Browse > Article
http://dx.doi.org/10.4196/kjpp.2011.15.6.371

A Computational Model of the Temperature-dependent Changes in Firing Patterns in Aplysia Neurons  

Hyun, Nam-Gyu (Department of Physics, Jeju National University)
Hyun, Kwang-Ho (Department of Biological Sciences, Korea Advanced Institute of Science and Technology)
Hyun, Kwang-Beom (Department of Biological Sciences, Korea Advanced Institute of Science and Technology)
Han, Jin-Hee (Department of Biological Sciences, KAIST Institute for the Bio Century (KIB))
Lee, Kyung-Min (Department of Anatomy, Graduate School of Medicine, Kyungpook National University)
Kaang, Bong-Kiun (National Creative Research Initiative Center for Memory, Departments of Biological Sciences and Brain and Cognitive Sciences, College of Natural Science, Seoul National University)
Publication Information
The Korean Journal of Physiology and Pharmacology / v.15, no.6, 2011 , pp. 371-382 More about this Journal
Abstract
We performed experiments using Aplysia neurons to identify the mechanism underlying the changes in the firing patterns in response to temperature changes. When the temperature was gradually increased from $11^{\circ}C$ to $31^{\circ}C$ the firing patterns changed sequentially from the silent state to beating, doublets, beating-chaos, bursting-chaos, square-wave bursting, and bursting-oscillation patterns. When the temperature was decreased over the same temperature range, these sequential changes in the firing patterns reappeared in reverse order. To simulate this entire range of spiking patterns we modified nonlinear differential equations that Chay and Lee made using temperature-dependent scaling factors. To refine the equations, we also analyzed the spike pattern changes in the presence of potassium channel blockers. Based on the solutions of these equations and potassium channel blocker experiments, we found that, as temperature increases, the maximum value of the potassium channel relaxation time constant, ${\tau}_n(t)$ increases, but the maximum value of the probabilities of openings for activation of the potassium channels, n(t) decreases. Accordingly, the voltage-dependent potassium current is likely to play a leading role in the temperature-dependent changes in the firing patterns in Aplysia neurons.
Keywords
Aplysia; Bursting; Doublet; Temperature-dependent scaling factor; Computer simulation;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
Times Cited By Web Of Science : 2  (Related Records In Web of Science)
Times Cited By SCOPUS : 2
연도 인용수 순위
1 Braun HA, Huber MT, Dewald M, Schafer K, Voigt K. Computer simulations of neuronal signal transduction: the role of nonlinear dynamics and noise. Int J Bifurcation Chaos. 1998;8:881-889.   DOI   ScienceOn
2 Finke C, Freund JA, Rosa E Jr, Braun HA, Feudel U. On the role of subthreshold currents in the Huber-Braun cold receptor model. Chaos. 2010;20:045107.   DOI   ScienceOn
3 Lim CS, Chung DY, Kaang BK. Partial anatomical and physiological characterization and dissociated cell culture of the nervous system of the marine mollusc Aplysia kurodai. Mol Cells. 1997;7:399-407.
4 Hyun NG, Hyun KH, Lee K, Kaang BK. Temperature Dependence of Action Potential Parameters in Aplysia Neurons. Neurosignals. 2011 (in press).
5 Hille B. Ion channels of excitable membranes. 3rd ed. Sunderland Mass: Sinauer; 2001. 366 p.
6 Hyun NG. The brain and the mind. 1st ed. Jeju: Jeju Nat Univ; 2007. 321-338 p.
7 Wang LY, Fedchyshyn MJ, Yang YM. Action potential evoked transmitter release in central synapses: insights from the developing calyx of Held. Mol Brain. 2009;2:36.   DOI
8 Volk KA, Matsuda JJ, Shibata EF. A voltage-dependent potassium current in rabbit coronary artery smooth muscle cells. J Physiol. 1991;439:751-768.
9 Spruce AE, Standen NB, Stanfield PR. The action of external tetraethylammonium ions on unitary delayed rectifier potassium channels of frog skeletal muscle. J Physiol. 1987;393:467-478.
10 Carpenter DO. Temperature effects on pacemaker generation, membrane potential, and critical firing threshold in Aplysia neurons. J Gen Physiol. 1967;50:1469-1484.   DOI   ScienceOn
11 Moffett S, Wachtel H. Correlations between temperature effects on behavior in Aplysia and firing patterns of identified neurons. Mar Behav Physiol. 1976;4:61-74.   DOI   ScienceOn
12 Carpenter DO, Alving BO. A contribution of an electrogenic $Na^+$ pump to membrane potential in Aplysia neurons. J Gen Physiol. 1968;52:1-21.   DOI   ScienceOn
13 Fletcher SD, Ram JL. High temperature induces reversible silence in Aplysia R15 bursting pacemaker neuron. Comp Biochem Physiol. 1991;98A:399-405.
14 Hakozaki S, Matsumoto M, Sasaki K. Temperature-sensitive activation of G-protein regulating the resting membrane conductance of Aplysia neurons. Jpn J Physiol. 1989;39:115-130.   DOI   ScienceOn
15 Chay TR. Bursting excitable cell models by a slow $Ca^{2+}$ current. J Theor Biol. 1990;142:305-315.   DOI   ScienceOn
16 Schafer K, Braun HA, Kurten L. Analysis of cold and warm receptor activity in vampire bats and mice. Pflugers Arch. 1988;412:188-194.
17 Chay TR, Lee YS. Bursting, beating, and chaos by two functionally distinct inward current inactivations in excitable cells. Ann N Y Acad Sci. 1990;591:328-350.   DOI
18 Hensel H, Huopaniemi T. Static and dynamic properties of warm fibres in the infraorbital nerve. Pflugers Arch. 1969;309:1-10.   DOI   ScienceOn
19 Hensel H, Schafer K. Static an dynamic activity of cold receptors in cats after long-term exposure to various temperatures. Pflugers Arch. 1982;392:291-294.   DOI   ScienceOn
20 Hensel H. Static and dynamic activity of warm receptors in Boa constrictor. Pflugers Arch. 1975;353:191-199.   DOI   ScienceOn
21 Kim YD, Cho MH, Kwon SC. Myoplasmic [$Ca^{2+}$], crossbridge phosphorylation and latch in rabbit bladder smooth muscle. Korean J Physiol Pharmacol. 2011;15:171-177.   DOI
22 Kim KS, Shin DH, Nam JH, Park KS, Zhang YH, Kim WK, Kim SJ. Functional expression of TRPV4 cation channels in human mast cell line (HMC-1). Korean J Physiol Pharmacol. 2010;14:419-425.   DOI