Abstract
In these companion papers, we study how the interrelated dynamics of sodium and potassium affect the excitability of neurons, the occurrence of seizures, and the stability of persistent states of activity. In this first paper, we construct a mathematical model consisting of a single conductance-based neuron together with intra- and extracellular ion concentration dynamics. We formulate a reduction of this model that permits a detailed bifurcation analysis, and show that the reduced model is a reasonable approximation of the full model. We find that competition between intrinsic neuronal currents, sodium-potassium pumps, glia, and diffusion can produce very slow and large-amplitude oscillations in ion concentrations similar to what is seen physiologically in seizures. Using the reduced model, we identify the dynamical mechanisms that give rise to these phenomena. These models reveal several experimentally testable predictions. Our work emphasizes the critical role of ion concentration homeostasis in the proper functioning of neurons, and points to important fundamental processes that may underlie pathological states such as epilepsy.
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Notes
Depending on the stability of the periodic orbit involved, Hopf bifurcations are classified as sub- or supercritical.
The stable and unstable periodic orbits involved in this scenario appear via a saddle-node bifurcation at a slightly smaller parameter value that is extremely close to that of the Hopf bifurcation. Thus, the sequence of bifurcations is not immediately apparent in Fig. 2. The abruptness of these transitions, and the difficulty in resolving them numerically, is due to the “canard” mechanism (Dumortier and Roussarie 1996; Wechselberger (2007)).
A canard similar to that described previously occurs here, so that the Hopf and the saddle-node bifurcations on the left sides of Figs. 3a and b occur in extremely narrow intervals of the parameter.
In Fig. 3a, the equilibrium curve does not extend all the way to zero because of the constant chloride leak current.
Note that oscillations may persist slightly outside of the RO, where a stable periodic orbit coexists with the stable equilibrium solution; see, for example, the right side of Fig. 3a.
References
Amzica, F., Massimini, M., & Manfridi, A. (2002). A spatial buffering during slow and paroxysmal sleep oscillations in cortical networks of glial cells in vivo. The Journal of Neuroscience, 22, 1042–1053.
Bazhenov, M., Timofeev, I., Steriade, M., & Sejnowski, T. J. (2004). Potassium model for slow (2-3 Hz) in vivo neocortical paroxysmal oscillations. Journal of Neurophysiology, 92, 1116–1132. doi:10.1152/jn.00529.2003.
Bikson, M., Hahn, P. J., Fox, J. E., & Jefferys, J. G. R. (2003). Depolarization block of neurons during maintenance of electrographic seizures. Journal of Neurophysiology, 90(4), 2402–2408. doi:10.1152/jn.00467.2003.
Cressman, J. R., Ullah, G., Ziburkus, J., Schiff, S. J., & Barreto, E. (2008). Ion concentration dynamics: mechanisms for bursting and seizing. BMC Neuroscience, 9(Suppl 1), O9. doi:10.1186/1471-2202-9-S1-O9.
Dumortier, F., & Roussarie, R. (1996). Canard cycles and center manifolds. Memoirs of the American Mathematical Society, 121(577), 1–100.
Ermentrout, G. B. (2002). Simulating, Analyzing, and Animating Dynamical Systems: A Guide to XPPAUT for Researchers and Students. Philadelphia: Society for Industrial and Applied Mathematics.
Feng, Z., & Durand, D. M. (2006). Effects of potassium concentration on firing patterns of low-calcium epileptiform activity in anesthetized rat hippocampus: inducing of persistent spike activity. Epilepsia, 47(4), 727–736. doi:10.1111/j.1528-1167.2006.00499.x.
Fisher, R. S., Pedley, T. A., & Prince, D. A. (1976). Kinetics of potassium movement in norman cortex. Brain Research, 101(2), 223–237. doi:10.1016/0006-8993(76)90265-1.
Frankenhaeuser, B., & Hodgkin, A. L. (1956). The after-effects of impulses in the giant nerve fibers of loligo. The Journal of Physiology, 131, 341–376.
Frohlich, F., Timofeev, I., Sejnowski, T. J., & Bazhenov, M. (2008). Extracellular potassium dynamics and epileptogenesis. In: I. Soltesz, & K. Staley (eds.), Computational Neuroscience in Epilepsy (p. 419).
