| Literature DB >> 16759399 |
Georg Northoff1, Alexander Heinzel.
Abstract
Though the brain and its neuronal states have been investigated extensively, the neural correlates of mental states remain to be determined. Since mental states are experienced in first-person perspective and neuronal states are observed in third-person perspective, a special method must be developed for linking both states and their respective perspectives. We suggest that such method is provided by First-Person Neuroscience. What is First-Person Neuroscience? We define First-Person Neuroscience as investigation of neuronal states under guidance of and on orientation to mental states. An empirical example of such methodological approach is demonstrated by an fMRI study on emotions. It is shown that third- and first-person analysis of data yield different results. First-person analysis reveals neural activity in cortical midline structures during subjective emotional experience. Based on these and other results neural processing in cortical midline structures is hypothesized to be crucially involved in generating mental states. Such direct linkage between first- and third-person approaches to analysis of neural data allows insight into the "point of view from within the brain", that is what we call the First-Brain Perspective. In conclusion, First-Person Neuroscience and First-Brain Perspective provide valuable methodological tools for revealing the neuronal correlate of mental states.Entities:
Year: 2006 PMID: 16759399 PMCID: PMC1459272 DOI: 10.1186/1747-5341-1-3
Source DB: PubMed Journal: Philos Ethics Humanit Med ISSN: 1747-5341 Impact factor: 2.464
Figure 1Linkage between mental and neuronal states in "First-Person Neuroscience".
Signal changes as obtained in categorical or third-person and parametric or first-person analysis.
| Signal changes in categorical analysis (third-person) | Signal changes in parametric analysis (first-person) | |
| Orbitomedial prefrontal cortex (OMPFC) | -2/54/14, 3.65 | 16/56/19, 3.35 |
| Dorsomedial prefrontal cortex (DMPFC) | 4/48/40, 3.68 | 12/48/24, 3.29 |
| Medial parietal cortex (MPC) | - | -2/-34/60, 3.68 |
| Insula | - | -54/-10/14, 4.32 |
| Bilateral posterior parietal cortex | -48/-67/28, 3.36; 50/-63/25, 3.34 | - |
| Thalamus/Hypothalamus | 0/-8/4, 3.39 | - |
| Posterior cingulate | 0/-38/40, 3.83 | - |
X, y, z: MNI coordinates in mm. X describes right (+)/left (-), y anterior (+)/posterior (-), and z superior (+)/inferior (-) distances (e.g. 21/23/43, 3.45 ≅ x = 21/y = 23/z = 43, Z = 3.45). Coordinates of the local maxima of regional signal increases are given. Z = Z-score. Only signal increases with Z > 3.29 (p < 0.001, uncorrected, voxel level) are described.
Signal changes associated with categorical analysis reflect the comparison between the IAPS picture categories and the baseline condition. (Left column)
In contrast, the parametric analysis tested for a linear relationship between regional changes in the BOLD signal and valence of the presented IAPS pictures as rated by the investigated subjects. The IAPS pictures were modeled as a regressor according to their valence ranging from 1 to 9. The parametric signal changes were tested against the baseline condition. Regions are listed that show a positive linear relationship between valence and BOLD signal changes. (Right column)
Note the overlap between both comparisons with regard to involvement of OMPFC and DMPFC. The other regions, in contrast, were either involved in categorical or parametric analysis.
Figure 2Parametric or first-person modulation in cortical midline regions during emotional picture presentation. a) Upper part. FMRI images represent results from a random effects group analysis (n = 13) depicted on a standard MNI brain. X, y, z: MNI coordinates in mm. X describes right (+)/left (-), y anterior (+)/posterior (-), and z superior (+)/inferior (-) distances. Z = Z-score. Only regions with Z > 3.29 (p < 0.001, uncorrected, voxel level) are described. The aim of the analysis was to characterise the parametric modulation of the BOLD-signal during the presentation of IAPS-pictures. To that end we adopted a parametric analysis using the valence ratings (1–9 rated by the subjects in a post hoc analysis) as the modulation parameter, which was tested against baseline. Parametric modulations of regional signal intensities during presentation of IAPS pictures were obtained in OMPFC (x = 16, y = 56, z = 19; Z = 3.35), DMPFC (x = 12, y = 48, z = 24; Z = 3.29; visible in the coronal image), MPC (x = -2, y = 34, z = 60; Z = 3.68) and left insula (x = -54, y = -10, z = 14; Z = 4.3). b) Lower Part. The parametric relationship between picture valence (x-axis, valence values from 1 [negative] to 9 [positive]) and signal percent change (y-axis, intensity change of the BOLD signal) during viewing of IAPS pictures is demonstrated. The regional local maxima of valence-dependent modulation were correlated with the picture valences. Parametric valence-dependent modulation of signal percent change was found in the following regions during IAPS picture viewing: The OMPFC (x = 16, y = 56, z = 19; Z = 3.35), the DMPFC (x = 12, y = 48, z = 24; Z = 3.29) and the MPC (x = -2, y = -34, z = 60; Z = 3.68). OMPFC = orbitomedial prefrontal cortex, DMPFC = dorsomedial prefrontal cortex, MPC = medial parietal cortex.
Figure 3First-Person Perspective.
Figure 4Third-Person Perspective.
Figure 5First-Brain Perspective.