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, glucose, insulin, and amino acids
in islets of Langerhans cultured in a microgravity model
system
1 Diabetes Research Laboratory, Program in Nutrition and Biochemistry and 2 Program in Physiology, Division of Basic Medical Sciences, Mercer University School of Medicine, Macon, Georgia 31207; 3 National Space Biomedical Research Institute, Houston 77030; 4 Nutritional Biochemistry Laboratory and 5 Laboratory for Human Immune Function and Signal Transduction, Life Sciences Research Laboratories, National Aeronautics and Space Administration Lyndon B. Johnson Space Center, Houston, Texas 77058
The present
studies were designed to determine effects of a microgravity model
system upon lipopolysaccharide (LPS)-stimulated tumor necrosis
factor-
(TNF-
) activity and indexes of insulin and fuel
homeostasis of pancreatic islets of Langerhans. Islets (1,726 ± 117, 150 islet equivalent units) from Wistar-Furth rats were treated as
1) high aspect ratio vessel (HARV) cell culture, 2) HARV plus LPS, 3) static culture, and
4) static culture plus LPS. TNF-
(L929 cytotoxicity
assay) was significantly increased in LPS-induced HARV and static
cultures; yet the increase was more pronounced in the static culture
group (P < 0.05). A decrease in insulin concentration
was demonstrated in the LPS-stimulated HARV culture (P < 0.05). We observed a greater glucose concentration and increased
disappearance of arginine in islets cultured in HARVs. Although
nitrogenous compound analysis indicated a ubiquitous reliance on
glutamine in all experimental groups, arginine was converted to
ornithine at a twofold greater rate in the islets cultured in the HARV
microgravity model system (P < 0.05). These studies
demonstrate alterations in LPS-induced TNF-
production of pancreatic
islets of Langerhans, favoring a lesser TNF activity in the HARV. These
alterations in fuel homeostasis may be promulgated by gravity-averaged
cell culture methods or by three-dimensional cell assembly.
tumor necrosis factor-
; cytokines; diabetes; amino acids
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