Literature DB >> 3158652

Electron probe X-ray microanalysis of post-tetanic Ca2+ and Mg2+ movements across the sarcoplasmic reticulum in situ.

A V Somlyo, G McClellan, H Gonzalez-Serratos, A P Somlyo.   

Abstract

Ca2+ and Mg2+ movements across the sarcoplasmic reticulum (SR) of frog skeletal muscle fibers were measured in situ by electron probe microanalysis of muscles rapidly frozen following a tetanus. At 400 ms following a 1.2-s tetanus at room temperature, the force had relaxed to base-line, and 0.3 mmol of Ca2+/liter of cytoplasmic H2O had been pumped by the SR, indicating that the in situ pumping of the SR Ca-ATPase is sufficiently high to account for the removal of Ca2+ from the Ca2+-specific sites of troponin (0.18 mmol of Ca2+-specific sites/liter of cytoplasmic H2O) and for the rate of relaxation from a tetanus at room temperature. The half-time of the return of the total 1.0 mmol of Ca2+/liter of cytoplasmic H2O released during a tetanus was 1.1 s, comparable to the slow Koff rate of Ca2+ from (carp) parvalbumin (1.0 s-1) and consistent with the hypothesis that the return of this Ca2+ to the terminal cisternae is rate-limited by the Ca2+ off-rate from parvalbumin. The return of the Mg2+ taken up by the terminal cisternae during a tetanus to resting levels was significantly slower than the time course of the Ca2+ movements, suggesting that the Mg2+ permeability of the SR in situ is low and may be transiently increased during tetanic stimulation.

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Year:  1985        PMID: 3158652

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  37 in total

1.  Molecular cloning, functional expression and tissue distribution of the cDNA encoding frog skeletal muscle calsequestrin.

Authors:  S Treves; B Vilsen; P Chiozzi; J P Andersen; F Zorzato
Journal:  Biochem J       Date:  1992-05-01       Impact factor: 3.857

2.  Effect of temperature on relaxation rate and Ca2+, Mg2+ dissociation rates from parvalbumin of frog muscle fibres.

Authors:  T T Hou; J D Johnson; J A Rall
Journal:  J Physiol       Date:  1992-04       Impact factor: 5.182

3.  Quantitation of Ca ATPase, feet and mitochondria in superfast muscle fibres from the toadfish, Opsanus tau.

Authors:  D Appelt; V Shen; C Franzini-Armstrong
Journal:  J Muscle Res Cell Motil       Date:  1991-12       Impact factor: 2.698

4.  Intracellular calcium release channels mediate their own countercurrent: the ryanodine receptor case study.

Authors:  Dirk Gillespie; Michael Fill
Journal:  Biophys J       Date:  2008-07-11       Impact factor: 4.033

5.  Sarcoplasmic reticulum K(+) (TRIC) channel does not carry essential countercurrent during Ca(2+) release.

Authors:  Tao Guo; Alma Nani; Stephen Shonts; Matthew Perryman; Haiyan Chen; Thomas Shannon; Dirk Gillespie; Michael Fill
Journal:  Biophys J       Date:  2013-09-03       Impact factor: 4.033

6.  Sarcoplasmic Reticulum Ca2+ Release Uses a Cascading Network of Intra-SR and Channel Countercurrents.

Authors:  Vilmos Zsolnay; Michael Fill; Dirk Gillespie
Journal:  Biophys J       Date:  2018-01-23       Impact factor: 4.033

7.  High resolution ultrastructural mapping of total calcium: electron spectroscopic imaging/electron energy loss spectroscopy analysis of a physically/chemically processed nerve-muscle preparation.

Authors:  F Grohovaz; M Bossi; R Pezzati; J Meldolesi; F T Tarelli
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-14       Impact factor: 11.205

8.  Phosphorus nuclear magnetic resonance studies on the effect of duration of contraction in bull-frog skeletal muscles.

Authors:  Y Kawano; M Tanokura; K Yamada
Journal:  J Physiol       Date:  1988-12       Impact factor: 5.182

9.  Ca transients in cardiac myocytes measured with a low affinity fluorescent indicator, furaptra.

Authors:  M Konishi; J R Berlin
Journal:  Biophys J       Date:  1993-04       Impact factor: 4.033

10.  Luminal Mg2+, a key factor controlling RYR2-mediated Ca2+ release: cytoplasmic and luminal regulation modeled in a tetrameric channel.

Authors:  Derek R Laver; Bonny N Honen
Journal:  J Gen Physiol       Date:  2008-10       Impact factor: 4.086

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