Abstract
A cephalin-cholesterol membrane model is described whose electrical resistance can be reversibly raised by CaCl2 or lowered by KCl or NaCl whether these ions are added to the membrane by mechanical immersion or are driven in electrically. Either KCl or NaCl acts antagonistically to CaCl2. Experiments with controlled pH indicate that the above effects depend somehow on combination of the cations with the phospholipid acidic groups. Also, they are correlated with decreased membrane hydration in CaCl2 solutions, and increased hydration in KCl or NaCl solutions. It is conjectured that cells may regulate their transsurface ion pathways and fluxes by K-Ca competition for negatively charged binding sites on plasma membrane phospholipid. It is regarded as a corollary to say that a fundamental event in excitation is displacement of membrane Ca from such a site by catelectrotonically propelled K.
Full Text
The Full Text of this article is available as a PDF (739.4 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BIANCHI C. P., SHANES A. M. Calcium influx in skeletal muscle at rest, during activity, and during potassium contracture. J Gen Physiol. 1959 Mar 20;42(4):803–815. doi: 10.1085/jgp.42.4.803. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BRYANT S. H., TOBIAS J. M. Changes in light scattering accompanying activity in nerve. J Cell Physiol. 1952 Oct;40(2):199–219. doi: 10.1002/jcp.1030400204. [DOI] [PubMed] [Google Scholar]
- BRYANT S. H., TOBIAS J. M. Optical and mechanical concomitants of activity in Carcinus nerve. I. Effect of sodium azide on the optical response. II. Shortening of the nerve with activity. J Cell Physiol. 1955 Aug;46(1):71–95. doi: 10.1002/jcp.1030460105. [DOI] [PubMed] [Google Scholar]
- FINEAN J. B. The molecular organisation of nerve myelin. Acta Neurol Psychiatr Belg. 1957 May;57(5):462–471. [PubMed] [Google Scholar]
- Geren B. B., Schmitt F. O. 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 Sep;40(9):863–870. doi: 10.1073/pnas.40.9.863. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HILL D. K. The effect of stimulation on the opacity of a crustacean nerve trunk and its relation to fibre diameter. J Physiol. 1950 Oct 16;111(3-4):283–303. doi: 10.1113/jphysiol.1950.sp004480. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HILL D. K. The volume change resulting from stimulation of a giant nerve fibre. J Physiol. 1950 Oct 16;111(3-4):304–327. doi: 10.1113/jphysiol.1950.sp004481. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KOKETSU K., MIYAMOTO S. Significance of membrane calcium in calcium-free and potassium-rich media. Nature. 1961 Feb 4;189:403–404. doi: 10.1038/189403a0. [DOI] [PubMed] [Google Scholar]
- SHAW S. N., TOBIAS J. M. On the optical change associated with activity in frog nerve. J Cell Physiol. 1955 Aug;46(1):53–70. doi: 10.1002/jcp.1030460104. [DOI] [PubMed] [Google Scholar]
- TOBIAS J. M. Experimentally altered structure related to function in the lobster axon with an extrapolation to molecular mechanisms in excitation. J Cell Physiol. 1958 Aug;52(1):89–125. doi: 10.1002/jcp.1030520107. [DOI] [PubMed] [Google Scholar]
- TOBIAS J. M. Qualitative observations on visible changes in single frog, squid and other axones subjected to electrical polarization; implications for excitation and conduction. J Cell Physiol. 1951 Feb;37(1):91–105. doi: 10.1002/jcp.1030370107. [DOI] [PubMed] [Google Scholar]
- TOBIAS J. M. Some optically detectable consequences of activity in nerve. Cold Spring Harb Symp Quant Biol. 1952;17:15–25. doi: 10.1101/sqb.1952.017.01.004. [DOI] [PubMed] [Google Scholar]
