scholarly journals Sepsis Increases the Plasma Membrane Content of α1 and α2 Isoforms of Na+-K+ Adenosine Triphosphatase in Rat Skeletal Muscle

2001 ◽  
Vol 136 (1) ◽  
pp. 95 ◽  
Author(s):  
Naoshi Shimoda
1993 ◽  
Vol 265 (6) ◽  
pp. C1716-C1722 ◽  
Author(s):  
A. Marette ◽  
J. Krischer ◽  
L. Lavoie ◽  
C. Ackerley ◽  
J. L. Carpentier ◽  
...  

The cellular localization of the alpha 2-subunit of the Na(+)-K(+)-ATPase was defined by immunoelectron microscopy, and the effect of insulin on the amount of alpha 2-immunoreactive subunits on the cell surface was quantitated. Two protocols were used for tissue fixation and immunolocalization. Protocol 1 was characterized by fixation with 2% paraformaldehyde, use of a monoclonal antibody, and detection with 3-nm-diameter gold-labeled Fab fragments or 10-nm gold-labeled immunoglobulin G. Protocol 2 was characterized by fixation with 4% paraformaldehyde plus 0.1% glutaraldehyde, use of a polyclonal antibody, and detection with 10-nm gold-labeled protein A. In control muscle, the alpha 2-subunit of the Na(+)-K(+)-ATPase was present at the plasma membrane and in intracellular tubular and vesicular structures located in subsarcolemmal and triadic regions. Acute insulin stimulation increased the number of immunolabeled alpha 2-subunits in the plasma membrane after both fixation protocols. The gain in the plasma membrane ranged from 1.5- to 3.7-fold and was significant at the level of P < 0.005. These results provide morphological quantitative evidence that the alpha 2-subunit of the Na(+)-K(+)-ATPase is present both at the plasma membrane and intracellularly in mammalian skeletal muscle and that insulin acutely increases its abundance in the muscle surface.


FEBS Letters ◽  
1988 ◽  
Vol 238 (2) ◽  
pp. 235-239 ◽  
Author(s):  
Michael F. Hirshman ◽  
Harriet Wallberg-Henriksson ◽  
Lawrence J. Wardzala ◽  
Elizabeth D. Horton ◽  
Edward S. Horton

1985 ◽  
Vol 41 (11) ◽  
pp. 1396-1398 ◽  
Author(s):  
A. Shah ◽  
F. Nagao ◽  
V. Sahgal ◽  
H. Singh

2012 ◽  
Vol 302 (2) ◽  
pp. E183-E189 ◽  
Author(s):  
Nicolette S. Bradley ◽  
Laelie A. Snook ◽  
Swati S. Jain ◽  
George J. F. Heigenhauser ◽  
Arend Bonen ◽  
...  

Fatty acid transport proteins are present on the plasma membrane and are involved in the uptake of long-chain fatty acids into skeletal muscle. The present study determined whether acute endurance exercise increased the plasma membrane content of fatty acid transport proteins in rat and human skeletal muscle and whether the increase was accompanied by an increase in long-chain fatty acid transport in rat skeletal muscle. Sixteen subjects cycled for 120 min at ∼60 ± 2% V̇o2 peak. Two skeletal muscle biopsies were taken at rest and again following cycling. In a parallel study, eight Sprague-Dawley rats ran for 120 min at 20 m/min, whereas eight rats acted as nonrunning controls. Giant sarcolemmal vesicles were prepared, and protein content of FAT/CD36 and FABPpm was measured in human and rat vesicles and whole muscle homogenate. Palmitate uptake was measured in the rat vesicles. In human muscle, plasma membrane FAT/CD36 and FABPpm protein contents increased 75 and 20%, respectively, following 120 min of exercise. In rat muscle, plasma membrane FAT/CD36 and FABPpm increased 20 and 30%, respectively, and correlated with a 30% increase in palmitate transport following 120 min of running. These data suggest that the translocation of FAT/CD36 and FABPpm to the plasma membrane in rat skeletal muscle is related to the increase in fatty acid transport and oxidation that occurs with endurance running. This study is also the first to demonstrate that endurance cycling induces an increase in plasma membrane FAT/CD36 and FABPpm content in human skeletal muscle, which is predicted to increase fatty acid transport.


2000 ◽  
Vol 267 (7) ◽  
pp. 1985-1994 ◽  
Author(s):  
Simona Berardi ◽  
Bruno Stieger ◽  
Bruno Hagenbuch ◽  
Ernesto Carafoli ◽  
Stephan Krähenbühl

Sign in / Sign up

Export Citation Format

Share Document