Neural Organization of the Median Ocellus of the Dragonfly

Intracellular responses from receptors and postsynaptic units have been recorded in the median ocellus of the dragonfly. The receptors respond to light with a graded, depolarizing potential and a single, tetrodotoxin-sensitive impulse at "on." The postsynaptic units (ocellar nerve dendrites) hyperpolarize during illumination and show a transient, depolarizing response at "off." The light-evoked slow potential responses of the postsynaptic units are not altered by the application of tetrodotoxin to the ocellus. It appears, therefore, that the graded receptor potential, which survives the application of tetrodotoxin, is responsible for mediating synaptic transmission in the ocellus. Comparison of pre- and postsynaptic slow potential activity shows (a) longer latencies in postsynaptic units by 5–20 msec, (b) enhanced photosensitivity in postsynaptic units by 1–2 log units, and (c) more transient responses in postsynaptic units. It is suggested that enhanced photosensitivity of postsynaptic activity is a result of summation of many receptors onto the postsynaptic elements, and that transients in the postsynaptic responses are related to the complex synaptic arrangements in the ocellar plexus to be described in the following paper.

[1]  J. Dowling,et al.  Neural Organization of the Median Ocellus of the Dragonfly , 1972, The Journal of general physiology.

[2]  R. Devoe Dual Sensitivities of Cells in Wolf Spider Eyes at Ultraviolet and Visible Wavelengths of Light , 1972, The Journal of general physiology.

[3]  D. Arnett Receptive Field Organization of Units in the First Optic Ganglion of Diptera , 1971, Science.

[4]  W. Pak,et al.  On-Transient of Insect Electroretinogram: Its Cellular Origin , 1971, Science.

[5]  A. Gorman,et al.  Photoreceptor Potentials of Opposite Polarity in the Eye of the Scallop, Pecten irradians , 1970, The Journal of general physiology.

[6]  J. Dowling,et al.  Intracellular responses of the Müller (glial) cells of mudpuppy retina: their relation to b-wave of the electroretinogram. , 1970, Journal of neurophysiology.

[7]  A. Kaneko Physiological and morphological identification of horizontal, bipolar and amacrine cells in goldfish retina , 1970, The Journal of physiology.

[8]  J. Dowling,et al.  Organization of retina of the mudpuppy, Necturus maculosus. I. Synaptic structure. , 1969, Journal of neurophysiology.

[9]  J. Dowling,et al.  Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording. , 1969, Journal of neurophysiology.

[10]  A. Perrelet,et al.  EVIDENCE FOR EXTRACELLULAR SPACE IN THE RHABDOME OF THE HONEYBEE DRONE EYE , 1969, The Journal of cell biology.

[11]  F. Baumann Slow and Spike Potentials Recorded from Retinula Cells of the Honeybee Drone in Response to Light , 1968, The Journal of general physiology.

[12]  T. Goldsmith,et al.  Propertiesof intact photoreceptor cells lacking synapses. , 1968, The Journal of experimental zoology.

[13]  R. Llinás,et al.  Transmitter Release at the Squid Giant Synapse in the Presence of Tetrodotoxin , 1966, Nature.

[14]  G. Gwilliam,et al.  THE MECHANISM OF THE SHADOW REFLEX IN CIRRIPEDIA. II. PHOTORECEPTOR CELL RESPONSE, SECOND-ORDER RESPONSES, AND MOTOR CELL OUTPUT , 1965 .

[15]  B. Katz,et al.  Release of Acetylcholine from a Nerve Terminal by Electric Pulses of Variable Strength and Duration , 1965, Nature.

[16]  D. Elmqvist,et al.  Spontaneous activity at a mammalian neuromuscular junction in tetrodotoxin. , 1965, Acta physiologica Scandinavica.

[17]  P. Ruck,et al.  The structure of the insect dorsal ocellus. I. General organization of the ocellus in dragonflies , 1964 .

[18]  J. Scholes,et al.  Discrete Subthreshold Potentials from the Dimly Lit Insect Eye , 1964, Nature.

[19]  G. Gwilliam,et al.  THE MECHANISM OF THE SHADOW REFLEX IN CIRRIPEDIA. I. ELECTRICAL ACTIVITY IN THE SUPRAESOPHAGEAL GANGLION AND OCELLAR NERVE , 1963 .

[20]  C. Terzuolo,et al.  Separation of Transducer and Impulse-Generating Processes in Sensory Receptors , 1963, Science.

[21]  M. Fuortes,et al.  Visual Responses in the Eye of the Dragon Fly , 1963, Science.

[22]  K. Naka,et al.  Spike Potentials Recorded from the Insect Photoreceptor , 1962, The Journal of general physiology.

[23]  H. Autrum,et al.  Beziehungen zwischen Lichtreiz und Erregung im Ocellusnerven von Calliphora erythrocephala , 1961 .

[24]  K. Naka,et al.  Recording of Retinal Action Potentials from Single Cells in the Insect Compound Eye , 1961, The Journal of general physiology.

[25]  P. Ruck Electrophysiology of the Insect Dorsal Ocellus , 1961, The Journal of general physiology.

[26]  E. MacNichol,et al.  Electrical Responses of the Retinal Nerve and Optic Ganglion of the Squid , 1960, Science.

[27]  H. Autrum,et al.  Die Belichtungspotentiale einzelner Sehzellen von Calliphora erythrocephala Meig , 1960 .

[28]  T. Furukawa,et al.  Effects of tetrodotoxin on the neuromuscular junction. , 1959, The Japanese journal of physiology.

[29]  G. Hoyle Functioning of the Insect Ocellar Nerve , 1955 .

[30]  P. Ruck Electrical responses of insect dorsal ocelli. , 1954, Journal of cellular and comparative physiology.

[31]  D. Parry The function of the insect ocellus. , 1947, The Journal of experimental biology.

[32]  J. Eccles,et al.  An Electrical Hypothesis of Central Inhibition , 1947, Nature.

[33]  M. Murakami,et al.  Duality of conduction mechanism in bipolar cells of the frog retina. , 1970, Vision research.

[34]  J. Scholes,et al.  Discontinuity of the excitation process in locust visual cells. , 1965, Cold Spring Harbor symposia on quantitative biology.

[35]  J. Eccles The Physiology of Synapses , 1964, Springer Berlin Heidelberg.

[36]  P. Ruck The electrical responses of dorsal ocelli in cockroaches and grasshoppers , 1957 .

[37]  L. Mullins,et al.  Molecular structure and functional activity of nerve cells , 1956 .