The Journal of General Physiology
Cell MicroControls
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

This Article
Right arrow Full Text (PDF, 1612K)
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JGP
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hollingworth, S.
Right arrow Articles by Baylor, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hollingworth, S.
Right arrow Articles by Baylor, S. M.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*CALCIUM COMPOUNDS
*CALCIUM, ELEMENTAL
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

The Journal of General Physiology, Vol 108, 455-469, Copyright © 1996 by The Rockefeller University Press


ARTICLES

The amplitude and time course of the myoplasmic free [Ca2+] transient in fast-twitch fibers of mouse muscle

S Hollingworth, M Zhao and SM Baylor
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6085, USA.

Bundles of 10-100 fibers were dissected from the extensor digitorum longus muscle of mouse, mounted in an apparatus for optical recording, and stretched to long sarcomere length (> or = 3.6 microns). One fiber within the bundle was microinjected with furaptra, a fluorescent indicator that responds rapidly to changes in myoplasmic free [Ca2+] (delta [Ca2+]). Twitches and brief tetani were initiated by external stimulation. At myoplasmic furaptra concentrations of approximately 0.1 mM, the indicator's fluorescence signal during fiber activity (delta F/F) was well resolved. delta F/F was converted to delta [Ca2+] under the assumption that furaptra's myoplasmic dissociation constant for Ca2+ is 98 microM at 16 degrees C and 109 microM at 28 degrees C. At 16 degrees C, the peak amplitude of delta [Ca2+] during a twitch was 17.8 +/- 0.4 microM (+/-SEM; n = 8) and the half-width of delta [Ca2+] was 4.6 +/- 0.3 ms. At 28 degrees C, the peak and half-width values were 22.1 +/- 1.8 microM and 2.0 +/- 0.1 ms, respectively (n = 4). During a brief high-frequency tetanus, individual peaks of delta [Ca2+] were also well resolved and reached approximately the same amplitude that resulted from a single shock; the initial decays of delta [Ca2+] from peak slowed substantially during the tetanus. For a single twitch at 16 degrees C, the amplitude of delta [Ca2+] in fast-twitch fibers of mouse is not significantly different from that recently measured in fast- twitch fibers of frog (16.5 +/- 0.9 microM; Zhao, M., S. Hollingworth, and S.M. Baylor. 1996. Biophys. J. 70:896-916); in contrast, the half- width of delta [Ca2+] is surprisingly brief in mouse fibers, only about half that measured in frog (9.6 +/- 0.6 ms). The estimated peak rate at which Ca2+ is released from the sarcoplasmic reticulum in response to an action potential is also similar in mouse and frog, 140-150 microM/ms (16 degrees C).
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Physiol.Home page
S. Hollingworth, U. Zeiger, and S. M. Baylor
Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice
J. Physiol., November 1, 2008; 586(21): 5063 - 5075.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
L. Royer, S. Pouvreau, and E. Rios
Evolution and modulation of intracellular calcium release during long-lasting, depleting depolarization in mouse muscle
J. Physiol., October 1, 2008; 586(19): 4609 - 4629.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
S. M. Baylor and S. Hollingworth
Simulation of Ca2+ Movements within the Sarcomere of Fast-Twitch Mouse Fibers Stimulated by Action Potentials
J. Gen. Physiol., September 1, 2007; 130(3): 283 - 302.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
C. Paolini, M. Quarta, A. Nori, S. Boncompagni, M. Canato, P. Volpe, P. D. Allen, C. Reggiani, and F. Protasi
Reorganized stores and impaired calcium handling in skeletal muscle of mice lacking calsequestrin-1
J. Physiol., September 1, 2007; 583(2): 767 - 784.
[Abstract] [Full Text] [PDF]


