Literature DB >> 1713947

Interfering with calcium release suppresses I gamma, the "hump" component of intramembranous charge movement in skeletal muscle.

L Csernoch1, G Pizarro, I Uribe, M Rodríguez, E Ríos.   

Abstract

Four manifestations of excitation-contraction (E-C) coupling were derived from measurements in cut skeletal muscle fibers of the frog, voltage clamped in a Vaseline-gap chamber: intramembranous charge movement currents, myoplasmic [Ca2+] transients, flux of calcium release from the sarcoplasmic reticulum (SR), and the intrinsic optical transparency change that accompanies calcium release. In attempts to suppress Ca release by direct effects on the SR, three interventions were applied: (a) a conditioning pulse that causes calcium release and inhibits release in subsequent pulses by Ca-dependent inactivation; (b) a series of brief, large pulses, separated by long intervals (greater than 700 ms), which deplete Ca2+ in the SR; and (c) intracellular application of the release channel blocker ruthenium red. All these reduced calcium release flux. None was expected to affect directly the voltage sensor of the T-tubule; however, all of them reduced or eliminated a component of charge movement current with the following characteristics: (a) delayed onset, peaking 10-20 ms into the pulse; (b) current reversal during the pulse, with an inward phase after the outward peak; and (c) OFF transient of smaller magnitude than the ON, of variable polarity, and sometimes biphasic. When the total charge movement current had a visible hump, the positive phase of the current eliminated by the interventions agreed with the hump in timing and size. The component of charge movement current blocked by the interventions was greater and had a greater inward phase in slack fibers with high [EGTA] inside than in stretched fibers with no EGTA. Its amplitude at -40 mV was on average 0.26 A/F (SEM 0.03) in slack fibers. The waveform of release flux determined from the Ca transients measured simultaneously with the membrane currents had, as described previously (Melzer, W., E. Ríos, and M. F. Schneider. 1984. Biophysical Journal. 45:637-641), an early peak followed by a descent to a steady level during the pulse. The time at which this peak occurred was highly correlated with the time to peak of the current suppressed, occurring on average 6.9 ms later (SEM 0.73 ms). The current suppressed by the above interventions in all cases had a time course similar to the time derivative of the release flux; specifically, the peak of the time derivative of release flux preceded the peak of the current suppressed by 0.7 ms (SEM 0.6 ms). The magnitude of the current blocked was highly correlated with the inhibitory effect of the interventions on Ca2+ release flux.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1713947      PMCID: PMC2216499          DOI: 10.1085/jgp.97.5.845

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  49 in total

1.  Inhibitors of Ca2+ release from the isolated sarcoplasmic reticulum. I. Ca2+ channel blockers.

Authors:  B Antoniu; D H Kim; M Morii; N Ikemoto
Journal:  Biochim Biophys Acta       Date:  1985-06-11

2.  Purified ryanodine receptor from skeletal muscle sarcoplasmic reticulum is the Ca2+-permeable pore of the calcium release channel.

Authors:  T Imagawa; J S Smith; R Coronado; K P Campbell
Journal:  J Biol Chem       Date:  1987-12-05       Impact factor: 5.157

3.  Ryanodine receptor of skeletal muscle is a gap junction-type channel.

Authors:  J Ma; M Fill; C M Knudson; K P Campbell; R Coronado
Journal:  Science       Date:  1988-10-07       Impact factor: 47.728

Review 4.  Intramembrane charge movements in skeletal muscle.

Authors:  C L Huang
Journal:  Physiol Rev       Date:  1988-10       Impact factor: 37.312

5.  Purification and reconstitution of the calcium release channel from skeletal muscle.

Authors:  F A Lai; H P Erickson; E Rousseau; Q Y Liu; G Meissner
Journal:  Nature       Date:  1988-01-28       Impact factor: 49.962

6.  Changes in light scattered by striated muscle during excitation-contraction coupling.

Authors:  W H Barry; L D Carnay
Journal:  Am J Physiol       Date:  1969-11

7.  Sarcoplasmic reticulum contains adenine nucleotide-activated calcium channels.

Authors:  J S Smith; R Coronado; G Meissner
Journal:  Nature       Date:  1985 Aug 1-7       Impact factor: 49.962

8.  Calcium-ryanodine receptor complex. Solubilization and partial characterization from skeletal muscle junctional sarcoplasmic reticulum vesicles.

Authors:  I N Pessah; A O Francini; D J Scales; A L Waterhouse; J E Casida
Journal:  J Biol Chem       Date:  1986-07-05       Impact factor: 5.157

9.  Anatomical distribution of voltage-dependent membrane capacitance in frog skeletal muscle fibers.

Authors:  C L Huang; L D Peachey
Journal:  J Gen Physiol       Date:  1989-03       Impact factor: 4.086

Review 10.  Calcium-gated calcium channels in sarcoplasmic reticulum of rabbit skinned skeletal muscle fibers.

Authors:  P Volpe; G Salviati; A Chu
Journal:  J Gen Physiol       Date:  1986-02       Impact factor: 4.086

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  43 in total

1.  Regulation of the rat sarcoplasmic reticulum calcium release channel by calcium.

Authors:  S Sárközi; C Szegedi; P Szentesi; L Csernoch; L Kovács; I Jóna
Journal:  J Muscle Res Cell Motil       Date:  2000-02       Impact factor: 2.698

2.  Association of the Igamma and Idelta charge movement with calcium release in frog skeletal muscle.

Authors:  Chiu Shuen Hui
Journal:  Biophys J       Date:  2004-11-08       Impact factor: 4.033

Review 3.  The mechanical hypothesis of excitation-contraction (EC) coupling in skeletal muscle.

Authors:  E Ríos; J J Ma; A González
Journal:  J Muscle Res Cell Motil       Date:  1991-04       Impact factor: 2.698

4.  The relationship between Q gamma and Ca release from the sarcoplasmic reticulum in skeletal muscle.

Authors:  G Pizarro; L Csernoch; I Uribe; M Rodríguez; E Ríos
Journal:  J Gen Physiol       Date:  1991-05       Impact factor: 4.086

5.  Differential effects of tetracaine on two kinetic components of calcium release in frog skeletal muscle fibres.

Authors:  G Pizarro; L Csernoch; I Uribe; E Ríos
Journal:  J Physiol       Date:  1992-11       Impact factor: 5.182

6.  The Qgamma component of intra-membrane charge movement is present in mammalian muscle fibres, but suppressed in the absence of S100A1.

Authors:  Benjamin L Prosser; Erick O Hernández-Ochoa; Danna B Zimmer; Martin F Schneider
Journal:  J Physiol       Date:  2009-08-03       Impact factor: 5.182

7.  A possible role of sarcoplasmic Ca2+ release in modulating the slow Ca2+ current of skeletal muscle.

Authors:  D Feldmeyer; W Melzer; B Pohl; P Zöllner
Journal:  Pflugers Arch       Date:  1993-10       Impact factor: 3.657

8.  Differential suppression of charge movement components by gluconate in cut twitch fibres of Rana temporaria.

Authors:  C S Hui; W Chen
Journal:  J Physiol       Date:  1995-12-01       Impact factor: 5.182

9.  Dual actions of tetracaine on intramembrane charge in amphibian striated muscle.

Authors:  C L Huang
Journal:  J Physiol       Date:  1997-06-15       Impact factor: 5.182

10.  Charge movements in intact amphibian skeletal muscle fibres in the presence of cardiac glycosides.

Authors:  C L Huang
Journal:  J Physiol       Date:  2001-04-15       Impact factor: 5.182

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