Dynamic relationship between the slow potential and spikes in cockroach ocellar neurons
- PMID: 3418318
- PMCID: PMC2216152
- DOI: 10.1085/jgp.91.5.703
Dynamic relationship between the slow potential and spikes in cockroach ocellar neurons
Abstract
The relationship between the slow potential and spikes of second-order ocellar neurons of the cockroach, Periplaneta americana, was studied. The stimulus was a sinusoidally modulated light with various mean illuminances. A solitary spike was generated at the depolarizing phase of the modulation response. Analysis of the relationship between the amplitude/frequency of voltage modulation and the rate of spike generation showed that (a) the spike initiation process was bandpass at approximately 0.5-5 Hz, (b) the process contained a dynamic linearity and a static nonlinearity, and (c) the spike threshold at optimal frequencies (0.5-5 Hz) remained unchanged over a mean illuminance range of 3.6 log units, whereas (d) the spike threshold at frequencies of less than 0.5 Hz was lower at a dimmer mean illuminance. The voltage noise in the response was larger and the mean membrane potential level was more positive at a dimmer mean illuminance. Steady or noise current injection during sinusoidal light stimulation showed that (a) the decrease in the spike threshold at a dimmer mean illuminance was due to the increase in the noise variance: the noise had facilitatory effects on the spike initiation; and (b) the change in the mean potential level had little effect on the spike threshold. We conclude that fundamental signal modifications occur during the spike initiation in the cockroach ocellar neuron, a finding that differs from the spike initiation process in other visual systems, including Limulus eye and vertebrate retina, in which it is presumed that little signal modification occurs at the analog-to-digital conversion process.
Similar articles
-
Nonlinear signal transmission between second- and third-order neurons of cockroach ocelli.J Gen Physiol. 1990 Feb;95(2):297-317. doi: 10.1085/jgp.95.2.297. J Gen Physiol. 1990. PMID: 2155282 Free PMC article.
-
Dynamics of cockroach ocellar neurons.J Gen Physiol. 1986 Aug;88(2):275-92. doi: 10.1085/jgp.88.2.275. J Gen Physiol. 1986. PMID: 3746252 Free PMC article.
-
Morphological and physiological characterization of descending ocellar interneurons in the American cockroach.J Comp Neurol. 1990 Nov 22;301(4):511-9. doi: 10.1002/cne.903010403. J Comp Neurol. 1990. PMID: 2273097
-
Morphological and physiological characterization of small multimodal ocellar interneurons in the American cockroach.J Comp Neurol. 1990 Nov 22;301(4):501-10. doi: 10.1002/cne.903010402. J Comp Neurol. 1990. PMID: 2273096
-
Functional diversity of neural organization in insect ocellar systems.Vision Res. 1995 Feb;35(4):443-52. doi: 10.1016/0042-6989(94)00192-o. Vision Res. 1995. PMID: 7900285 Review.
Cited by
-
Gain control of synaptic transfer from second- to third-order neurons of cockroach ocelli.J Gen Physiol. 1996 Jan;107(1):121-31. doi: 10.1085/jgp.107.1.121. J Gen Physiol. 1996. PMID: 8741734 Free PMC article.
-
Spikes in retinal bipolar cells phase-lock to visual stimuli with millisecond precision.Curr Biol. 2011 Nov 22;21(22):1859-69. doi: 10.1016/j.cub.2011.09.042. Epub 2011 Nov 3. Curr Biol. 2011. PMID: 22055291 Free PMC article.
-
Nonlinear signal transmission between second- and third-order neurons of cockroach ocelli.J Gen Physiol. 1990 Feb;95(2):297-317. doi: 10.1085/jgp.95.2.297. J Gen Physiol. 1990. PMID: 2155282 Free PMC article.
-
Pavlov's cockroach: classical conditioning of salivation in an insect.PLoS One. 2007 Jun 13;2(6):e529. doi: 10.1371/journal.pone.0000529. PLoS One. 2007. PMID: 17565382 Free PMC article.
-
White noise analysis of graded response in a wind-sensitive, nonspiking interneuron of the cockroach.J Comp Physiol A. 1991 Apr;168(4):429-43. doi: 10.1007/BF00199603. J Comp Physiol A. 1991. PMID: 1713969