scholarly journals Boundary plasma transport studies on TFTR. Final report, September 1990--September 1991

1991 ◽  
Author(s):  
C.S. Pitcher ◽  
P.C. Stangeby
1991 ◽  
Author(s):  
C.S. Pitcher ◽  
P.C. Stangeby

1985 ◽  
Vol 248 (3) ◽  
pp. F425-F435 ◽  
Author(s):  
M. F. Flessner ◽  
J. D. Fenstermacher ◽  
R. L. Dedrick ◽  
R. G. Blasberg

Peritoneal dialysis transport studies were carried out in anesthetized rats. Injections of [14C]EDTA were made by intravenous bolus or intraperitoneal dialysis solution, and blood and peritoneal fluid samples were collected for 1 h. After death and rapid freezing of the animal, transverse sections through the abdominal cavity were cut for quantitative macroautoradiography. The plasma-to-peritoneal transport experiments with a clinical dialysis solution resulted in essentially horizontal concentration profiles versus distance in all tissues except large intestine. Estimates of the extracellular tissue fraction were: small intestine, 0.34; large intestine, 0.28; stomach, 0.30; uterus, 0.66; liver 0.35; diaphragm, 0.16; and anterior abdominal wall, 0.15. Similar experiments with an isotonic salt solution resulted in larger (13-300%) extracellular fractions in all tissues. In contrast, peritoneal-to-plasma transport studies demonstrated decreasing concentration profiles in all visceral tissues, with the first 90% of the gradient contained in the initial 400 micron of tissue from the peritoneum. Parietal tissue gradients were less steep and had higher concentration levels deep within the tissue than visceral tissues. Computer simulations using a distributed model approach compared favorably with the experimental measurements and established the validity of this approach.


2006 ◽  
Vol 13 (6) ◽  
pp. 062301 ◽  
Author(s):  
B. A. Carreras ◽  
V. E. Lynch ◽  
B. Ph. van Milligen ◽  
R. Sánchez

2010 ◽  
Vol 12 (2) ◽  
pp. 139-143
Author(s):  
Zheng Guoyao ◽  
Feng Kaiming ◽  
Sheng Guangzhao ◽  
Pan Yudong ◽  
He Hongda

Author(s):  
A. J. Tousimis

The elemental composition of amino acids is similar to that of the major structural components of the epithelial cells of the small intestine and other tissues. Therefore, their subcellular localization and concentration measurements are not possible by x-ray microanalysis. Radioactive isotope labeling: I131-tyrosine, Se75-methionine and S35-methionine have been successfully employed in numerous absorption and transport studies. The latter two have been utilized both in vitro and vivo, with similar results in the hamster and human small intestine. Non-radioactive Selenomethionine, since its absorption/transport behavior is assumed to be the same as that of Se75- methionine and S75-methionine could serve as a compound tracer for this amino acid.


Sign in / Sign up

Export Citation Format

Share Document