Literature DB >> 6976426

Calcium transients in normal and denervated slow muscle fibres of the frog.

R Miledi, I Parker, G Schalow.   

Abstract

1. Intracellular changes in free Ca2+ concentration were recorded from slow muscle fibres in the pyriformis muscle of Rana temporaria, using the dye arsenazo III. Fibres were voltage clamped, and arsenazo signals were recorded in response to depolarizing pulses. 2. The size of the arsenazo response to depolarizing pulses of 100 msec duration was a sigmoid function of membrane potential over the range -45 to 0 mV, and remained constant with further depolarizations up to +100 mV. 3. The peak size of the arsenazo signal to supramaximal depolarizations increased with increasing pulse length. The initial rising phase during a pulse was much slower than in twitch fibres, and this phase was followed by an even slower rise. Following short pulses the decay of the response was exponential, with a time constant of about 1.4 sec, while after long pulses the decline became much slower. 4. Decreasing free Ca2+ concentration in the bathing medium to very low levels, using EGTA , did not affect the responses to short (100 msec) depolarizations. 5. Slow fibres bathed in Ringer's solution containing 12 mM-Ca2+ showed a well maintained arsenazo response to supramaximal depolarizations lasting over 1 min. Reduction of external Ca2+ to 1.8 and (nominally) 0 mM caused the response to become progressively more transient. 6. After denervation, slow fibres developed action potentials, but non of the parameters of the arsenazo response was significantly changed. During the early phase of reinnervation by a mixed nerve, when fast conduction axons begin to innervate slow fibres, the ability to give a maintained response during long depolarizations was reduced. 7. It is concluded that intracellular Ca2+ transients in slow muscle fibres are probably generated by a similar mechanism as in twitch fibres and entry of external Ca2+ is not an appreciable factor. The slow time course of the transients may be important in determining the time courses of tension development and relaxation.

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Year:  1981        PMID: 6976426      PMCID: PMC1245485          DOI: 10.1113/jphysiol.1981.sp013858

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


  28 in total

1.  The electrical properties of the slow muscle fibre membrane.

Authors:  W BURKE; B L GINSBORG
Journal:  J Physiol       Date:  1956-06-28       Impact factor: 5.182

Review 2.  Vertebrate slow muscle fibers.

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Journal:  Physiol Rev       Date:  1970-01       Impact factor: 37.312

Review 3.  Muscle.

Authors:  L D Peachey
Journal:  Annu Rev Physiol       Date:  1968       Impact factor: 19.318

4.  The effect o f calcium on contraction and conductance thresholds in frog skeletal muscle.

Authors:  L L Costantin
Journal:  J Physiol       Date:  1968-03       Impact factor: 5.182

5.  Neural control of contracture in slow muscle fibres of the frog.

Authors:  R Elul; R Miledi; E Stefani
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6.  The volume of the T-system and its association with the sarcoplasmic reticulum in slow muscle fibres of the frog.

Authors:  F W Flitney
Journal:  J Physiol       Date:  1971-08       Impact factor: 5.182

7.  Contractures of single slow muscle fibres of Xenopus laevis elicited by potassium, acetylcholine or choline.

Authors:  J Lännergren
Journal:  Acta Physiol Scand       Date:  1967-04

8.  Effect of a "fast" nerve on "slow" muscle fibres in the frog.

Authors:  R Miledi; P Orkand
Journal:  Nature       Date:  1966-02-12       Impact factor: 49.962

9.  A study of synaptic transmission in the absence of nerve impulses.

Authors:  B Katz; R Miledi
Journal:  J Physiol       Date:  1967-09       Impact factor: 5.182

10.  Calcium activation of frog slow muscle fibres.

Authors:  L L Costantin; R J Podolsky; L W Tice
Journal:  J Physiol       Date:  1967-01       Impact factor: 5.182

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  13 in total

1.  Calcium action potentials in innervated and denervated rat muscle fibres.

Authors:  O Delbono; B A Kotsias
Journal:  Pflugers Arch       Date:  1991-04       Impact factor: 3.657

2.  Skeletal muscle Ca2+ channels.

Authors:  A J Avila-Sakar; G Cota; R Gamboa-Aldeco; J Garcia; M Huerta; J Muñiz; E Stefani
Journal:  J Muscle Res Cell Motil       Date:  1986-08       Impact factor: 2.698

3.  Calcium action potentials and calcium currents in tonic muscle fibres of the frog (Rana pipiens).

Authors:  M Huerta; E Stefani
Journal:  J Physiol       Date:  1986-03       Impact factor: 5.182

4.  Calcium transients in single mammalian skeletal muscle fibres.

Authors:  O Delbono; E Stefani
Journal:  J Physiol       Date:  1993-04       Impact factor: 5.182

5.  Stoichiometries of arsenazo III-Ca complexes.

Authors:  P Palade; J Vergara
Journal:  Biophys J       Date:  1983-09       Impact factor: 4.033

6.  Slow amphibian muscle fibres become less sensitive to Ca2+ with increasing sarcomere length.

Authors:  D G Stephenson; D A Williams
Journal:  Pflugers Arch       Date:  1983-05       Impact factor: 3.657

7.  Aequorin-calcium transients in frog twitch muscle fibres.

Authors:  F Eusebi; R Miledi; T Takahashi
Journal:  J Physiol       Date:  1983-07       Impact factor: 5.182

8.  The effect of D600 on potassium contractures of slow muscle fibres of Rana temporaria.

Authors:  H Schmidt; M Siebler; P Krippeit-Drews
Journal:  Pflugers Arch       Date:  1988-09       Impact factor: 3.657

9.  Calcium transients evoked by action potentials in frog twitch muscle fibres.

Authors:  R Miledi; I Parker; P H Zhu
Journal:  J Physiol       Date:  1982-12       Impact factor: 5.182

10.  Calcium transients in frog skeletal muscle fibres following conditioning stimuli.

Authors:  R Miledi; I Parker; P H Zhu
Journal:  J Physiol       Date:  1983-06       Impact factor: 5.182

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