David B. Jaffe, Ph.D.
Phone: (210) 458-5843
Areas of Specialization
» Hippocampal function and Alzheimer’s disease
» Post-traumatic stress disorder
» Synaptic and axonal signal integration
Ph.D. in Neuroscience; Baylor College of Medicine
M.S. in Physiology; Duke University
B.A. in Biochemistry; University of Texas at Austin
B.S. in Zoology; University of Texas at Austin
Research in Dr. Jaffe’s lab focuses on the hippocampal formation; a brain region important for certain aspects of learning and memory. It is also one of the first brain structures affected by Alzheimer's disease and medial temporal lobe epilepsy arises in the hippocampus, among other brain structures.
The lab’s major area of interest is the CA3 region of the hippocampus. This subregion is where information from two regions outside the hippocampus, the dentate gyrus and the entorhinal cortex, converge. In addition, this area is also characterized by strong recurrent feedback between CA3 pyramidal neurons forming what is thought to be an autoassociative network. Artificial neural networks composed of such circuits perform pattern completion. Under pathological conditions, this circuity is what makes area CA3 highly susceptible to epilepsy.
Current work in the lab focuses on two questions:
- What are the input/output characteristics of CA3 pyramidal neurons? The lab is interested in how the morphology and distribution of ion channels in these cells interact to process, encode, and retrieve synaptically-based information. Understanding how these cells integrate synaptic information is important for understanding the functional role of this network during normal circumstances and under pathophysiological conditions, for example in the case of epilepsy.
- How the properties of neurons and synapses within area CA3 change in aged animals. It is well known that aged animals are cognitively impaired and this correlates with a number of cellular changes that occur with senescence. The lab is testing whether some of these changes might actually be compensatory. That is, in response to pathophysiological changes that occur with age, such as the loss of receptors associated with synaptic, certain changes in excitability or synaptic inhibition may enhance functional aspects of the network as it ages.
Click here for a list of publications.