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D S Touretzky

Publications and source records attributed to D S Touretzky.

7 recordsLinked to original sources

Modeling attractor deformation in the rodent head-direction system.

We present a model of the head-direction circuit in the rat that improves on earlier models in several respects. First, it provides an account of some of the unique characteristics of head-direction (HD) cell firing in the lateral mammillary nucleus and the anterior thalamus. Second, the model functions without making physiologically unrealistic assumptions. In particular, it implements attractor dynamics in postsubiculum and lateral mammillary nucleus without directionally tuned inhibitory neurons, which have never been observed in vivo, and it integrates angular velocity without the use of multiplicative synapses. The model allows us to examine the relationships among three HD areas and various properties of their representations. A surprising result is that certain combinations of purported HD cell properties are mutually incompatible, suggesting that the lateral mammillary nucleus may not be the primary source of head direction input to anterior thalamic HD cells.

Algorithms↗

The role of the hippocampus in solving the Morris water maze.

We suggest that the hippocampus plays two roles that allow rodents to solve the hidden-platform water maze: self-localization and route replay. When an animal explores an environment such as the water maze, the combination of place fields and correlational (Hebbian) long-term potentiation produces a weight matrix in the CA3 recurrent collaterals such that cells with overlapping place fields are more strongly interconnected than cells with nonoverlapping fields. When combined with global inhibition, this forms an attractor with coherent representations of position as stable states. When biased by local view information, this allows the animal to determine its position relative to the goal when it returns to the environment. We call this self-localization. When an animal traces specific routes within an environment, the weights in the CA3 recurrent collaterals become asymmetric. We show that this stores these routes in the recurrent collaterals. When primed with noise in the absence of sensory input, a coherent representation of position still forms in the CA3 population, but then that representation drifts, retracing a route. We show that these two mechanisms can coexist and form a basis for memory consolidation, explaining the anterograde and limited retrograde amnesia seen following hippocampal lesions.

Amnesia↗

Cognitive maps beyond the hippocampus.

We present a conceptual framework for the role of the hippocampus and its afferent and efferent structures in rodent navigation. Our proposal is compatible with the behavioral, neurophysiological, anatomical, and neuropharmacological literature, and suggests a number of practical experiments that could support or refute it. We begin with a review of place cells and how the place code for an environment might be aligned with sensory cues and updated by self-motion information. The existence of place fields in the dark suggests that location information is maintained by path integration, which requires an internal representation of direction of motion. This leads to a consideration of the organization of the rodent head direction system, and thence into a discussion of the computational structure and anatomical locus of the path integrator. If the place code is used in navigation, there must be a mechanism for selecting an action based on this information. We review evidence that the nucleus accumbens subserves this function. From there, we move to interactions between the hippocampal system and the environment, emphasizing mechanisms for learning novel environments and for aligning the various subsystems upon re-entry into familiar environments. We conclude with a discussion of the relationship between navigation and declarative memory.

Acetylcholine↗

A parallel licensing model of normal slips and phonemic paraphasias.

A model of phonological processing in speech production based on prosodic licensing can capture general patterns of errors found in both normal and aphasic speech. All segments must be licensed by some prosodic category (syllable, nucleus, or rime) in order to be produced. Constraints on licensing, including both phonotactic and binding constraints, ensure that only correct licensing associations are retained. A computer simulation of our model produces utterances in qualitative agreement with human speech error data. Phonemic puraphasias are claimed to arise from the same mechanisms as normal speech errors; the difference being only a matter of disturbance of the lexical retrieval and licensing processes. The fact that these errors, which can involve gross disruption of the segmental sequence, still produce phonotactically well-formed strings is a direct consequence of the syllabic licensing that forms the core of our theory of speech production.

Aphasia↗

Theory of rodent navigation based on interacting representations of space.

We present a computational theory of navigation in rodents based on interacting representations of place, head direction, and local view. An associated computer model is able to replicate a variety of behavioral and neurophysiological results from the rodent navigation literature. The theory and model generate predictions that are testable with current technologies.

Animals↗

The reaching task: evidence for vector arithmetic in the motor system?

During a reaching task, the population vector is an encoding of direction based on cells with cosine response functions. Scaling the response by a magnitude factor produces a vector encoding, enabling vector arithmetic to be performed by the summation of firing rates. We show that the response properties of selected populations of cells in the primary motor cortex and area 5 can be explained in terms of arithmetic relationships among load, goal, and motor command vectors. Our computer simulations show good agreement with single-cell recording data.

Animals↗