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Volume 17, Number 8,
Issue of April 15, 1997
pp. 2900-2913
Copyright ©1997 Society for Neuroscience
A Simplified Preparation for Relating Cellular Events to
Behavior: Contribution of LE and Unidentified Siphon Sensory Neurons to
Mediation and Habituation of the Aplysia Gill- and
Siphon-Withdrawal Reflex
Received Sept. 20, 1996; revised Jan. 2, 1997; accepted Jan. 31, 1997.
Lina Frost1,
Saul W. Kaplan1,
Tracey E. Cohen1,
Victor Henzi1,
Eric R. Kandel1, 2, 3, and
Robert D. Hawkins1, 2
1 Center for Neurobiology and Behavior, College of
Physicians and Surgeons of Columbia University, 2 New York
State Psychiatric Institute, and 3 Howard Hughes Medical
Institute, New York, New York 10032
We have begun to analyze several elementary forms of learning in a
simple preparation consisting of the isolated mantle organs and
abdominal ganglion of Aplysia. Previous studies
suggested that plasticity at siphon sensory neuron synapses contributes to habituation and dishabituation of the gill- and siphon-withdrawal reflex in this preparation. We next wished to identify the sensory neurons that participate in the reflex and examine their plasticity more directly. To investigate the contribution of the LE siphon mechanosensory cells, we recorded from them and gill or siphon motor
neurons during the same siphon stimulation that has been used in
behavioral experiments in this preparation. Our results indicate that
the LE cells make a substantial contribution to the evoked response in
the motor neurons under these conditions, but they suggest that other
as yet unidentified siphon sensory neurons with lower thresholds and
shorter latencies also contribute. In addition, we find that
homosynaptic depression of monosynaptic postsynaptic potentials (PSPs)
from LE sensory cells makes an important contribution to habituation of
the response in the motor neurons. To investigate plasticity of PSPs
from the unidentified sensory neurons, we recorded the PSP that was
produced in a motor neuron by water-movement stimulation of the siphon,
which does not cause firing of LE cells. Our results suggest that PSPs
from the unidentified sensory neurons and the LE neurons undergo
similar plasticity during habituation and dishabituation training.
These results support the idea that plasticity at synapses of both LE and unidentified sensory neurons contributes to habituation and dishabituation of the reflex response in this preparation.
Key words:
Aplysia;
gill-withdrawal reflex;
siphon;
sensory neurons;
latency;
threshold;
habituation;
dishabituation;
learning
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