Abstract
1. Soleus muscles of anaesthetized rats were stimulated tetanically (4 s at 20 Hz every 5 s for 5 min), following which the resting and action potentials were measured in surface fibres. 2. At the end of the stimulation period, the mean resting potential was found to have increased from a control value of -79.5 +/- 4.8 mV (mean +/- S.D.) to -90.5 +/- 6.3 mV. The hyperpolarization started to decline after 9 min but was still present at 15 min. 3. Associated with the membrane hyperpolarization was an increase in the mean amplitude of the muscle fibre action potential, from 82.2 +/- 10.8 to 96.8 +/- 10.0 mV. 4. Both the hyperpolarization and the enlargement of the muscle fibre action potential were abolished by 1.25 X 10(-4) M-ouabain, cooling the bathing fluid to 19 degrees C or removing K+ from the bathing fluid. 5. The results are explained in terms of an increase in electrogenic sodium pump activity resulting from tetanic stimulation. When the bathing fluid contained 20 mM-K+, the mean resting potential of stimulated fibres was approximately -30 mV greater than that calculated from the Goldman-Hodgkin-Katz equation. 6. The increase in sodium pumping not only acts to restore the concentrations of Na+ and K+ on either side of the muscle fibre membrane, but, through its electrogenic effect, enables fibres to remain excitable during continuous contractile activity.
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- ADRIAN R. H. The effect of internal and external potassium concentration on the membrane potential of frog muscle. J Physiol. 1956 Sep 27;133(3):631–658. doi: 10.1113/jphysiol.1956.sp005615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bigland-Ritchie B., Jones D. A., Woods J. J. Excitation frequency and muscle fatigue: electrical responses during human voluntary and stimulated contractions. Exp Neurol. 1979 May;64(2):414–427. doi: 10.1016/0014-4886(79)90280-2. [DOI] [PubMed] [Google Scholar]
- Brodal B. P., Eeg-Larsen N. L., Iversen O. J., Jebens E., Roed A. Enhanced (Na+, K+)-activated ATPase activity after indirect electric stimulation of rat skeletal muscle in vivo. Life Sci. 1975 Aug 1;17(3):329–331. doi: 10.1016/0024-3205(75)90480-4. [DOI] [PubMed] [Google Scholar]
- CREESE R., HASHISH S. E., SCHOLES N. W. Potassium movements in contracting diaphragm muscle. J Physiol. 1958 Sep 23;143(2):307–324. doi: 10.1113/jphysiol.1958.sp006061. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CREESE R. Measurement of cation fluxes in rat diaphragm. Proc R Soc Lond B Biol Sci. 1954 Sep 27;142(909):497–513. doi: 10.1098/rspb.1954.0039. [DOI] [PubMed] [Google Scholar]
- CREESE R., NORTHOVER J. Maintenance of isolated diaphragm with normal sodium content. J Physiol. 1961 Feb;155:343–357. doi: 10.1113/jphysiol.1961.sp006632. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Clausen T., Everts M. E., Kjeldsen K. Quantification of the maximum capacity for active sodium-potassium transport in rat skeletal muscle. J Physiol. 1987 Jul;388:163–181. doi: 10.1113/jphysiol.1987.sp016608. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Creese R., Head S. D., Jenkinson D. F. The role of the sodium pump during prolonged end-plate currents in guinea-pig diaphragm. J Physiol. 1987 Mar;384:377–403. doi: 10.1113/jphysiol.1987.sp016460. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fitch S., McComas A. Influence of human muscle length on fatigue. J Physiol. 1985 May;362:205–213. doi: 10.1113/jphysiol.1985.sp015671. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fong C. N., Atwood H. L., Charlton M. P. Intracellular sodium-activity at rest and after tetanic stimulation in muscles of normal and dystrophic (dy2J/dy2J) C57BL/6J mice. Exp Neurol. 1986 Aug;93(2):359–368. doi: 10.1016/0014-4886(86)90196-2. [DOI] [PubMed] [Google Scholar]
- Gustafsson B., Wigström H. Hyperpolarization following long-lasting tetanic activation of hippocampal pyramidal cells. Brain Res. 1983 Sep 19;275(1):159–163. doi: 10.1016/0006-8993(83)90429-8. [DOI] [PubMed] [Google Scholar]
