Characterization of 4 light-responsive putative motor neurons in the pedal ganglia ofHermissenda crassicornis

As part of the analysis of the circuitry underlying phototaxis, 4 light-responsive pedal neurons were identified and characterized. The 4 newly identified neurons have been designated as pedal neurons P7, P8, P9 and P10. Pedal cell P7 has an inhibitory response to light, lasting several minutes. Pedal cells P8, P9 and P10 exhibit excitatory 'on' responses to light that last for a few seconds after light onset. Lucifer yellow fills showed that each identified pedal cell has only one process which exits the nervous system through one of the pedal nerves. Various procedures were used to investigate the responses to illumination expressed by the 4 identified pedal neurons. The results indicate that: (1) the light responses are not intrinsic, but are due to synaptic input from other light-responsive cell(s), and (2) the sources of the synaptic input to the pedal cells are the photoreceptors of the eye, and not extraocular photoreceptors or light sensitive neurons within the circumesophageal nervous system.

[1]  T. Crow,et al.  Conditioned modification of phototactic behavior in Hermissenda. II. Differential adaptation of B-photoreceptors , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[2]  J. Farley,et al.  Motor correlates of phototaxis and associative learning in Hermissenda crassicornis , 1987, Brain Research Bulletin.

[3]  D. Alkon,et al.  Ocular and extraocular responses of identifiable neurons in pedal ganglia of Hermissenda crassicornis. , 1981, Journal of neurophysiology.

[4]  G. Block,et al.  Cerebral photoreceptors in Aplysia , 1973 .

[5]  Daniel L. Alkon,et al.  Responses of Photoreceptors in Hermissenda , 1972, The Journal of general physiology.

[6]  Intersensory Interactions in Hermissenda , 1973, The Journal of general physiology.

[7]  A. Brown,et al.  Light Response of a Giant Aplysia Neuron , 1973, The Journal of general physiology.

[8]  D L Alkon,et al.  Sensory convergence on central visual neurons in Hermissenda. , 1980, Journal of neurophysiology.

[9]  T. Crow,et al.  Light paired with serotonin in vivo produces both short- and long-term enhancement of generator potentials of identified B-photoreceptors in Hermissenda , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[10]  D. L. Alkon,et al.  Membrane depolarization accumulates during acquisition of an associative behavioral change. , 1980, Science.

[11]  T. Crow,et al.  Retention of an associative behavioral change in Hermissenda. , 1978, Science.

[12]  D. Alkon,et al.  Neural Organization of a Molluscan Visual System , 1973, The Journal of general physiology.

[13]  G. Hoyle,et al.  Neural events underlying learning in insects: changes in pacemaker , 1977, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[14]  D. Alkon,et al.  Hair Cell Generator Potentials , 1973, The Journal of general physiology.

[15]  D. Cook,et al.  Operant conditioning of head-waving in Aplysia. III. Cellular analysis of possible reinforcement pathways , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  D L Alkon,et al.  Sensory, interneuronal, and motor interactions within Hermissenda visual pathway. , 1984, Journal of neurophysiology.

[17]  D. Alkon Responses of hair cells to statocyst rotation , 1975, The Journal of general physiology.

[18]  D L Alkon,et al.  Ultrastructure of photoreceptors in the eye ofHermissenda labelled with intracellular injections of horseradish peroxidase , 1979, Journal of neurocytology.

[19]  D. Alkon,et al.  Associative Behavioral Modification in Hermissenda: Cellular Correlates , 1980, Science.

[20]  D. Alkon,et al.  Input and output changes of an identified neural pathway are correlated with associative learning in Hermissenda , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.