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  • Fidel Santamaria, Ph.D.
Fidel Santamaria

Contact

210-458-6910

fidel.santamaria@utsa.edu

Programs

M.S. in Biomedical Engineering
Ph.D. in Biomedical Engineering

Currently seeking M.S. students.

Fidel  Santamaria, Ph.D.

Associate Professor

Department of Biomedical Engineering

UTSA

Neuroscience

Computational neuroscience, cerebellar function in health and disease, autism

My objective is to understand how evolutionary pressure has resulted in complex neuronal functions that implement efficient coding of sensory stimuli. For this purpose, I use a combination of experimental, computational, and theoretical techniques. While most of my experimental work is centered in studying the function of the mammalian cerebellum, my modeling and theoretical work can be applied to many areas of the nervous system. My recent theoretical work has centered on developing a unified framework to study history dependence activity in the nervous system. We have shown that fractional order differential equations are the natural mathematical tools to describe history dependence. We have applied them to study the diffusion of synaptic receptors in the membrane and the generation of complex spiking patterns in whole neurons. We have recently extended our efforts to understand how history dependence affects information rates in neuronal networks. We have gone a step further by building circuits that model spiking neurons with history-dependent components, in our case capacitors that retain memory (mem-capacitors). This work falls in the context of the re-invigorated field of neuromorphic engineering, which is starting to use mem-ristors to implement history dependent learning rules.  My experimental work also looks at history dependence but from the point of intrinsic excitability in cells. In this case, we combine electrophysiology, two-photon imaging, and biophysical modeling to understand the computational function of changes in intrinsic excitability in cerebellar Purkinje cells. We have shown that intrinsic excitability changes after induction of synaptic plasticity. We have shown that intracellular calcium dynamics also changes after induction of synaptic plasticity. We suspect that the combination of synaptic and intrinsic plasticity in Purkinje cells implements a mechanism of pattern separation. More recently, we have started to study cerebellar intrinsic excitability in an animal model of Autism. 

Related Diseases: Autism, ataxia

Techniques: Neurophysiology, two-photon, modeling, theory.

Visit Dr. Fidel Santamaria's Lab »

  • Research & Grants

    My objective is to understand how evolutionary pressure has resulted in complex neuronal functions that implement efficient coding of sensory stimuli. For this purpose, I use a combination of experimental, computational, and theoretical techniques. While most of my experimental work is centered in studying the function of the mammalian cerebellum, my modeling and theoretical work can be applied to many areas of the nervous system. My recent theoretical work has centered in developing a unified framework to study history dependence activity in the nervous system. We have shown that fractional order differential equations are the natural mathematical tools to describe history dependence. We have applied them to study the diffusion of synaptic receptors in the membrane and the generation of complex spiking patterns in whole neurons. We have recently extended our efforts to understand how history dependence affects information rates in neuronal networks. We have gone a step further by building circuits that model spiking neurons with history dependent components, in our case capacitors that retain memory (mem-capacitors). This work falls in the context of the re-invigorated field of neuromorphic engineering, which is starting to use mem-ristors to implement history dependent learning rules. My experimental work also looks at history dependence but from the point of intrinsic excitability in cells. In this case, we combine electrophysiology, two-photon imaging, and biophysical modeling to understand the computational function of changes in intrinsic excitability in cerebellar Purkinje cells. We have shown that intrinsic excitability changes after induction of synaptic plasticity. We have shown that intracellular calcium dynamics also changes after induction of synaptic plasticity. We suspect that the combination of synaptic and intrinsic plasticity in Purkinje cells implements a mechanism of pattern separation. More recently, we have started to study cerebellar intrinsic excitability in an animal model of Autism.

    Sub-field: Computational neuroscience, cerebellar function in health and disease, autism

    Related Diseases: Autism and Ataxia

    Techniques: Neurphysiology, two-photon, modeling, and theory

  • Publications

    Click here for a list of publications.

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Graduate School of Biomedical Sciences

7703 Floyd Curl Drive

San Antonio, TX 78229

210-567-3709

gsbs@uthscsa.edu

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