» Articles » PMID: 13525675

Water Transport in Invertebrate Peripheral Nerve Fibers

Overview
Journal J Gen Physiol
Specialty Physiology
Date 1958 May 20
PMID 13525675
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Osmotic and diffusion permeabilities (P(f) and P(d)) of invertebrate nerve fibers to tritiated water were measured to determine what water flux studies could reveal about "the nerve membrane" and to directly test the possibility of active transport of water into or out of invertebrate nerve fibers. P(f)/P(d) ratios for lobster walking leg nerve fibers were found to be about 20 +/- 7 at 14 degrees C. P(d) measurements were made for squid giant axons at 25 degrees C. and found to yield a value of 4 x 10(-4) cm.(-1) sec.(-1). When combined with the data of D. K. Hill for P(f), a P(f)/P(d) ratio of 21 +/- 5 is obtained. These P(f)/P(d) ratios correspond to "effective pore radii" of about 16 +/- 4 angstrom units, according to theories developed by Koefoed-Johnsen and Ussing and independently by Pappenheimer and his colleagues. Variations of water flux ratios with temperatures were studied and apparent activation energies calculated for both diffusion experiments and osmotic filtration experiments using the Arrhenius equation, and found to be close to 3 to 5 cal. per mole of water transferred. Cyanide (5 x 10(-3) molar) and iodoacetate (1 x 10(-3) molar) poisoned lobster leg nerve fibers showed no appreciable change in diffusion or osmotic filtration water effluxes. Caution in interpreting these proposed channels as simple pores was emphasized, but the possibility that such channels exist and are related to ionic flow is not incompatible with electrophysiological data.

Citing Articles

Water permeability of isolated cuticular membranes: The effect of pH and cations on diffusion, hydrodynamic permeability and size of polar pores in the cutin matrix.

Schonherr J Planta. 2014; 128(2):113-26.

PMID: 24430686 DOI: 10.1007/BF00390312.


The state of water in the outer barrier of the isolated frog skin.

Grigera J, Cereijido M J Membr Biol. 2013; 4(1):148-55.

PMID: 24174235 DOI: 10.1007/BF02431967.


Water Permeability and Cold Hardiness of Cortex Cells in Cornus stolonifera Michx.-A Preliminary Report.

McKenzie J, Weiser C, Stadelmann E, Burke M Plant Physiol. 1974; 54(2):173-6.

PMID: 16658854 PMC: 541525. DOI: 10.1104/pp.54.2.173.


Experimental study of the independence of diffusion and hydrodynamic permeability coefficients in collodion membranes.

Robbins E, Mauro A J Gen Physiol. 1960; 43:523-32.

PMID: 14437747 PMC: 2195022. DOI: 10.1085/jgp.43.3.523.


Diffusion barrieres in the squid nerve fiber. The axolemma and the Schwann layer.

Villegas R, Caputo C, Villegas L J Gen Physiol. 1962; 46:245-55.

PMID: 13997307 PMC: 2195262. DOI: 10.1085/jgp.46.2.245.


References
1.
Prescott D, Zeuthen E . Comparison of water diffusion and water filtration across cell surfaces. Acta Physiol Scand. 1953; 28(1):77-94. DOI: 10.1111/j.1748-1716.1953.tb00960.x. View

2.
Durbin R, Frank H, Solomon A . Water flow through frog gastric mucosa. J Gen Physiol. 1956; 39(4):535-51. PMC: 2147550. DOI: 10.1085/jgp.39.4.535. View

3.
GEREN B, SCHMITT F . THE STRUCTURE OF THE SCHWANN CELL AND ITS RELATION TO THE AXON IN CERTAIN INVERTEBRATE NERVE FIBERS. Proc Natl Acad Sci U S A. 1954; 40(9):863-70. PMC: 534183. DOI: 10.1073/pnas.40.9.863. View

4.
TEORELL T . A contribution to the knowledge of rhythmical transport processes of water and salts. Exp Cell Res. 1955; (Suppl 3):339-45. View

5.
AEBI H . [Connections between respiration swelling & electrolyte content of surviving tissue specimen]. Helv Physiol Pharmacol Acta. 1952; 10(2):184-206. View