ArticleBiophysical journal1993
Reconstruction of ionic currents in a molluscan photoreceptor.
Article in Biophysical journal, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed, 22 citations in OpenAlex.
- Subcellular, cellular, and circuit mechanisms underlying classical conditioning in Hermissenda crassicornis.Anatomical record. Part B, New anatomist · 2006Review
- Inhibition of conditioned stimulus pathway phosphoprotein 24 expression blocks the reduction in A-type transient K+ current produced by one-trial in vitro conditioning of Hermissenda.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005Article
- Comparison of Hermissenda type a and type B photoreceptors: response to light as a function of intensity and duration.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2003Article
- The effect of intensity and duration on the light-induced sodium and potassium currents in the Hermissenda type B photoreceptor.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002Article
- Modeling Hermissenda: II. Effects of variations in type-B cell excitability, synaptic strength, and network architecture.Journal of computational neuroscience · 1996Article
- Modeling Hermissenda: I. Differential contributions of IA and IC to type-B cell plasticity.Journal of computational neuroscience · 1996Article
- Associative learning in a network model of Hermissenda crassicornis. I. Theory.Biological cybernetics · 1992Article
- Computational study of enhanced excitability in Hermissenda: membrane conductances modulated by 5-HT.Journal of computational neuroscienceArticle
- Evidence for a distinct light-induced calcium-dependent potassium current in Hermissenda crassicornis.Journal of computational neuroscienceArticle
- Paired turbulence and light do not produce a supralinear calcium increase in Hermissenda.Journal of computational neuroscienceArticle
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5 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
Two-microelectrode voltage-clamp measurements were made to determine the kinetics and voltage dependence of ionic currents across the soma membrane of the Hermissenda type B photoreceptor. The voltage-dependent outward potassium currents, IA and ICa(2+)-K+, the inward voltage-dependent calcium current, ICa2+ and the light-induced current, IIgt, were then described with Hodgkin-Huxley-type equations. The fast-activating and inactivating potassium current, IA, was described by the equation; IA(t) = gA(max)(ma infinity[1-exp(-t/tau ma)])3 x (ha infinity [1-exp(-t/tau ha)] + exp(-t/tau ha)) (Vm-EK), where the parameters ma infinity, ha infinity, tau ma, and tau ha are functions of membrane potential, Vm, and ma infinity and ha infinity are steady-state activation and inactivation parameters. Similarly, the calcium-dependent outward potassium current, ICa(2+)-K+, was described by the equation, ICa(2+)-K+ (t) = gc(max)(mc infinity(VC)(1-exp[-t/tau mc (VC)]))pc (hc infinity(VC) [1-exp(-t/tau hc)] + exp(-t/tau hc(VC)])pc(VC-EK). In high external potassium, ICa(2+)-K+ could be measured in approximate isolation from other currents as a voltage-dependent inward tail current following a depolarizing command pulse from a holding potential of -60 mV. A voltage-dependent inward calcium current across the type B soma membrane, ICa2+, activated rapidly, showed little inactivation, and was described by the equation: ICa2+ = gCa(max) [1 + exp](-Vm-5)/7]-1 (Vm-ECa), where gCa(max) was 0.5 microS. The light-induced current with both fast and slow phases was described by: IIgt(t) = IIgt1 + IIgt2 + IIgt3, IIgti = gIgti [1-exp(- ton/tau mi)] exp(-ton/tau hi)(Vm-EIgti) (i = 1, 2). For i = 3, /Igt(t) = gigt3m33h3(Vm - Eigt3)exp(-ton/Ton) x exp(-tfoff/t Off). Based on these reconstructions of ionic currents, learning-induced enhancement of the long lasting depolarization (LLD) of the photoreceptor'slight response was shown to arise from progressive inactivation of /A, lca2+ -K+, and lCa2+.
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