Gluckman, B. J., Nguyen, H., Weinstein, S. L., & Schiff, S. J. (2001). Adaptive electric field control of epileptic seizures. The Journal of Neuroscience, 21(2), 590–600.
Heinemann, U., Lux, H. D., & Gutnick, M. J. (1977). Extracellular free calcium and potassium during paroxysmal activity in the cerebral cortex of the cat. Experimental Brain Research, 27, 237–243. doi:10.1007/BF00235500.
Hodgkin, A. L., & Huxley, A. F. (1952). A quantitative description of membrane current and its application to conduction and excitation in nerve. The Journal of Physiology, 117, 500–544.
Jensen, M. S., & Yaari, Y. (1997). Role of intrinsic burs firing, potassium accumulation, and electrical coupling in the elevated potassium model of hippocampal epilepsy. Journal of Neurophysiology, 77, 1224–1233.
Kager, H., Wadman, W. J., & Somjen, G. G. (2000). Simulated seizures and spreading depression in a neuron model incorporating interstitial space and ion concentrations. Journal of Neurophysiology, 84, 495–512.
Kager, H., Wadman, W. J., & Somjen, G. G. (2007). Seizure-like after discharges simulated in a model neuron. Journal of Computational Neuroscience, 22, 105–108. doi:10.1007/s10827-006-0001-y.
Kepler, T. B., Abbott, L. F., & Mardner, E. (1992). Reduction of conductance-based neuron models. Biological Cybernetics, 66, 381–387. doi:10.1007/BF00197717.
Kuschinsky, W., Wahl, M., Bosse, O., & Thurau, K. (1972). The dependency of the pial arterial and arteriolar resistance on the perivascular H+ and K+ conconcentrations. A micropuncture Study. European Neurology, 6(1), 92–5.
Lauger, P. (1991). Electrogenic ion pumps. Sunderland, MA: Sinauer.
Mason, A., & Larkman, A. (1990). Correlations between morphology and electrophysiology of pyramidal neurons in slices of rat visual cortex. II. Electrophysiology. The Journal of Neuroscience, 10(5), 1415–1428.
Mazel, T., Simonova, Z., & Sykova, E. (1998). Diffusion heterogeneity and anisotropy in rat hippocampus. Neuroreport, 9(7), 1299–1304. doi:10.1097/00001756-199805110-00008.
McBain, C. J. (1994). Hippocampal inhibitory neuron activity in the elevated potassium model of epilepsy. Journal of Neurophysiology, 72, 2853–2863.
McBain, C. J., Traynelis, S. F., & Dingledine, R. (1990). Regional variation of extracellular space in the hippocampus. Science, 249(4969), 674–677. doi:10.1126/science.2382142.
McCulloch, J., Edvinsson, L., & Watt P. (1982). Comparison of the effects of potassium and pH on the caliber of cerebral veins and arteries. Pflugers Archiv, 393(1), 95–8
Moody, W. J., Futamachi, K. J., & Prince, D. A. (1974). Extracellular potassium activity during epileptogenesis. Experimental Neurology, 42, 248–263. doi:10.1016/0014-4886(74)90023-5.
Park, E., & Durand, D. M. (2006). Role of potassium lateral diffusion in non-synaptic epilepsy: A computational study. Journal of Theoretical Biology, 238, 666–682. doi:10.1016/j.jtbi.2005.06.015.
Paulson, O. B., & Newman, E. A. (1987). Does the release of potassium from astrocyte endfeet regulate cerebral blood flow? Science, 237(4817), 896–898. doi:10.1126/science.3616619.
Pinsky, P. F., & Rinzel, J. (1994). Intrinsic and network rhythmogenesis in a reduced Traub model for CA3 neurons. Journal of Computational Neuroscience, 1, 39–60. doi:10.1007/BF00962717.
Ransom, C. B., Ransom, B. R., & Sotheimer, H. (2000). Activity-dependent extracellular K+ accumulation in rat optic nerve: the role of glial and axonal Na+ pumps. The Journal of Physiology, 522, 427–442. doi:10.1111/j.1469-7793.2000.00427.x.