- HODGKIN A. L., HUXLEY A. F. A quantitative description of membrane current and its application to conduction and excitation in nerve. J Physiol. 1952 Aug;117(4):500–544. doi: 10.1113/jphysiol.1952.sp004764. [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]
- HODGKIN A. L., KEYNES R. D. Active transport of cations in giant axons from Sepia and Loligo. J Physiol. 1955 Apr 28;128(1):28–60. doi: 10.1113/jphysiol.1955.sp005290. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hanson J. The effects of repetitive stimulation on the action potential and the twitch of rat muscle. Acta Physiol Scand. 1974 Feb;90(2):387–400. doi: 10.1111/j.1748-1716.1974.tb05600.x. [DOI] [PubMed] [Google Scholar]
- Hirche H., Schumacher E., Hagemann H. Extracellular K+ concentration and K+ balance of the gastrocnemius muscle of the dog during exercise. Pflugers Arch. 1980 Sep;387(3):231–237. doi: 10.1007/BF00580975. [DOI] [PubMed] [Google Scholar]
- Hník P., Holas M., Krekule I., Kŭriz N., Mejsnar J., Smiesko V., Ujec E., Vyskocil F. Work-induced potassium changes in skeletal muscle and effluent venous blood assessed by liquid ion-exchanger microelectrodes. Pflugers Arch. 1976 Mar 11;362(1):85–94. doi: 10.1007/BF00588685. [DOI] [PubMed] [Google Scholar]
- Juel C. Potassium and sodium shifts during in vitro isometric muscle contraction, and the time course of the ion-gradient recovery. Pflugers Arch. 1986 May;406(5):458–463. doi: 10.1007/BF00583367. [DOI] [PubMed] [Google Scholar]
- KERNAN R. P. RESTING POTENTIAL OF ISOLATED RAT MUSCLES MEASURED IN PLASMA. Nature. 1963 Nov 2;200:474–475. doi: 10.1038/200474a0. [DOI] [PubMed] [Google Scholar]
- Knochel J. P., Blachley J. D., Johnson J. H., Carter N. W. Muscle cell electrical hyperpolarization and reduced exercise hyperkalemia in physically conditioned dogs. J Clin Invest. 1985 Feb;75(2):740–745. doi: 10.1172/JCI111755. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LILEY A. W. An investigation of spontaneous activity at the neuromuscular junction of the rat. J Physiol. 1956 Jun 28;132(3):650–666. doi: 10.1113/jphysiol.1956.sp005555. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Locke S., Solomon H. C. Relation of resting potential of rat gastrocnemius and soleus muscles to innervation, activity, and the Na-K pump. J Exp Zool. 1967 Dec;166(3):377–386. doi: 10.1002/jez.1401660310. [DOI] [PubMed] [Google Scholar]
- MULLINS L. J., NODA K. THE INFLUENCE OF SODIUM-FREE SOLUTIONS ON THE MEMBRANE POTENTIAL OF FROG MUSCLE FIBERS. J Gen Physiol. 1963 Sep;47:117–132. doi: 10.1085/jgp.47.1.117. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marsden C. D., Meadows J. C., Merton P. A. Isolated single motor units in human muscle and their rate of discharge during maximal voluntary effort. J Physiol. 1971;217 (Suppl):12P–13P. [PubMed] [Google Scholar]
- RITCHIE J. M., STRAUB R. W. The hyperpolarization which follows activity in mammalian non-medullated fibres. J Physiol. 1957 Apr 3;136(1):80–97. doi: 10.1113/jphysiol.1957.sp005744. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SRETER F. A. Distribution of water, sodium, and potassium in resting and stimulated mammalian muscle. Can J Biochem Physiol. 1963 Apr;41:1035–1045. [PubMed] [Google Scholar]
- Thomas R. C. Membrane current and intracellular sodium changes in a snail neurone during extrusion of injected sodium. J Physiol. 1969 Apr;201(2):495–514. doi: 10.1113/jphysiol.1969.sp008769. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vyskocil F., Hník P., Rehfeldt H., Vejsada R., Ujec E. The measurement of K+e concentration changes in human muscles during volitional contractions. Pflugers Arch. 1983 Nov;399(3):235–237. doi: 10.1007/BF00656721. [DOI] [PubMed] [Google Scholar]
- Ward M. R., Thesleff S. The temperature dependence of action potentials in rat skeletal muscle fibres. Acta Physiol Scand. 1974 Aug;91(4):574–576. doi: 10.1111/j.1748-1716.1974.tb05714.x. [DOI] [PubMed] [Google Scholar]
- Williams J. A., Withrow C. D., Woodbury D. M. Effects of ouabain and diphenylhydantoin on transmembrane potentials, intracellular electrolytes, and cell pH of rat muscle and liver in vivo. J Physiol. 1971 Jan;212(1):101–115. doi: 10.1113/jphysiol.1971.sp009312. [DOI] [PMC free article] [PubMed] [Google Scholar]