The location of chloride in single striated muscle fibers of the giant barnacle

1968 ◽  
Vol 46 (2) ◽  
pp. 213-219 ◽  
Author(s):  
D. C. Gayton ◽  
J. A. M. Hinke

Chloride-sensitive Ag–AgCl microelectrodes were inserted into single striated muscle fibers of the giant barnacle, Balanus nubilus, to measure the activity of Cl− in the myoplasm, (aCl)i. Chemical analysis was also carried out to determine the total concentration of Cl− in the fiber, [Cl]i. In two sets of experiments, (aCl)i was 28.8 and 22.4 mM while [Cl]i was 75.1 and 66.8 mmoles/kg fiber water respectively. The transmembrane Cl− potential, calculated from the aCl measurements in the myoplasm and the bath, was slightly less than the membrane potential. To locate the large fraction of fiber Cl− that is not free in the myoplasm, Cl− washout studies were done in constant [K]o[Cl]o product Ringer solutions in which [Cl]o was reduced to 50% and 25% of the normal concentration. Fibers which were soaked in these solutions for 30 min showed no change in (aCl)i but a large drop in [Cl]i. From the extent of this drop, it was calculated that these muscle fibers have an extracellular space of about 5% of fiber volume. Electron microscopic studies indicate that this space is comprised of large clefts and smaller tubules which penetrate deeply into the fiber.

1967 ◽  
Vol 7 (3) ◽  
pp. 499-504 ◽  
Author(s):  
BENJAMIN WALCOTT ◽  
ELLIS B. RIDGWAY

1981 ◽  
Vol 111 (3) ◽  
pp. 240-246 ◽  
Author(s):  
Jesús G. Ninomiya ◽  
Olga M. Echeverría ◽  
Gerardo H. Vázquez-Nin

1967 ◽  
Vol 33 (2) ◽  
pp. 255-263 ◽  
Author(s):  
Philip W. Brandt ◽  
Enrique Lopez ◽  
John P. Reuben ◽  
Harry Grundfest

In cross-sections of single fibers from the frog semitendinosus muscle the number of thick myofilaments per unit area (packing density) is a direct function of the sarcomere length. Our data, derived from electron microscopic studies, fit well with other data derived from in vivo, low-angle X-ray diffraction studies of whole semitendinosus muscles. The data are consistent with the assumption that the sarcomere of a fibril maintains a constant volume during changes in sarcomere length. The myofilament lattice, therefore, expands as the sarcomere shortens. Since the distance between adjacent myofilaments is an inverse square root function of sarcomere length, the interaction of the thick and the thin myofilaments during sarcomere shortening may occur over distances which increase 70 A or more. The "expanding-sarcomere, sliding-filament" model of sarcomere shortening is discussed in terms of the current concepts of muscle architecture and contraction.


2007 ◽  
Vol 11 (5) ◽  
pp. 375-381 ◽  
Author(s):  
Giuseppe Coppolino ◽  
Davide Bolignano ◽  
Sergio Parisi ◽  
Emanuele Aloisi ◽  
Adolfo Romeo ◽  
...  

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