Gain control of synaptic transfer from second- to third-order neurons of cockroach ocelli.
Open Access
- 1 January 1996
- journal article
- research article
- Published by Rockefeller University Press in The Journal of general physiology
- Vol. 107 (1) , 121-131
- https://doi.org/10.1085/jgp.107.1.121
Abstract
Synaptic transmission from second- to third-order neurons of cockroach ocelli occurs in an exponentially rising part of the overall sigmoidal characteristic curve relating pre- and postsynaptic voltage. Because of the nonlinear nature of the synapse, linear responses of second-order neurons to changes in ligh intensity are half-wave rectified, i.e., the response to a decrement in light is amplified whereas that to an increment in light is compressed. Here I report that the gain of synaptic transmission from second- to third-order neurons changes by ambient light levels and by wind stimulation applied to the cerci. Transfer characteristics of the synapse were studied by simultaneous intracellular recordings of second- and third-order neurons. Potential changes were evoked in second-order neurons by a sinusoidally modulated light with various mean luminances. With a decrease in the mean luminance (a) the mean membrane potential of second-order neurons was depolarized, (b) the synapse between the second- and third-order neurons operated in a steeper range of the exponential characteristic curve, where the gain to transmit modulatory signals was higher, and (c) the gain of third-order neurons to detect a decrement in light increased. Second-order neurons were depolarized when a wind or tactile stimulus was applied to various parts of the body including the cerci. During a wind-evoked depolarization, the synapse operated in a steeper range of the characteristic curve, which resulted in an increased gain of third-order neurons to detect light decrements. I conclude that the nonlinear nature of the synapse between the second- and third-order neurons provides an opportunity for an adjustment of gain to transmit signals of intensity change. The possibility that a similar gain control occurs in other visual systems and underlies a more advanced visual function, i.e., detection of motion, is discussed.Keywords
This publication has 26 references indexed in Scilit:
- Neural organization of ocellar pathways in the cockroach brainJournal of Comparative Neurology, 1995
- Contrast gain, signal-to-noise ratio, and linearity in light-adapted blowfly photoreceptors.The Journal of general physiology, 1994
- Mechanisms of early visual processing in the medulla of the locust optic lobe: How self-inhibition, spatial-pooling, and signal rectification contribute to the properties of transient cellsVisual Neuroscience, 1991
- Morphological and physiological characterization of small multimodal ocellar interneurons in the American cockroachJournal of Comparative Neurology, 1990
- Nonlinear signal transmission between second- and third-order neurons of cockroach ocelli.The Journal of general physiology, 1990
- Dynamic relationship between the slow potential and spikes in cockroach ocellar neurons.The Journal of general physiology, 1988
- Dynamics of cockroach ocellar neurons.The Journal of general physiology, 1986
- Spatial and temporal properties of luminosity horizontal cells in the turtle retina.The Journal of general physiology, 1983
- Neuronal properties underlying processing of visual information in the barnacleNature, 1978
- Neural Organization of the Median Ocellus of the DragonflyThe Journal of general physiology, 1972