Rinzel, J. (1985). Excitation dynamics: insights from simplified membrane models. Federation Proceedings, 44, 2944–2946.
Rinzel, J., & Ermentrout, B. (1989). Analysis of neuronal excitability and oscillations, in “Methods in neuronal modeling: From synapses to networks”, Koch, C., & Segev, I. MIT Press, revised (1998).
Rutecki, P. A., Lebeda, F. J., & Johnston, D. (1985). Epileptiform activity induced by changes in extracellular potassium in hippocampus. Journal of Neurophysiology, 54, 1363–1374.
Scharrer, E. (1944). The blood vessels of the nervous tissue. The Quarterly Review of Biology, 19(4), 308–318. doi:10.1086/394698.
Somjen, G. G. (2004). Ions in the Brain. New York: Oxford University Press.
Strogatz, S. H. (1994). Nonlinear Dynamics and Chaos. MA: Addison-Wesley, Reading.
Traynelis, S. F., & Dingledine, R. (1988). Potassium-induced spontaneous electrographic seizures in the rat hippocampal slice. Journal of Neurophysiology, 59, 259–276.
Ullah, G., Cressman, J. R., Barreto, E., & Schiff, S. J. (2009). The influence of sodium and potassium dynamics on excitability, seizures, and the stability of persistent states: II. Network and glial dynamics. Journal of Computational Neuroscience doi:10.1007/s10827-008-0130-6.
Wang, X. J. (1999). Synaptic basis of cortical persistent activity: the importance of NMDA receptors to working memory. The Journal of Neuroscience, 19(21), 9587–9603.
Wechselberger, M. (2007). Scholarpedia, 2(4), 1356.
Ziburkus, J., Cressman, J. R., Barreto, E., & Schiff, S. J. (2006). Interneuron and pyramidal cell interplay during in vitro seizure-like events. Journal of Neurophysiology, 95, 3948–3954. doi:10.1152/jn.01378.2005.
Acknowledgements
This work was funded by NIH Grants K02MH01493 (SJS), R01MH50006 (SJS, GU), F32NS051072 (JRC), and CRCNS-R01MH079502 (EB).
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Action Editor: Alain Destexhe
An erratum to this article is available at http://dx.doi.org/10.1007/s10827-011-0333-0.
Appendix
Appendix
1.1 Current to concentration conversion:
In order to derive the ion concentration dynamics, we begin with the assumption that the ratio of the intracellular volume to the extracellular volume is β = 7.0 (Somjen 2004). This corresponds to a cell with intracellular and extracellular space of 87.5% and 12.5% of the total volume respectively. For the currents across the membrane, conservation of ions requires
where c and Vol represent ion concentration and volume respectively, Δ indicates change, and the subscripts i, o correspond to the intra- and extracellular values. The above equation leads to
Let I be the current density in units of μA/cm2 from the Hodgkin–Huxley model. Then, the total current i total = IA entering the intracellular volume produces a flow of charge equal to ΔQ = i totalΔt in a time Δt, where A is the membrane area. The number of ions entering the volume in this time is therefore ΔN = i totalΔt/q where q is 1.6 × 10−19 coul. The change in concentration Δc i = ΔN/N A Vol i depends on the volume of the region to which the ions flow, where Avogadro’s number N A converts the concentration to molars. The rate of change of concentration, or concentration current dc i/dt = i c,i, is related to the ratio of the surface area of the cell to the volume of the cell as follows
For a sphere of radius 7 μm, α = 21 mcoul/M cm2. An increase in cell volume would result in a smaller time constant and therefore slower dynamics.
For the outward current the external ion concentration is therefore given as
1.2 Equations for reduced model:
The reduced model uses empirical fits of the average membrane currents of the Hodgkin-Huxley model neuron, as described in the main text. The fits are given below.
where
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Cressman, J.R., Ullah, G., Ziburkus, J. et al. The influence of sodium and potassium dynamics on excitability, seizures, and the stability of persistent states: I. Single neuron dynamics. J Comput Neurosci 26, 159–170 (2009). https://doi.org/10.1007/s10827-008-0132-4
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DOI: https://doi.org/10.1007/s10827-008-0132-4