The Journal of Neurophysiology Vol. 83 No. 1 January 2000, pp. 90-98
Copyright ©2000 by the American Physiological Society

Cumulative Effects of Glutamate Microstimulation on Ca²⁺ Responses of CA1 Hippocampal Pyramidal Neurons in Slice

Department of Neuroscience, University of New Mexico School of Medicine, Albuquerque, New Mexico 87131

Connor, John A. and Robert J. Cormier. Cumulative Effects of Glutamate Microstimulation on Ca²⁺ Responses of CA1 Hippocampal Pyramidal Neurons in Slice. J. Neurophysiol. 83: 90-98, 2000. Glutamate stimulation of hippocampal CA1 neurons in slice was delivered via iontophoresis from a microelectrode. Five pulses (~5 µA, 10 s duration, repeated at 1 min intervals) were applied with the electrode tip positioned in the stratum radiatum near the dendrites of a neuron filled with the Ca²⁺ indicator fura-2. A single stimulus set produced Ca²⁺ elevations that ranged from several hundred nM to several µM and that, in all but a few neurons, recovered within 1 min of stimulus termination. Subsequent identical stimulation produced Ca²⁺ elevations that outlasted the local glutamate elevations by several minutes as judged by response recoveries in neighboring cells or in other parts of the same neuron. These long responses ultimately recovered but persisted for up to 10 min and were most prominent in the mid and distal dendrites. Recovery was not observed for responses that spread to the soma. The elevated Ca²⁺ levels were accompanied by membrane depolarization but did not appear to depend on the depolarization. High-resolution images demonstrated responsive areas that involved only a few µm of dendrite. Our results confirm the previous general findings from isolated and cell culture neurons that glutamate stimulation, if carried beyond a certain range, results in long-lasting Ca²⁺ elevation. The response characterized here in mature in situ neurons was significantly different in terms of time course and reversibility. We suggest that the extended Ca²⁺ elevations might serve not only as a trigger for delayed neuron death but, where more spatially restricted, as a signal for local remodeling in dendrites.