J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Vol 357 pp 185-201
Copyright © 1984 by The Physiological Society
This Article
Right arrow Full Text (PDF)
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bond, M
Right arrow Articles by Somlyo, A V
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bond, M
Right arrow Articles by Somlyo, A V

Total cytoplasmic calcium in relaxed and maximally contracted rabbit portal vein smooth muscle.

M Bond, H Shuman, A P Somlyo and A V Somlyo

The concentration of total cytoplasmic Ca in vascular smooth muscle was measured by electron probe microanalysis of strips of rabbit portal anterior mesenteric vein that were rapidly frozen either when relaxed or during a maintained (30 min) maximal contraction stimulated with high K and noradrenaline. Strips were also frozen and analysed after incubation in Ca-free, high-Mg2+ solution. Probe diameters of 0.1-0.2 micron and 1.0-1.5 micron were used to measure, respectively, cytoplasmic and cellular (including stored) Ca. There was a highly significant increase (P less than 0.0005) in cytoplasmic Ca of 1.0 +/- 0.2 (S.D.) mmol Ca/kg dry wt. from 0.8 +/- 0.2 (S.E. of mean) mmol/kg dry wt. (n = 262 spectra, six animals) to 1.8 +/- 0.2 (S.E. of mean) mmol Ca/kg dry wt. (n = 296 spectra, six animals), during maximal contraction. This increase is greater than can be accounted for by Ca binding to calmodulin and to myosin, suggesting the presence of other Ca-binding proteins in smooth muscle. A small amount (0.4-0.6 mmol/kg dry wt.) of cytoplasmic Ca remained after incubation in Ca-free, high-Mg2+ EGTA solution. This tightly bound, cytoplasmic Ca is insufficient to account for the total amount of divalent cation known to be bound to F-actin. We conclude that Mg is the major inexchangeably bound cation in F-actin in smooth as in striated muscle. In the contracted muscles, the cellular Ca concentration, measured with the large probes that include Ca stored in the sarcoplasmic reticulum (s.r.), was 3.2 +/- 0.3 (S.E. of mean) mmol Ca/kg dry wt. (n = 93), significantly higher than the cytoplasmic Ca concentration measured with small probes. This value of cellular Ca is probably an underestimate, as the large-diameter probes did not cover all of the peripheral s.r. The cellular Ca (measured with large probes) was highest in the contracted and lower in the relaxed tissue, and was significantly reduced in the muscles incubated in Ca-free solution. In contracted muscle, cytoplasmic Mg significantly decreased and mitochondrial Mg increased. In 0 Ca, high-Mg2+ solution, the cytoplasmic Mg increased significantly. Mitochondrial Ca did not significantly change during a maintained contraction, but was significantly lower (0.0 +/- 0.2 (S.E. of mean) mmol Ca/kg dry wt.) after incubation in Ca-free, high-Mg2+ solution than in the relaxed tissue (1.6 +/- 0.2 mmol Ca/kg dry wt.) in normal Ca-containing solution.




This article has been cited by other articles:


Home page
Biophys. JHome page
M. Tashiro, P. Tursun, T. Miyazaki, M. Watanabe, and M. Konishi
Effects of Intracellular and Extracellular Concentrations of Ca2+, K+, and Cl- on the Na+-Dependent Mg2+ Efflux in Rat Ventricular Myocytes
Biophys. J., July 1, 2006; 91(1): 244 - 254.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
M. Watanabe, M. Konishi, I. Ohkido, and S. Matsufuji
Enhanced sodium-dependent extrusion of magnesium in mutant cells established from a mouse renal tubular cell line
Am J Physiol Renal Physiol, October 1, 2005; 289(4): F742 - F748.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
P. Tursun, M. Tashiro, and M. Konishi
Modulation of Mg2+ Efflux from Rat Ventricular Myocytes Studied with the Fluorescent Indicator Furaptra
Biophys. J., March 1, 2005; 88(3): 1911 - 1924.
[Abstract] [Full Text] [PDF]


Home page
Pharmacol. Rev.Home page
R. Laporte, A. Hui, and I. Laher
Pharmacological Modulation of Sarcoplasmic Reticulum Function in Smooth Muscle
Pharmacol. Rev., December 1, 2004; 56(4): 439 - 513.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
R. ZhuGe, K. E. Fogarty, S. P. Baker, J. G. McCarron, R. A. Tuft, L. M. Lifshitz, and J. V. Walsh Jr.
Ca2+ spark sites in smooth muscle cells are numerous and differ in number of ryanodine receptors, large-conductance K+ channels, and coupling ratio between them
Am J Physiol Cell Physiol, December 1, 2004; 287(6): C1577 - C1588.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
R. ZhuGe, K. E. Fogarty, R. A. Tuft, and J. V. Walsh Jr
Spontaneous Transient Outward Currents Arise from Microdomains Where BK Channels Are Exposed to a Mean Ca2+ Concentration on the Order of 10 {micro}M during a Ca2+ Spark
J. Gen. Physiol., June 10, 2002; 120(1): 15 - 28.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
M. Tashiro and M. Konishi
Sodium gradient-dependent transport of magnesium in rat ventricular myocytes
Am J Physiol Cell Physiol, December 1, 2000; 279(6): C1955 - C1962.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
R. E. Lesh, A. P. Somlyo, G. K. Owens, and A. V. Somlyo
Reversible Permeabilization : A Novel Technique for the Intracellular Introduction of Antisense Oligodeoxynucleotides Into Intact Smooth Muscle
Circ. Res., August 1, 1995; 77(2): 220 - 230.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1984 The Physiological Society.