Enhanced glucose absorption in the rat small intestine following repeated doses of 5-fluorouracil

• Published in: Chemico-biological interactions 2005-08, Vol.155 (3), p.129-139
• Main Authors: Tomimatsu, Takashi, Horie, Toshiharu
• Format: Article
• Language: English
• Subjects: 3-O-Methylglucose - metabolism; 5-Fluorouracil; Administration, Oral; Alkaline Phosphatase - metabolism; Animals; Antimetabolites, Antineoplastic - administration & dosage; Antimetabolites, Antineoplastic - toxicity; d-Glucose; Enzyme Activation - drug effects; Fluorouracil - administration & dosage; Fluorouracil - toxicity; Glucose - metabolism; In Vitro Techniques; Intestinal absorption; Intestinal Absorption - drug effects; Intestine, Small - drug effects; Intestine, Small - metabolism; Kinetics; Male; Membrane fluidity; Membrane Fluidity - drug effects; Membrane Glycoproteins - metabolism; Methotrexate - toxicity; Microvilli - drug effects; Microvilli - metabolism; Monosaccharide Transport Proteins - metabolism; Phlorhizin - metabolism; Rats; Rats, Wistar; SGLT1; Sodium-Glucose Transporter 1; Sodium-Potassium-Exchanging ATPase - metabolism
• ISSN: 0009-2797; 1872-7786
• DOI: 10.1016/j.cbi.2005.04.001

Many studies demonstrated that 5-fluorouracil (5-FU) treatment of rodents caused the damage of small intestine, resulting in the malabsorption, while we recently found that repeated administration of 5-FU to rats increased Na +-dependent glucose absorption in the small intestine. This study investigated the cause of enhanced glucose absorption. 3- O-methyl- d-glucose (3-OMG) absorption was examined using the everted intestine technique. d-Glucose uptake, phlorizin binding, Western blot analysis and membrane fluidity were examined using small intestinal brush-border membrane vesicles (BBMV). Repeated oral administration of 5-FU to rats increased Na +-dependent 3-OMG absorption in the small intestine, while alkaline phosphatase activity in the small intestine decreased. Na +/K +-ATPase activity of 5-FU-treated rats was about three-fold higher than that of control rats. Although the amount of Na +-dependent glucose co-transporter (SGLT1) in 5-FU-treated rats decreased, the overshoot magnitude of d-glucose uptake in BBMV was not altered. Maximum binding of phlorizin in 5-FU-treated rats was 1.5-fold larger than that of control rats, but not altered the maximal rate of d-glucose absorption, Michaelis constant of d-glucose and dissociation constant of phlorizin. The membrane fluidity of 5-FU-treated rats increased. The enhanced d-glucose absorption in 5-FU-treated rats seems to occur secondarily due to the activation of Na +/K +-ATPase activity in basolateral membranes (BLM). Because the amounts of SGLT1 in 5-FU-treated rats decreased, the increase of turnover rate of SGLT1 and/or an expression of unknown Na +-dependent glucose co-transporter with high affinity for d-glucose and phlorizin sensitivity would contribute to the enhancement of d-glucose transport in 5-FU-treated rats.