\ Erisir Lab Webpage

Alev Erisir, PhD

Professor & Chair

Department of Psychology

102/187/079 Gilmer Hall


Synaptic connections among neurons that make up sensory pathways and other functional circuitries are the building blocks for how our brain functions, or in other words, how we see, hear, taste, move, learn, make plans or remember. These connections are amanable to change throughout life, allowing us to learn new skills, or to adapt to any external or internal alteration, including as we grow or age. By studying the morphological properties of neurons, synapses and identified axons, we aim to understand the synaptic inputs that converge on functionally distinct brain nuclei, how those inputs develop to form functional circuitries of the adult brain, and how they re-wire or degenerate. What are the mechanisms by which the critical period of developmental plasticity is initiated, and terminated? Is there a change in the neurotransmitters, neuromodulators, hormones or their receptors that can signal the changes in sensory perception or the behavior? How do glial cells interact with neurons in developing or aging brains? Using anatomical techniques including immuno-electron microscopy, ultrastructural morphometry, tract-tracing and confocal microscopy, we study synaptic curcuitries in visual and gustatory sensory pathways during postnatal development, healthy adulthood and aging stages of our life span.

Input Selectivity of Inputs on Dendrite Segments in the Visual Thalamus

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Taste Patways and Behavior in the Tree Shrew (Tupaia Belangeri)

We use tree shrews, the closest relative of the primates and a versatile animal model to study sensory systems, to understand the organization and the plasticitiy of taste system.

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Synaptic Circuitry in Gustatory Thalamus

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Efferent Convergence in Gustatory Brainstem

High resolution confocal microsopy is used to identify putative synapses between neuronal elements idemtified by multi-tract tracing aproaches.

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Ultrastructural Neuropathology in Alzheimer's Models

In most transgenic models of the Alzheimer's Disease, behavioral deficits onset months before any of the hallmark lesions, amyloid plaques or neurofibrillary tangles are detected. We use electron microscopy to indentify early pathological alterations.
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