Abstract
Lobster and squid giant nerve fibers respond differently when subjected to osmotic challenges. The axons proper, as distinct from the total (fiber) complex formed by the axon and connective sheath, both behave as "fast" osmometers for changes in the concentration of NaCl, but the maximum degree of swelling in hyposmotic media is by about 60% in lobster and only by 20% in squid. The relative volume intercepts of the van't Hoff relation are about 0.2 for lobster and 0.4 for squid. The sheaths of both axons undergo only small, apparently passive changes in volume. Lobster axons are permeable to Cl, but squid axons are impermeable to this anion. Lobster axons are also permeable to glycerol. The implications of the data as to the nature of volume regulation of cells are discussed.
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Selected References
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- ADRIAN R. H. Potassium chloride movement and the membrane potential of frog muscle. J Physiol. 1960 Apr;151:154–185. [PMC free article] [PubMed] [Google Scholar]
- BAKER P. F., HODGKIN A. L., MEVES H. THE EFFECT OF DILUTING THE INTERNAL SOLUTION ON THE ELECTRICAL PROPERTIES OF A PERFUSED GIANT AXON. J Physiol. 1964 Apr;170:541–560. doi: 10.1113/jphysiol.1964.sp007348. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BAKER P. F., HODGKIN A. L., SHAW T. I. Replacement of the axoplasm of giant nerve fibres with artificial solutions. J Physiol. 1962 Nov;164:330–354. doi: 10.1113/jphysiol.1962.sp007025. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boyle P. J., Conway E. J. Potassium accumulation in muscle and associated changes. J Physiol. 1941 Aug 11;100(1):1–63. doi: 10.1113/jphysiol.1941.sp003922. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brandt P. W., Reuben J. P., Girardier L., Grundfest H. Correlated morphological and physiological studies on isolated single muscle fibers. I. Fine structure of the crayfish muscle fiber. J Cell Biol. 1965 Jun;25(3 Suppl):233–260. doi: 10.1083/jcb.25.3.233. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CARMELIET E. E. Chloride ions and the membrane potential of Purkinje fibres. J Physiol. 1961 Apr;156:375–388. doi: 10.1113/jphysiol.1961.sp006682. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chandler W. K., Hodgkin A. L. The effect of internal sodium on the action potential in the presence of different internal anions. J Physiol. 1965 Dec;181(3):594–611. doi: 10.1113/jphysiol.1965.sp007785. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DALTON J. C. Effects of external ions on membrane potentials of a lobster giant axon. J Gen Physiol. 1958 Jan 20;41(3):529–542. doi: 10.1085/jgp.41.3.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ENDO M. ENTRY OF A DYE INTO THE SARCOTUBULAR SYSTEM OF MUSCLE. Nature. 1964 Jun 13;202:1115–1116. doi: 10.1038/2021115b0. [DOI] [PubMed] [Google Scholar]
- FRANKENHAEUSER B., HODGKIN A. L. The action of calcium on the electrical properties of squid axons. J Physiol. 1957 Jul 11;137(2):218–244. doi: 10.1113/jphysiol.1957.sp005808. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GIRARDIER L., REUBEN J. P., BRANDT P. W., GRUNDFEST H. EVIDENCE FOR ANION-PERMSELECTIVE MEMBRANE IN CRAYFISH MUSCLE FIBERS AND ITS POSSIBLE ROLE IN EXCITATION-CONTRACTION COUPLING. J Gen Physiol. 1963 Sep;47:189–214. doi: 10.1085/jgp.47.1.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GRUNDFEST H., KAO C. Y., ALTAMIRANO M. Bioelectric effects of ions microinjected into the giant axon of Loligo. J Gen Physiol. 1954 Nov 20;38(2):245–282. doi: 10.1085/jgp.38.2.245. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grundfest H. Heterogeneity of excitable membrane: electrophysiological and pharmacological evidence and some consequences. Ann N Y Acad Sci. 1966 Jul 14;137(2):901–949. doi: 10.1111/j.1749-6632.1966.tb50208.x. [DOI] [PubMed] [Google Scholar]
- HODGKIN A. L., HOROWICZ P. The influence of potassium and chloride ions on the membrane potential of single muscle fibres. J Physiol. 1959 Oct;148:127–160. doi: 10.1113/jphysiol.1959.sp006278. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HODGKIN A. L., KATZ B. The effect of sodium ions on the electrical activity of giant axon of the squid. J Physiol. 1949 Mar 1;108(1):37–77. doi: 10.1113/jphysiol.1949.sp004310. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HUXLEY H. E. EVIDENCE FOR CONTINUITY BETWEEN THE CENTRAL ELEMENTS OF THE TRIADS AND EXTRACELLULAR SPACE IN FROG SARTORIUS MUSCLE. Nature. 1964 Jun 13;202:1067–1071. doi: 10.1038/2021067b0. [DOI] [PubMed] [Google Scholar]
- JULIAN F. J., MOORE J. W., GOLDMAN D. E. Membrane potentials of the lobster giant axon obtained by use of the sucrose-gap technique. J Gen Physiol. 1962 Jul;45:1195–1216. doi: 10.1085/jgp.45.6.1195. [DOI] [PMC free article] [PubMed] [Google Scholar]
- REUBEN J. P., GIRARDIER L., GRUNDFEST H. WATER TRANSFER AND CELL STRUCTURE IN ISOLATED CRAYFISH MUSCLE FIBERS. J Gen Physiol. 1964 Jul;47:1141–1174. doi: 10.1085/jgp.47.6.1141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- REUBER J. P., LOPEZ E., BRANDT P. W., GRUNDFEST H. MUSCLE: VOLUME CHANGES IN ISOLATED SINGLE FIBERS. Science. 1963 Oct 11;142(3589):246–248. doi: 10.1126/science.142.3589.246. [DOI] [PubMed] [Google Scholar]
- VILLEGAS R., BARNOLA F. V. Characterization of the resting axolemma in the giant axon of the squid. J Gen Physiol. 1961 May;44:963–977. doi: 10.1085/jgp.44.5.963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- VILLEGAS R., CAPUTO C., VILLEGAS L. Diffusion barrieres in the squid nerve fiber. The axolemma and the Schwann layer. J Gen Physiol. 1962 Nov;46:245–255. doi: 10.1085/jgp.46.2.245. [DOI] [PMC free article] [PubMed] [Google Scholar]
- VILLEGAS R., VILLEGAS G. M. Characterization of the membranes in the giant nerve fiber of the squid. J Gen Physiol. 1960 May;43:73–103. doi: 10.1085/jgp.43.5.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WRIGHT E. B., REUBEN J. P. A comparative study of some excitability properties of the giant axons of the ventral nerve cord of the lobster, including the recovery of excitability following an impulse. J Cell Physiol. 1958 Feb;51(1):13–28. doi: 10.1002/jcp.1030510103. [DOI] [PubMed] [Google Scholar]
