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Research

The brain’s magnetic (MEG), neurelectric (ERP), and hemodynamic (fMRI) response to novel distracting sounds recorded in our [Brain]lab
| Involuntary attention |
Our research efforts have been devoted to
two main areas of interest. One of these areas, with increasing
dedication at present, is that of the neural mechanisms of
involuntary attention. Broadly speaking, we are interested
in the cerebral mechanisms of distraction, that is, in the
cerebral regions involved, in their temporal dynamics of activation,
in pathological distraction, i.e., that resulting from brain
injury or mental, neurological or developmental disease, and
in the individual differences on distraction, specifically
those resulting from particular genetic profiles.
We have developed a laboratory task to induce
distraction under controlled conditions (Escera et al., 1998).
Briefly, subjects are instructed to press a response button
according to visual stimulus category, while ignoring concomitant
sounds, these being a repeating tone, but occasionally a deviant
tone or a unique environmental “novel” sound.
We have shown repeatedly that deviant tones and novel sounds
increase response time to subsequent visual stimuli, i.e.,
they induce distraction during subject’s task performance
(e.g., Alho et al., 1997, Escera et al., 1998, 2000, 2001,
Yago et al., 2001a, 2001b, 2003). The event-related brain
potential (ERP) recording during distraction results in a
three-phases waveform, including MMN/N1, Novelty-P3 or P3a,
and Reorienting Negativity (RON) components, these indexing,
respectively, capture, orienting and reorienting of attention.
The use of this “Distraction Potential” (DP) has
allowed us to show, for instance, that orienting of attention
towards significant stimuli takes place before semantic analysis
of the eliciting stimulus (Escera et al., 2003), or that the
common complain of increased distractibility in chronic alcoholics
may be explained by an abnormal activation of their cerebral
network controlling attention to irrelevant stimuli (Polo
et al., 2003). Nevertheless, this distractor effect can be modulated by top-down processes, referred to the so-called cognitive set (the ongoing task demands). We are currently investigating how an emotional context or different working memory loads in a task can modify this involuntary attentional capture (bottom-up processes).
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| Mismatch negativity |
We have also been interested in the clinical
applications of mismatch negativity (MMN), an ERP elicited
to auditory stimulus changes. Mostly with the support of an
European Union contract (BIOMED-2, IV Framework Programme),
our studies have dealt with the individual replicability of
MMN (see Escera & Grau, 1996, Escera et al., 2000), the
development of new MMN paradigms, specifically to test auditory
sensory memory (e.g., Grau et al., 1998), the application
of these paradigms to chronic alcoholism (Polo et al., 1999;
Grau et al., 2001), and the relationships of MMN with conscious
perception of sound changes (e.g., Amenedo & Escera, 2000).
In this area of research, we are currently working in the
development of protocols to assess central sound representation,
and in their application to various developmental disorders,
such as stuttering and dyslexia. Moreover, we are now working,
with the MMN, on the brain mechanisms of abstract acoustic
object formation, and on the interaction between the auditory
and visual modalities in auditory perception.
See the individual pages of lab members
for further details and current projects!
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| Equipment and facilities |
We still use our old SynAmps amplifier with 32
channels (Neuroscan, USA), but we have now access to a brand
new 64 channels eemagine system from ANT Software (The Netherlands), and to Advanced Source Analysis
(ASA) software, also from ANT. And we have also access to the
MEG equipment of our collaborators Tomás Ortiz in Madrid
(Spain) and Hirooki Yabe in Hirosaki (Japan) and functional magnetic resonance imaging (fMRI) from our colleague Manfred Herrmann in Bremen (Germany).
Lab 1
Lab 2
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