Literature DB >> 8182109

Effects of diltiazem upon a rapidly exchanging calcium compartment related to repriming in frog skeletal muscle.

B A Curtis1.   

Abstract

Following spontaneous relaxation, fast skeletal muscle must first repolarize and then undergo a first-order repriming reaction before depolarization will result in maximal tension production. 45Ca exposure during repriming defined two Ca compartments during subsequent efflux, named Ca(fast) and Ca(fast). Ca(slow) had an average time constant of 112 +/- 17 min. On the basis of slow turnover and content determined by a variety of methods, I suggest Ca(slow) represents Ca within the sarcoplasmic reticulum. Ca(fast) contained 12 pmol Ca per fibre and resting exchange had a time constant of 5.1 +/- 0.4 min. A total of 12 pmol 45Ca within Ca(fast) was released during a maximal contracture. Most of the Ca released from Ca(fast) rapidly entered the extracellular space; however, 0.39 +/- 0.15 pmol Ca per fibre transferred from Ca(fast) into Ca(slow) when the muscle bundle contracted. When 1-10 microM diltiazem reduced contracture time-tension, release of Ca(fast) was reduced proportionally. When 10 microM diltiazem paralyzed excitation-contraction coupling, Ca(fast) was not released. Refilling of Ca(fast) was proportional to the extent of repriming during 45Ca exposure. Although release and refilling of Ca(fast) is related to contraction, its role in excitation-contraction coupling remains to be elucidated.

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Year:  1994        PMID: 8182109     DOI: 10.1007/bf00123832

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  22 in total

Review 1.  Na/Ca exchange and first messenger Ca in skeletal muscle excitation-contraction coupling.

Authors:  B A Curtis
Journal:  Adv Exp Med Biol       Date:  1992       Impact factor: 2.622

Review 2.  Voltage sensor of excitation-contraction coupling in skeletal muscle.

Authors:  E Ríos; G Pizarro
Journal:  Physiol Rev       Date:  1991-07       Impact factor: 37.312

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

Authors:  G Brum; R Fitts; G Pizarro; E Ríos
Journal:  J Physiol       Date:  1988-04       Impact factor: 5.182

4.  Calcium content and exchange in frog skeletal muscle.

Authors:  A C Kirby; B D Lindley; J R Picken
Journal:  J Physiol       Date:  1975-12       Impact factor: 5.182

5.  Calcium depletion in frog muscle tubules: the decline of calcium current under maintained depolarization.

Authors:  W Almers; R Fink; P T Palade
Journal:  J Physiol       Date:  1981-03       Impact factor: 5.182

6.  The distribution and kinetics of release of radiocalcium in tendon and skeletal muscle.

Authors:  A M SHANES; C P BIANCHI
Journal:  J Gen Physiol       Date:  1959-05-20       Impact factor: 4.086

7.  Sizes of components in frog skeletal muscle measured by methods of stereology.

Authors:  B A Mobley; B R Eisenberg
Journal:  J Gen Physiol       Date:  1975-07       Impact factor: 4.086

8.  Calcium influx in contracting and paralyzed frog twitch muscle fibers.

Authors:  B A Curtis; R S Eisenberg
Journal:  J Gen Physiol       Date:  1985-03       Impact factor: 4.086

9.  Contractile inactivation in frog skeletal muscle fibers. The effects of low calcium, tetracaine, dantrolene, D-600, and nifedipine.

Authors:  C Caputo; P Bolaños
Journal:  J Gen Physiol       Date:  1987-03       Impact factor: 4.086

10.  The intracellular site of calcium activaton of contraction in frog skeletal muscle.

Authors:  S Winegrad
Journal:  J Gen Physiol       Date:  1970-01       Impact factor: 4.086

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