Abstract
Light transmission changes upon massive stimulation of single muscle fibers of Xenopus were studied with the potential-sensitive nonpermeant dyes, merocyanine rhodanine (WW375) and merocyanine oxazolone (NK2367). Upon stimulation an absorption change (wave a) occurred, which probably represents the sum of action potentials in the transverse tubules and surface membrane. In WW375-stained fibers wave a is a decrease in transmission over the range of 630 to 730 nm (with NK2367, over the range of 590 to 700 nm) but becomes an increase outside this range, thus showing a triphasic spectral pattern. This spectrum differs from that of the squid axon, in which depolarization produces only an increase in transmission over the whole range of wavelengths (Ross et al. 1977. J. Membr. Biol. 33:141-183). When wave a was measured at the edge of the fiber to obtain more signal from the surface membrane, the spectrum did not seem to differ markedly from that obtained from the entire width of the fiber. Thus, the difference in the spectrum between the squid axon and the vertebrate muscle cannot be attributed to the presence of the tubular system.
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Selected References
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- Bastian J., Nakajima S. Action potential in the transverse tubules and its role in the activation of skeletal muscle. J Gen Physiol. 1974 Feb;63(2):257–278. doi: 10.1085/jgp.63.2.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bezanilla F., Horowicz P. Fluorescence intensity changes associated with contractile activation in frog muscle stained with Nile Blue A. J Physiol. 1975 Apr;246(3):709–735. doi: 10.1113/jphysiol.1975.sp010912. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohen L. B., Salzberg B. M., Davila H. V., Ross W. N., Landowne D., Waggoner A. S., Wang C. H. Changes in axon fluorescence during activity: molecular probes of membrane potential. J Membr Biol. 1974;19(1):1–36. doi: 10.1007/BF01869968. [DOI] [PubMed] [Google Scholar]
- Cohen L. B., Salzberg B. M., Davila H. V., Ross W. N., Landowne D., Waggoner A. S., Wang C. H. Changes in axon fluorescence during activity: molecular probes of membrane potential. J Membr Biol. 1974;19(1):1–36. doi: 10.1007/BF01869968. [DOI] [PubMed] [Google Scholar]
- Cohen L. B., Salzberg B. M. Optical measurement of membrane potential. Rev Physiol Biochem Pharmacol. 1978;83:35–88. doi: 10.1007/3-540-08907-1_2. [DOI] [PubMed] [Google Scholar]
- Costantin L. L. The role of sodium current in the radial spread of contraction in frog muscle fibers. J Gen Physiol. 1970 Jun;55(6):703–715. doi: 10.1085/jgp.55.6.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gilai A., Kirsch G. E. Latency-relaxation in single muscle fibres. J Physiol. 1978 Sep;282:197–205. doi: 10.1113/jphysiol.1978.sp012457. [DOI] [PMC free article] [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]
- HUXLEY A. F., TAYLOR R. E. Local activation of striated muscle fibres. J Physiol. 1958 Dec 30;144(3):426–441. doi: 10.1113/jphysiol.1958.sp006111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Matsumura M. On the nature of the latency relaxation of frog skeletal muscle. Jpn J Physiol. 1969 Dec;19(6):701–711. doi: 10.2170/jjphysiol.19.701. [DOI] [PubMed] [Google Scholar]
- Mobley B. A., Eisenberg B. R. Sizes of components in frog skeletal muscle measured by methods of stereology. J Gen Physiol. 1975 Jul;66(1):31–45. doi: 10.1085/jgp.66.1.31. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morad M., Salama G. Optical probes of membrane potential in heart muscle. J Physiol. 1979 Jul;292:267–295. doi: 10.1113/jphysiol.1979.sp012850. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mulieri L. A. The dependence of the latency relaxation on sarcomere length and other characteristics of isolated muscle fibres. J Physiol. 1972 Jun;223(2):333–354. doi: 10.1113/jphysiol.1972.sp009850. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nakajima S., Gilai A., Dingeman D. Dye absorption changes in single muscle fibers: an application of an automatic balancing circuit. Pflugers Arch. 1976 Apr 6;362(3):285–287. doi: 10.1007/BF00581183. [DOI] [PubMed] [Google Scholar]
- Nakajima S., Gilai A. Radial propagation of muscle action potential along the tubular system examined by potential-sensitive dyes. J Gen Physiol. 1980 Dec;76(6):751–762. doi: 10.1085/jgp.76.6.751. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oetliker H., Baylor S. M., Chandler W. K. Simultaneous changes in fluorescence and optical retardation in single muscle fibres during activity. Nature. 1975 Oct 23;257(5528):693–696. doi: 10.1038/257693a0. [DOI] [PubMed] [Google Scholar]
- Peachey L. D. The sarcoplasmic reticulum and transverse tubules of the frog's sartorius. J Cell Biol. 1965 Jun;25(3 Suppl):209–231. doi: 10.1083/jcb.25.3.209. [DOI] [PubMed] [Google Scholar]
- Ross W. N., Reichardt L. F. Species-specific effects on the optical signals of voltage-sensitive dyes. J Membr Biol. 1979 Aug;48(4):343–356. doi: 10.1007/BF01869445. [DOI] [PubMed] [Google Scholar]
- Ross W. N., Salzberg B. M., Cohen L. B., Davila H. V. A large change in dye absorption during the action potential. Biophys J. 1974 Dec;14(12):983–986. doi: 10.1016/S0006-3495(74)85963-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ross W. N., Salzberg B. M., Cohen L. B., Grinvald A., Davila H. V., Waggoner A. S., Wang C. H. Changes in absorption, fluorescence, dichroism, and Birefringence in stained giant axons: : optical measurement of membrane potential. J Membr Biol. 1977 May 6;33(1-2):141–183. doi: 10.1007/BF01869514. [DOI] [PubMed] [Google Scholar]
- Tasaki I., Warashina A. Dye-membrane interaction and its changes during nerve excitation. Photochem Photobiol. 1976 Aug;24(2):191–207. doi: 10.1111/j.1751-1097.1976.tb06810.x. [DOI] [PubMed] [Google Scholar]
- Tasaki I., Watanabe A., Sandlin R., Carnay L. Changes in fluorescence, turbidity, and birefringence associated with nerve excitation. Proc Natl Acad Sci U S A. 1968 Nov;61(3):883–888. doi: 10.1073/pnas.61.3.883. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vergara J., Bezanilla F. Fluorescence changes during electrical activity in frog muscle stained with merocyanine. Nature. 1976 Feb 26;259(5545):684–686. doi: 10.1038/259684a0. [DOI] [PubMed] [Google Scholar]
- Vergara J., Bezanilla F., Salzberg B. M. Nile blue fluorescence signals from cut single muscle fibers under voltage or current clamp conditions. J Gen Physiol. 1978 Dec;72(6):775–800. doi: 10.1085/jgp.72.6.775. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waggoner A. S. Dye indicators of membrane potential. Annu Rev Biophys Bioeng. 1979;8:47–68. doi: 10.1146/annurev.bb.08.060179.000403. [DOI] [PubMed] [Google Scholar]
- Waggoner A. S., Grinvald A. Mechanisms of rapid optical changes of potential sensitive dyes. Ann N Y Acad Sci. 1977 Dec 30;303:217–241. [PubMed] [Google Scholar]
- Waggoner A. Optical probes of membrane potential. J Membr Biol. 1976 Jun 30;27(4):317–334. doi: 10.1007/BF01869143. [DOI] [PubMed] [Google Scholar]