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Today’s cognitive science largely follows the tradition of empiricism by looking for correspondences between ‘stimuli’ in the external world and their responses or ‘representation’ in the brain. This approach works well (sort of) in primary sensory areas but typically fails when cognitive, emotional mechanisms are to be investigated. The empiricist method is a bit like learning words of a foreign language, i.e., collecting correspondences between a known and a new language. The initial progress is fast; one can get by in Hungary with just 100 words of vocabulary. However, when it comes to a true understanding of an unknown language, such as a hieroglyphs or the language of the brain, one needs to know about the grammar, the syntactical rules that allow for the generation of a virtually infinite number of combinations from a finite number of lexical elements using a minimal number of rules. Syntax allows for segmentation of information (tempo, punctuation, etc), temporal progression of discrete elements into ordered and hierarchical relations, resulting in congruent interpretation of meaning.

I try to understand the brain, using this ‘inside-out’ approach by investigating “neural syntax”. In brain networks, especially those serving cognitive functions, packaging and segmentation of neural information is supported by the numerous rhythms the brain generates. Brain rhythms provide temporal correlations at multiple time scales, which can be mathematically defined. Rhythms and other non-rhythmic ‘chunking’ patterns can be conceived of as ‘order parameters’ and often recognized in the local field potentials. These mesoscopic patterns are the telltale of grouping and segregation of transient cell assemblies and their evolving sequences. Work in my lab focuses largely on the generation of these various oscillations, their spatial and temporal relationships, and the role of inhibition in the enforcement of syntactic rules. These mesoscopic temporal structures are fully preserved throughout the mammalian evolution and constrain both evolutionary and ontogenetic scaling of brain structures. We monitor large-scale neuronal firing patterns and the local fields they generate in behaving rodents and relate the assembly patterns and order parameters to overt and covert behaviors. The advantage of our ‘inside-out’ approach to brain function is that it is free of philosophical connotations and takes brain mechanisms as independent variables, as opposed to attempts to find ‘correspondences’ or ‘representations’ between subjectively derived categories and boundaries and brain responses. If you remain skeptic of our approach, just ask any practicing psychiatrist how well the boundaries set up by DSM-IV translate to the diseases they treat.

Clayton Curtis

Psychology Department
 
 
 
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