|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
A comparison of propagated action potentials from tropical and temperate squid axons: different durations and conduction velocities correlate with ionic conductance levels
Departments of Physiology and Anesthesiology, UCLA School of Medicine, Los Angeles, CA 90095, USA
* Author for correspondence (e-mail: fbezanil{at}ucla.edu )
Accepted 5 April 2002
To determine which physiological properties contribute to temperature adaptation in the squid giant axon, action potentials were recorded from four species of squid whose habitats span a temperature range of 20°C. The environments of these species can be ranked from coldest to warmest as follows: Loligo opalescens>Loligo pealei>Loligo plei>Sepioteuthis sepioidea. Action potential conduction velocities and rise times, recorded at many temperatures, were equivalent for all Loligo species, but significantly slower in S. sepioidea. By contrast, the action potential's fall time differed among species and correlated well with the thermal environment of the species (`warmer' species had slower decay times). The biophysical underpinnings of these differences were examined in voltage-clamped axons. Surprisingly, no differences were found between the activation kinetics or voltage-dependence of Na+ and K+ currents. Conductance levels, however, did vary. Maximum Na+ conductance (gNa) in S. sepiodea was significantly less than in the Loligo species. K+ conductance (gK) was highest in L. pealei, intermediate in L. plei and smallest in S. sepiodea. The time course and magnitude of gK and gNa were measured directly during membrane action potentials. These data reveal clear species-dependent differences in the amount of gK and gNa recruited during an action potential.
Key words: squid, giant axon, Loligo pealei, Loligo opalescens, Loligo plei, Sepioteuthis sepioidea, temperature adaptation, action potential, conduction velocity, K+ conductance, Na+ conductance, K+ current, Na+ current, conduction velocity, action potential broadening
Related articles in JEB:
This article has been cited by other articles:
![]() |
P. Crotty, T. Sangrey, and W. B Levy Metabolic Energy Cost of Action Potential Velocity J Neurophysiol, September 1, 2006; 96(3): 1237 - 1246. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. M. Leao, C. Kushmerick, R. Pinaud, R. Renden, G.-L. Li, H. Taschenberger, G. Spirou, S. R. Levinson, and H. von Gersdorff Presynaptic Na+ Channels: Locus, Development, and Recovery from Inactivation at a High-Fidelity Synapse J. Neurosci., April 6, 2005; 25(14): 3724 - 3738. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. G. A. Money, M. L. Anstey, and R. M. Robertson Heat Stress-Mediated Plasticity in a Locust Looming-Sensitive Visual Interneuron J Neurophysiol, April 1, 2005; 93(4): 1908 - 1919. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Haverinen and M. Vornanen Temperature acclimation modifies Na+ current in fish cardiac myocytes J. Exp. Biol., July 15, 2004; 207(16): 2823 - 2833. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. M. Robertson Modulation of Neural Circuit Operation by Prior Environmental Stress Integr. Comp. Biol., February 1, 2004; 44(1): 21 - 27. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. J. Lang and J. Rosenbluth Role of Myelination in the Development of a Uniform Olivocerebellar Conduction Time J Neurophysiol, April 1, 2003; 89(4): 2259 - 2270. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. R. Clay On the Persistent Sodium Current in Squid Giant Axons J Neurophysiol, January 1, 2003; 89(1): 640 - 644. [Abstract] [Full Text] [PDF] |
||||