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Effects of Salmonella Typhimurium Infection and Ofloxacin Treatment on Glucose and Glutamine Metabolism in Caco-2/TC-7 Cells

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Specialty Pharmacology
Date 1998 Oct 31
PMID 9797231
Citations 3
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Abstract

The effects of both Salmonella typhimurium infection and 5 mM ofloxacin treatment on 2 mM glutamine and 5 mM glucose metabolism in the enterocyte-like Caco-2/TC-7 cell line were studied. These cells utilized glutamine (212.07 +/- 16.75 [mean +/- standard deviation] nmol per h per 10(6) viable cells) and, to a lesser extent, glucose (139.63 +/- 11.52 nmol per h per 10(6) viable cells). Metabolism of these substrates in Caco-2/TC-7 cells resembled that in rat, pig, or human enterocytes. Infection by S. typhimurium C53-enhanced glucose and glutamine substrate utilization by 32 and 22%, respectively and enhanced glucose and glutamine substrate oxidation by eight- and twofold, respectively. These increases in glucose and glutamine metabolism (especially glucose metabolism) were due in part to the metabolism of intracellular bacteria and/or to the activation of cellular metabolism. Substrate metabolism (especially glucose metabolism) in C53-infected cells was partially reduced by treatment with ofloxacin. It was concluded that cellular fuel metabolism is stimulated at the earliest stage of infection (3 to 4 h) and that treatment with 5 mM ofloxacin does not completely restore substrate metabolism to the levels observed in uninfected cells, possibly because this treatment does not eradicate intracellular S. typhimurium completely.

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References
1.
Tulkens P . Intracellular distribution and activity of antibiotics. Eur J Clin Microbiol Infect Dis. 1991; 10(2):100-6. DOI: 10.1007/BF01964420. View

2.
LOWRY O, ROSEBROUGH N, FARR A, RANDALL R . Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193(1):265-75. View

3.
Francis C, Starnbach M, Falkow S . Morphological and cytoskeletal changes in epithelial cells occur immediately upon interaction with Salmonella typhimurium grown under low-oxygen conditions. Mol Microbiol. 1992; 6(21):3077-87. DOI: 10.1111/j.1365-2958.1992.tb01765.x. View

4.
Morel M, Cherbuy C, Bernard F, Posho L, Blachier F, Meslin J . Metabolic characteristics of pig colonocytes after adaptation to a high fiber diet. J Nutr. 1993; 123(2):234-43. DOI: 10.1093/jn/123.2.234. View

5.
Chantret I, Rodolosse A, Barbat A, Dussaulx E, Brot-Laroche E, ZWEIBAUM A . Differential expression of sucrase-isomaltase in clones isolated from early and late passages of the cell line Caco-2: evidence for glucose-dependent negative regulation. J Cell Sci. 1994; 107 ( Pt 1):213-25. DOI: 10.1242/jcs.107.1.213. View