Evidence for Na Sequestration in muscle from Na Diffusion Measurements

1972 ◽  
Vol 50 (3) ◽  
pp. 228-237 ◽  
Author(s):  
J. P. Caillé ◽  
J. A. M. Hinke

Intrafiber diffusion of 22Na and 14C-sorbitol was measured along the longitudinal axis of a single muscle fiber which had been placed inside the lumen of a glass capillary at least 24 h beforehand. Compared to their diffusion in 1% agar, the self-diffusion coefficients of 22Na at 10 °C (0.438 × 10−5 cm2/s) and 14C-sorbitol (0.216 × 10−5 cm2/s) were reduced by a factor of 2 when intrafiber pH was 7.5. However, the theoretical and experimental concentration–distance profile curves only matched for 14C-sorbitol but not for 22Na. In the latter case, the experimental curves were consistently higher than the theoretical curve indicating an excess accumulation of 22Na at all x values (axis distance). This Na accumulation was found to be highly dependent on the pH inside the fiber. From pH 10.1 to 5.2, the fraction of excess Na (excess 22Na per total 22Na at a given x) decreased from 0.34 to zero. We interpret this excess Na to be a measure of the amount of myoplasmic Na which is acting as counterion for the fixed negative charge on the contractile filaments.

1973 ◽  
Vol 51 (5) ◽  
pp. 390-400 ◽  
Author(s):  
J. P. Caillé ◽  
J. A. M. Hinke

Intrafiber diffusion of 42K+, 36Cl−, and 14C-sorbitol was measured along the longitudinal axis of a single muscle fiber which had been placed inside the lumen of a glass capillary at least 24 h beforehand. The mean diffusion coefficients (× 10−5 cm2/s) in myoplasm at 10 °C and at pH 7.5 were 0.728 ± 0.008, 0.683 ± 0.006, and 0.216 ± 0.005 for K+, Cl−, and sorbitol, respectively. The K+ coefficient decreased, the Cl− coefficient increased, and the sorbitol coefficient remained unchanged as the pH of the muscle-capillary preparation was increased. By applying Wang's theory to explain diffusion in polyelectrolyte solutions (1954), we have estimated the diffusible volume (1 − ϕ) and the binding fractions (ƒK and ƒCl) of K+ and Cl− in myoplasm. From pH 5.2 to 10, ƒK varied from 0 to 0.13 and ƒCl varied from 0.13 to 0. Analysis of this K+ diffusion data along with the Na+ diffusion data from an earlier study (Can. J. Physiol. Pharmacol. 50, 228–237, 1972) leads to the prediction that myoplasm at physiological pH has a minimum binding capacity for Na+ and K+ of about 70 mmol/kg dry weight and a selectivity of 3.3 for Na+ over K+. Estimations of the diffusible volume ranged from 0.7 to 0.8, indicating that probably all the intrafiber water (74–78% by weight) is being utilized in the diffusion process.


Author(s):  
Victor P. Arkhipov ◽  
Natalia A. Kuzina ◽  
Andrei Filippov

AbstractAggregation numbers were calculated based on measurements of the self-diffusion coefficients, the effective hydrodynamic radii of micelles and aggregates of oxyethylated alkylphenols in aqueous solutions. On the assumption that the radii of spherical micelles are equal to the lengths of fully extended neonol molecules, the limiting values of aggregation numbers corresponding to spherically shaped neonol micelles were calculated. The concentration and temperature ranges under which spherical micelles of neonols are formed were determined.


Cell Reports ◽  
2017 ◽  
Vol 19 (11) ◽  
pp. 2396-2409 ◽  
Author(s):  
Marta Murgia ◽  
Luana Toniolo ◽  
Nagarjuna Nagaraj ◽  
Stefano Ciciliot ◽  
Vincenzo Vindigni ◽  
...  

1994 ◽  
Vol 17 (11) ◽  
pp. 1301-1307 ◽  
Author(s):  
Daniel Dumitru ◽  
John C. King ◽  
William van der Rijt ◽  
Dick F. Stegeman

1974 ◽  
Vol 14 (6) ◽  
pp. 915-918
Author(s):  
A. M. Sazonov ◽  
V. M. Olevskii ◽  
A. B. Porai-Koshits ◽  
V. N. Skobolev ◽  
G. A. Shmuilovich

1982 ◽  
Vol 76 (1) ◽  
pp. 12-24 ◽  
Author(s):  
A. Gydikov ◽  
P. Gatev ◽  
G.V. Dimitrov ◽  
L. Gerilovsky

2012 ◽  
Vol 1 (6) ◽  
pp. 334-346 ◽  
Author(s):  
Rafik Besbes ◽  
Noureddine Ouerfelli ◽  
Manef Abderabba ◽  
Patric Lindqvist-Reis ◽  
Habib Latrous

1986 ◽  
Vol 41 (7) ◽  
pp. 939-943 ◽  
Author(s):  
E. Hawlicka

The self-diffusion coefficients of Na+, Cl- and I- in methanol-water solutions at 35 ± 0.01 °C have been measured in their dependence on the salt molarity in the range 1 · 10-4- 1 · 10-2 mol dm -3. The ionic self-diffusion coefficients in infinitely diluted solutions have been computed. The influence of the solvent composition on the solvation of the ions is discussed. A preferential hydration of Na+, Cl- and I- ions in water-methanol mixtures has been found.


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