| Surface Charge of Giant Axons of Squid and Lobster Biophysical Journal, Volume 8, Issue 4, 1 April 1968, Pages 470-489 John R. Segal Abstract A method is described for the determination of the electrophoretic mobility of single, isolated, intact, giant axons of squid and lobster. In normal physiological solutions, the surface of hydrodynamic shear of these axons is negatively charged. The of the estimated surface charge density is -1.9×10 coul cm for squid axons, -4.2×10 coul cm for lobster axons. The electrophoretic mobility of squid axons decreases greatly when the applied transaxial electric field is made sufficiently intense; action potential propagation is blocked irreversibly by transaxial electric fields of the same intensity. The squid axon recovers its mobility hours later and is then less affected by transaxial fields. Eventually, a state is reached in which the transaxial field irreversibly reverses the sign of the surface charge. In contrast, there is no obvious effect of electric field on the mobility of lobster axons. The mobility of lobster axons becomes undetectable in the presence of Th at a concentration which blocks the action potential, and in the presence of La at a concentration which does not affect propagation. Quinine does not alter lobster axon mobility at a concentration which blocks action potential conduction. Replacement of extracellular Na by K is without effect upon lobster axon mobility. The electrophysiological implications of the results are discussed. Abstract | PDF (1252 kb) |
| Cross-Polarized Reflected Light Measurement of Fast Optical Responses Associated with Neural Activation Biophysical Journal, Volume 88, Issue 6, 1 June 2005, Pages 4170-4177 Xin-Cheng Yao, Amanda Foust, David M. Rector, Benjamin Barrowes and John S. George Abstract We developed an optical probe for cross-polarized reflected light measurements and investigated optical signals associated with electrophysiological activation in isolated lobster nerves. The cross-polarized baseline light intensity (structural signal) and the amplitude of the transient response to stimulation (functional signal) measured in reflected mode were dependent on the orientation of the nerve axis relative to the polarization plane of incident light. The maximum structural signal and functional response amplitude were observed at 45°, and the ratio of functional to structural signals was approximately constant across orientations. Functional responses were measured in single trials in both transmitted and reflected geometries and responses had similar waveforms. Both structural and functional signals were an order of magnitude smaller in reflected than in transmitted light measurements, but functional responses had similar signal/noise ratios. We propose a theoretical model based on geometrical optics that is consistent with experimental results. In the model, the cross-polarized structural signal results from light reflection from axonal fibers and the transient functional response arises from axonal swelling associated with neural activation. Polarization-sensitive reflected light measurements could greatly enhance in vivo imaging of neural activation since cross-polarized responses are much larger than scattering signals now employed for dynamic functional neuroimaging. Abstract | Full Text | PDF (231 kb) |
| Saving endangered whales at no cost Current Biology, Volume 17, Issue 1, 9 January 2007, Pages R10-R11 Ransom A. Myers, Stephanie A. Boudreau, Robert D. Kenney, Michael J. Moore, Andrew A. Rosenberg, Scott A. Sherrill-Mix and Boris Worm Full Text | PDF (340 kb) |
Copyright © 1976 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 16, Issue 2, 121-136, 1 February 1976
doi:10.1016/S0006-3495(76)85669-X
Research Article
J.R. Clay and M.F. Shlesinger
A model is presented for the ionic mechanism of low frequency 1/f electrical noise which has been observed in axonal membranes. The model consists of narrow channels which open randomly throughout the membrane and remain open for only a short time compared with f-1max where fmax approximately 2 kHz is the maximum frequency for which 1/f noise is observed. The fluctuation in channel formation is coupled to low frequency normal mode vibrations in liquid crystals which have properties similar to nerve membranes. Ionic current flow through the channels is assumed to occur via single file diffusion. The diffusion process is regarded as a non-Markovian random walk on a one-dimensional lattice which is mathematically decomposed into its spatial and temporal components. This technique allows calculation of the mean and variance of the number of ions which flow through any single short-lived channel. The final result for the current noise power spectrum, S, is S(f) = (A + k/I/2)/f, where I is the mean membrane current and A and k are parameters which are independent of membrane voltage. The theoretical result is consistent with observations of 1/f noise in lobster axon by Poussart (1971, Biophys. J. 11:212.) on the dependence of S(f) on the mean steady-state current and the external potassium concentration. We also calculate the mean channel density and the Frank elastic constant of the membrane. This work is an extension of a macroscopic model of Lundström and McQueen (1974, J. Theor. Biol. 45:405.) who obtain a spectral density of the form S approximately /I/2/f.