Literature DB >> 3260626

Voltage sensors of the frog skeletal muscle membrane require calcium to function in excitation-contraction coupling.

G Brum1, R Fitts, G Pizarro, E Ríos.   

Abstract

1. Intramembrane charge movements and changes in intracellular Ca2+ concentration (Ca2+ transients) elicited by pulse depolarization were measured in frog fast twitch cut muscle fibres under voltage clamp. 2. Extracellular solutions with very low [Ca2+] and 2 mM-Mg2+ , shown in the previous paper to reduce Ca2+ release from the sarcoplasmic reticulum (SR), were found to cause two changes in charge movement: (a) a decrease (-12 nC/microF) in the charge that moves during depolarizing pulses from -90 to 0 mV, termed here 'charge 1'; (b) an increase (+7 nC/microF) in the charge moved by hyperpolarizing pulses from -90 to -180 mV, termed 'charge 2'. 3. The increase in charge moved by hyperpolarizing pulses was correlated (r = 0.64) with the decrease in charge moved by depolarizing pulses and both were correlated with the inhibition of Ca2+ release recorded in the same fibres. 4. The low Ca2+ solutions caused a shift to more negative voltages of the dependence relating charge movement and holding potential (VH). This shift is of similar magnitude (about 22 mV) and direction as the shift in the curve relating Ca2+ release flux to VH (previous paper). 5. In solutions with normal [Ca2+] a conditioning depolarization to 0 mV, of 2 s duration, placed 100 ms before a test pulse from -70 to 0 mV, reduced by 30% the amount of charge displaced by the test pulse. Conditioning pulses of 1 s or less caused potentiation of charge movement by up to 30%. 6. In low Ca2+ solutions, reduction of charge was observed at all durations of the conditioning pulse. The duration for half-inhibition was near 200 ms. 7. An extracellular solution with no metal cations caused a more radical inhibition than the low Ca2+ solutions that contained Mg2+. The inhibition of Ca2+ release was essentially complete (90-100%). The charge moved by a pulse to 0 mV was reduced by 20 nC/microF and the charge moved by a pulse to -170 mV increased 8 nC/microF. This shows that Mg2+ supports excitation-contraction (E-C) coupling to some extent. 8. A state model of the voltage sensor of E-C coupling explains qualitatively the observations in both papers.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3260626      PMCID: PMC1191783          DOI: 10.1113/jphysiol.1988.sp017053

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  31 in total

Review 1.  Excitation-contraction coupling in skeletal muscle.

Authors:  J Caillé; M Ildefonse; O Rougier
Journal:  Prog Biophys Mol Biol       Date:  1985       Impact factor: 3.667

2.  Intramembrane charge movement in frog skeletal muscle fibres. Properties of charge 2.

Authors:  G Brum; E Rios
Journal:  J Physiol       Date:  1987-06       Impact factor: 5.182

3.  Asymmetric charge movement in polarized and depolarized muscle fibres of the rabbit.

Authors:  G D Lamb
Journal:  J Physiol       Date:  1987-02       Impact factor: 5.182

4.  Charge movement and membrane capacity in frog muscle.

Authors:  R H Adrian; A Peres
Journal:  J Physiol       Date:  1979-04       Impact factor: 5.182

5.  Time course of calcium release and removal in skeletal muscle fibers.

Authors:  W Melzer; E Rios; M F Schneider
Journal:  Biophys J       Date:  1984-03       Impact factor: 4.033

6.  A comparative study of charge movement in rat and frog skeletal muscle fibres.

Authors:  S Hollingworth; M W Marshall
Journal:  J Physiol       Date:  1981-12       Impact factor: 5.182

7.  Effects of glycerol treatment and maintained depolarization on charge movement in skeletal muscle.

Authors:  W K Chandler; R F Rakowski; M F Schneider
Journal:  J Physiol       Date:  1976-01       Impact factor: 5.182

8.  Paralysis of frog skeletal muscle fibres by the calcium antagonist D-600.

Authors:  R S Eisenberg; R T McCarthy; R L Milton
Journal:  J Physiol       Date:  1983-08       Impact factor: 5.182

9.  Effects of the calcium antagonist gallopamil (D600) upon excitation-contraction coupling in toe muscle fibres of the frog.

Authors:  D Berwe; G Gottschalk; H C Lüttgau
Journal:  J Physiol       Date:  1987-04       Impact factor: 5.182

10.  Perchlorate and the relationship between charge movement and contractile activation in frog skeletal muscle fibres.

Authors:  L Csernoch; L Kovács; G Szücs
Journal:  J Physiol       Date:  1987-09       Impact factor: 5.182

View more
  67 in total

Review 1.  Calcium release in skeletal muscle: from K+ contractures to Ca2+ sparks.

Authors:  C Caputo
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

2.  Intracellular Ca(2+) release as irreversible Markov process.

Authors:  Juliana Rengifo; Rafael Rosales; Adom González; Heping Cheng; Michael D Stern; Eduardo Ríos
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

3.  Dihydropyridine-induced Ca2+ release from ryanodine-sensitive Ca2+ pools in human skeletal muscle cells.

Authors:  L G Weigl; M Hohenegger; H G Kress
Journal:  J Physiol       Date:  2000-06-01       Impact factor: 5.182

4.  Two components of voltage-dependent inactivation in Ca(v)1.2 channels revealed by its gating currents.

Authors:  Gonzalo Ferreira; Eduardo Ríos; Nicolás Reyes
Journal:  Biophys J       Date:  2003-06       Impact factor: 4.033

5.  Effects of the enantiomers of BayK 8644 on the charge movement of L-type Ca channels in guinea-pig ventricular myocytes.

Authors:  P Artigas; G Ferreira; N Reyes; G Brum; G Pizarro
Journal:  J Membr Biol       Date:  2003-06-01       Impact factor: 1.843

6.  Ca2+ current and charge movement in adult single human skeletal muscle fibres.

Authors:  J García; K McKinley; S H Appel; E Stefani
Journal:  J Physiol       Date:  1992-08       Impact factor: 5.182

7.  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

8.  The effect of the phenylalkylamine D888 (devapamil) on force and Ca2+ current in isolated frog skeletal muscle fibres.

Authors:  R Erdmann; H C Lüttgau
Journal:  J Physiol       Date:  1989-06       Impact factor: 5.182

9.  The action of ryanodine on rat fast and slow intact skeletal muscles.

Authors:  M W Fryer; G D Lamb; I R Neering
Journal:  J Physiol       Date:  1989-07       Impact factor: 5.182

10.  How source content determines intracellular Ca2+ release kinetics. Simultaneous measurement of [Ca2+] transients and [H+] displacement in skeletal muscle.

Authors:  Gonzalo Pizarro; Eduardo Ríos
Journal:  J Gen Physiol       Date:  2004-09       Impact factor: 4.086

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.