Glycogen Metabolism in Smooth Muscle

Author(s):  
Theodore G. Sotiroudis ◽  
Stathis Nikolaropoulos ◽  
Athanasios E. Evangelopoulos
1989 ◽  
Vol 257 (4) ◽  
pp. C736-C742 ◽  
Author(s):  
R. M. Lynch ◽  
C. P. Kuettner ◽  
R. J. Paul

To study the regulation of glycogen utilization in vascular smooth muscle, we measured the content of glycogen and glucose 6-phosphate and the activity of the glycogen phosphorylase and glycogen debrancher enzymes in porcine carotid artery. During active contraction, the rates of glycogen phosphorylase and glycogenolysis were as high as expected. Despite this, glycogen content did not decrease to less than approximately 50% of control levels even after sustained contractions. The activity of glycogen debrancher enzyme was found to be limiting glycogen utilization at this point. Although glycogenolysis is closely coordinated with increases in oxidative metabolism concomitant with active contraction, the maximal level of tension obtained after stimulation was not substantially reduced under conditions where glycogen debrancher enzyme was limiting glycogen utilization. On the other hand, the rate of tension generation was increased in these tissues. Thus glycogen utilization is not necessary for maximal force generation per se, but may influence other muscle contractile properties. Finally, during steady-state tension maintenance, glycogen utilization is likely to be regulated by the intracellular concentrations of metabolic intermediates (glucose, glucose 6-phosphate), as it is in skeletal muscle.


1995 ◽  
Vol 32 (5) ◽  
pp. 293-300 ◽  
Author(s):  
Christopher D. Hardin ◽  
Martin J. Kushmerick ◽  
Tina M. Roberts

1957 ◽  
Vol 38 (3-4) ◽  
pp. 237-254 ◽  
Author(s):  
LENNART LUNDHOLM ◽  
ELLA MOHME-LUNDHOLM

Author(s):  
Theodore G. Sotiroudis ◽  
Stathis Nikolaropoulos ◽  
Athanasios E. Evangelopoulos

1986 ◽  
Vol 134 (2) ◽  
pp. 484-491 ◽  
Author(s):  
Maria Spatz ◽  
Bogomir B. Mrsulja ◽  
Barbara Wroblewska ◽  
Nancy Merkel ◽  
Joliet Bembry

Author(s):  
T. M. Murad ◽  
H. A. I. Newman ◽  
K. F. Kern

The origin of lipid containing cells in atheromatous lesion has been disputed. Geer in his study on atheromatous lesions of rabbit aorta, suggested that the early lesion is composed mainly of lipid-laden macrophages and the later lesion has a mixed population of macrophages and smooth muscle cells. Parker on the other hand, was able to show evidence that the rabbit lesion is primarily composed of lipid-laden cells of smooth muscle origin. The above studies and many others were done on an intact lesion without any attempt of cellular isolation previous to their ultrastructural studies. Cell isolation procedures have been established for atherosclerotic lesions through collagenase and elastase digestion Therefore this procedure can be utilized to identify the cells involved in rabbit atheroma.


Author(s):  
A. V. Somlyo ◽  
H. Shuman ◽  
A. P. Somlyo

Electron probe analysis of frozen dried cryosections of frog skeletal muscle, rabbit vascular smooth muscle and of isolated, hyperpermeab1 e rabbit cardiac myocytes has been used to determine the composition of the cytoplasm and organelles in the resting state as well as during contraction. The concentration of elements within the organelles reflects the permeabilities of the organelle membranes to the cytoplasmic ions as well as binding sites. The measurements of [Ca] in the sarcoplasmic reticulum (SR) and mitochondria at rest and during contraction, have direct bearing on their role as release and/or storage sites for Ca in situ.


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