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Facing facts: Neuronal mechanisms of face perception

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Dekowska M., Kuniecki M., Jaskowski P.
Acta Neurobiologiae Experimentalis
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2008
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vol. 68
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issue 2
229-252
EN
The face is one of the most important stimuli carrying social meaning. Thanks to the fast analysis of faces, we are able to judge physical attractiveness and features of their owners' personality, intentions, and mood. From one's facial expression we can gain information about danger present in the environment. It is obvious that the ability to process efficiently one's face is crucial for survival. Therefore, it seems natural that in the human brain there exist structures specialized for face processing. In this article, we present recent findings from studies on the neuronal mechanisms of face perception and recognition in the light of current theoretical models. Results from brain imaging (fMRI, PET) and electrophysiology (ERP, MEG) show that in face perception particular regions (i.e. FFA, STS, IOA, AMTG, prefrontal and orbitofrontal cortex) are involved. These results are confirmed by behavioral data and clinical observations as well as by animal studies. The developmental findings reviewed in this article lead us to suppose that the ability to analyze face-like stimuli is hard-wired and improves during development. Still, experience with faces is not sufficient for an individual to become an expert in face perception. This thesis is supported by the investigation of individuals with developmental disabilities, especially with autistic spectrum disorders (ASD).
2
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The P3 produced by auditory stimuli presented in a passive and active condition: modulation by visual stimuli

100%
Wronka E., Kuniecki M., Kaiser J., Coenen A. M.
Acta Neurobiologiae Experimentalis
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2007
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vol. 67
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issue 2
155-164
EN
The aim of this study was to investigate how the processing of auditory stimuli is affected by the simultaneous presentation of visual stimuli. This was approached in an active and passive condition, during which a P3 was elicited in the human EEG by single auditory stimuli. Subjects were presented tones, either alone or accompanied by the simultaneous exposition of pictures. There were two different sessions. In the first, the presented tones demanded no further cognitive activity from the subjects (passive or 'ignore' session), while in the second session subjects were instructed to count the tones (active or 'count' session). The central question was whether inter-modal influences of visual stimulation in the active condition would modulate the auditory P3 in the same way as in the passive condition. Brain responses in the ignore session revealed only a small P3-like component over the parietal and frontal cortex, however, when the auditory stimuli co-occurred with the visual stimuli, an increased frontal activity in the window of 300-500 ms was observed. This could be interpreted as the reflection of a more intensive involuntary attention shift, provoked by the preceding visual stimulation. Moreover, it was found that cognitive load caused by the count instruction, resulted in an evident P3, with maximal amplitude over parietal locations. This effect was smaller when auditory stimuli were presented on the visual background. These findings might support the thesis that available resources were assigned to the analysis of visual stimulus, and thus were not available to analyze the subsequent auditory stimuli. This reduction in allocation of resources for attention was restricted to the active condition only, when the matching of a template with incoming information results in a distinct P3 component. It is discussed whether the putative source of this effect is a change in the activity of the frontal cortex.
3
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Correlation between long latency evoked potentials from amygdala and evoked cardiac response to fear conditioned stimulus in rats

100%
Kuniecki M., Coenen A. M. l., Kaiser J.
Acta Neurobiologiae Experimentalis
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2002
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vol. 62
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issue 2
85-92
EN
We investigated relation between activity of central nucleus of amygdala (CE) and phasic heart rate deceleration during differential fear conditioning. We found that P2 component of long-lasting event potential (EP) to CS+ but not to CS- correlated strongly with HR deceleration in the 1st second after stimulus onset. Obtained results are discussed in the light of LeDoux?s and Kapp?s findings showing crucial role of amygdala in processing of emotionally relevant stimulation and it?s involvement in initiating autonomic responses.
4
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Central control of heart rate changes during visual affective processing as revealed by fMRI

88%
Kuniecki M., Urbanik A., Sobiecka B., Kozub J., Binder M.
Acta Neurobiologiae Experimentalis
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2003
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vol. 63
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issue 1
39-48
EN
In the present study we addressed the question of central control of heart rate (HR) in emotions. Parallel measurement of HR changes and changes of local intensity of blood flow as indexed by fMRI in a procedure eliciting emotions allowed us to pinpoint areas of the brain responsible for HR variations during emotional arousal. In condition eliciting positive emotions we detected activation of occipito-temporal regions, anterior insula, and hypothalamus. In condition eliciting negative emotions we also detected activation of occipito-temporal regions and additionally activation of bilateral anterior insulae, right amygdala and right superior temporal gyrus. The results show that structures constituting neural network involved in HR control during emotional arousal are affect specific. Particularly the central circuit controlling HR in negative affect includes the amygdala, while central circuit controlling HR in positive affect includes the hypothalamus. Additionally activation of bilateral occipito-temporal cortex proves enhancement of visual processing of emotional material as compared to neutral material in both positive and negative affect. This might be attributed to top-down processes originating in the frontal lobe and related to shifting attention to the emotionally relevant stimuli. Activation of insular cortex is probably related to autonomic arousal accompanying watching emotional content (e.g. sweating, heart-rate changes etc.). Activation of the amygdala in the negative condition supports the well documented engagement of this structure in processing of fear and disgust.
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