SUNY Downstate Health Sciences University
Department of Physiology and Pharmacology
Armin Stelzer, MD, PhD
Physiology and Pharmacology
Tel: (718) 270-3873
Activity-Dependent Modification of Cortical Responses
Our lab studies mechanisms of activity-dependent plasticity of the central nervous system. Plasticity represents a modification of cellular and population activity in response to activation in certain brain areas. The main focus is the study of underlying mechanisms of a model of learning and memory, called long-term potentiation (LTP).
Calcium-dependent changes in the efficacy of ligand-gated receptors. Whole-cell clamp experiments are performed in acutely dissociated pyramidal cells of the hippocampus and pyramidal cells in the CA1 region of the hippocampal slice. Effects of elevation of intracellular calcium on GABAA and AMPA receptor function are measured. GABAA and AMPA receptors are the receptors mediating fast synaptic inhibition and excitation, resp. in the mammalian CNS. Sources of elevation of Ca2+ are the experimental internal perfusion of solutions containing defined Ca2+ levels and calcium transients through voltage-gated calcium channels and NMDA receptor-coupled channels. The experiments also address the biochemical mechanisms of elevation of Ca2+ in the regulation of AMPA and GABAA receptor function. Possible roles of enzymes that are known to be activated by Ca2+ are examined.
Activity-dependent changes of synaptic plasticity. Experiments in CA1 pyramidal cells of the hippocampal slice preparation examine activity-dependent long term modification of the inhibitory circuitry. Parameters of fast synaptic inhibition (IPSP, IPSC, inhibitory conductances) are measured at various points of time following application of high-frequency trains of stimuli that is known to generate long-term potentiation of excitatory responses (LTP). Intracellular recordings in CA1 pyramidal cells examine a possible role of a long-term decrease of synaptic inhibition as an underlying mechanism of pyramidal cell LTP. (see Figure 1)
Bin Hu, M.D., Research Associate
- Stelzer, A., Slater, N. T., and ten Bruggencate, C. (1987). Activation of NMDA receptors blocks GABAergic inhibition in an in vitro model of epilepsy. Nature 326, 698-701.
- Stelzer, A., Kay, A. R., and Wong, R. K. S. (1988). GABAA receptor function in hippocampal cells is maintained by phosphorylation factors. Science 241, 339-341.
- Stelzer, A., Simon, G., Kovacs, G., and Rai, R. (1994). Synaptic disinhibition during maintenance of long-term potentiation in CA1 pyramidal cells. Proc. Nat. Acad. Sci. USA 91, 3058-3062.
- Karnup, S. V., and Stelzer, A. (1999). Temporal overlap of excitatory and inhibitory afferent input in guinea-pig CA1 pyramidal cells. J. Physiol. 516, 485-504.
- Karnup, S. V., and Stelzer, A. (2001). Seizure-like activity in the disinhibited CA1 minislice of adult guinea pigs. J. Physiol. 523, 713-730.