Home page
Journals of Gerontology Series A: Biological Sciences and Medical SciencesHome page
S. Boncompagni, L. d'Amelio, S. Fulle, G. Fano, and F. Protasi
Progressive disorganization of the excitation-contraction coupling apparatus in aging human skeletal muscle as revealed by electron microscopy: a possible role in the decline of muscle performance.
J. Gerontol. A Biol. Sci. Med. Sci., October 1, 2006; 61(10): 995 - 1008.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
J. Capote, P. Bolanos, R. P. Schuhmeier, W. Melzer, and C. Caputo
Calcium transients in developing mouse skeletal muscle fibres
J. Physiol., April 15, 2005; 564(2): 451 - 464.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
D. Ursu, R. P. Schuhmeier, and W. Melzer
Voltage-controlled Ca2+ release and entry flux in isolated adult muscle fibres of the mouse
J. Physiol., January 15, 2005; 562(2): 347 - 365.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. L Dutka and G. D Lamb
Effect of low cytoplasmic [ATP] on excitation-contraction coupling in fast-twitch muscle fibres of the rat
J. Physiol., October 15, 2004; 560(2): 451 - 468.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
W. A. Macdonald and D. G. Stephenson
Effects of ADP on action potential-induced force responses in mechanically skinned rat fast-twitch fibres
J. Physiol., September 1, 2004; 559(2): 433 - 447.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
L. Csernoch, J. Zhou, M. D. Stern, G. Brum, and E. Rios
The elementary events of Ca2+ release elicited by membrane depolarization in mammalian muscle
J. Physiol., May 15, 2004; 557(1): 43 - 58.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
C. E. Woods, D. Novo, M. DiFranco, and J. L. Vergara
The action potential-evoked sarcoplasmic reticulum calcium release is impaired in mdx mouse muscle fibres
J. Physiol., May 15, 2004; 557(1): 59 - 75.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
S M Baylor and S Hollingworth
Sarcoplasmic reticulum calcium release compared in slow-twitch and fast-twitch fibres of mouse muscle
J. Physiol., August 15, 2003; 551(1): 125 - 138.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
G S Posterino and G D Lamb
Effect of sarcoplasmic reticulum Ca2+ content on action potential-induced Ca2+ release in rat skeletal muscle fibres
J. Physiol., August 15, 2003; 551(1): 219 - 237.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
G S Posterino, M A Cellini, and G D Lamb
Effects of oxidation and cytosolic redox conditions on excitation-contraction coupling in rat skeletal muscle
J. Physiol., March 15, 2003; 547(3): 807 - 823.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
S. He, D. A. Shelly, A. E. Moseley, P. F. James, J. H. James, R. J. Paul, and J. B. Lingrel
The {alpha}1- and {alpha}2-isoforms of Na-K-ATPase play different roles in skeletal muscle contractility
Am J Physiol Regulatory Integrative Comp Physiol, September 1, 2001; 281(3): R917 - R925.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
N. Kurebayashi and Y. Ogawa
Depletion of Ca2+ in the sarcoplasmic reticulum stimulates Ca2+ entry into mouse skeletal muscle fibres
J. Physiol., May 15, 2001; 533(1): 185 - 199.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
N. Shirokova, A. Gonzalez, W. G. Kirsch, E. Rios, G. Pizarro, M. D. Stern, and H. Cheng
Calcium Sparks: Release Packets of Uncertain Origin and Fundamental Role
J. Gen. Physiol., March 1, 1999; 113(3): 377 - 384.
[Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
B. Schwaller, J. Dick, G. Dhoot, S. Carroll, G. Vrbova, P. Nicotera, D. Pette, A. Wyss, H. Bluethmann, W. Hunziker, et al.
Prolonged contraction-relaxation cycle of fast-twitch muscles in parvalbumin knockout mice
Am J Physiol Cell Physiol, February 1, 1999; 276(2): C395 - C403.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
N. Shirokova, J. Garcia, and E. Rios
Local calcium release in mammalian skeletal muscle
J. Physiol., October 15, 1998; 512(2): 377 - 384.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
S.M. Baylor and S. Hollingworth
Model of Sarcomeric Ca2+ Movements, Including ATP Ca2+ Binding and Diffusion, during Activation of Frog Skeletal Muscle
J. Gen. Physiol., September 1, 1998; 112(3): 297 - 316.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
V. A. Golovina and M. P. Blaustein
Spatially and Functionally Distinct Ca2+ Stores in Sarcoplasmic and Endoplasmic Reticulum
Science, March 14, 1997; 275(5306): 1643 - 1648.
[Abstract] [Full Text]



  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents