetic stimulationMultisensory Interactionshaptic perception |
| spellingShingle | Tanja eKassuba Tanja eKassuba Tanja eKassuba Corinna eKlinge Corinna eKlinge Cordula eHölig Cordula eHölig Brigitte eRöder Hartwig Roman Siebner Hartwig Roman Siebner Hartwig Roman Siebner Short-term plasticity of visuo-haptic object recognition Frontiers in Psychology Visual Perception functional magnetic resonance imaging object recognition repetitive transcranial magnetic stimulation Multisensory Interactions haptic perception |
| title | Short-term plasticity of visuo-haptic object recognition |
| title_full | Short-term plasticity of visuo-haptic object recognition |
| title_fullStr | Short-term plasticity of visuo-haptic object recognition |
| title_full_unstemmed | Short-term plasticity of visuo-haptic object recognition |
| title_short | Short-term plasticity of visuo-haptic object recognition |
| title_sort | short term plasticity of visuo haptic object recognition |
| topic | Visual Perception functional magnetic resonance imaging object recognition repetitive transcranial magnetic stimulation Multisensory Interactions haptic perception |
| url | http://journal.frontiersin.org/Journal/10.3389/fpsyg.2014.00274/full |
| work_keys_str_mv | AT tanjaekassuba shorttermplasticityofvisuohapticobjectrecognition AT tanjaekassuba shorttermplasticityofvisuohapticobjectrecognition AT tanjaekassuba shorttermplasticityofvisuohapticobjectrecognition AT corinnaeklinge shorttermplasticityofvisuohapticobjectrecognition AT corinnaeklinge shorttermplasticityofvisuohapticobjectrecognition AT cordulaeholig shorttermplasticityofvisuohapticobjectrecognition AT cordulaeholig shorttermplasticityofvisuohapticobjectrecognition AT brigitteeroder shorttermplasticityofvisuohapticobjectrecognition AT hartwigromansiebner shorttermplasticityofvisuohapticobjectrecognition AT hartwigromansiebner shorttermplasticityofvisuohapticobjectrecognition AT hartwigromansiebner shorttermplasticityofvisuohapticobjectrecognition |