Vitamin A protects the small intestine from methotrexate-induced damage in rats

• Published in: The Journal of pharmacology and experimental therapeutics Vol. 253; no. 3; pp. 1278 - 1284
• Main Authors: TSURUI, K, KOSAKAI, Y, HORIE, T, AWAZU, S
• Format: Journal Article
• Language: English
• Published: Bethesda, MD American Society for Pharmacology and Experimental Therapeutics 01.06.1990
• Subjects: Administration, Oral; Animals; Biological and medical sciences; Cell Membrane Permeability - drug effects; Drug Interactions; Drug toxicity and drugs side effects treatment; Intestinal Absorption - drug effects; Intestine, Small - drug effects; Intestine, Small - pathology; Male; Medical sciences; Methotrexate - blood; Methotrexate - pharmacokinetics; Methotrexate - toxicity; Pharmacology. Drug treatments; Rats; Rats, Inbred Strains; Toxicity: digestive system; Vitamin A - therapeutic use; Antineoplastic agent; Drug combination; Rat; Toxicity; Rodentia; Vitamin; Oral administration; Cytotoxicity; Small intestine; Retinol; Antifolate; Prevention; Vertebrata; Chemotherapy; Mammalia; Treatment; Animal; Digestive diseases; Drug interaction; Mucosa disease
• ISSN: 0022-3565; 1521-0103

A protective effect of vitamin A (VA) against cytotoxic antitumor drug-induced damage of rat small intestine was found. Oral administration of methotrexate (MTX) for the small intestinal mucosa of rats resulted in a severe histological change, whereas rats coadministered VA with MTX showed a histological status similar to that of control rats. The p.o. administration of MTX led to a decrease in the amounts of membrane proteins and lipids in rat small intestine and its brush border membrane. When administered p.o. with VA, this decrease failed to occur. The brush border membrane of MTX plus VA-treated rats, when monitored by the fluorescence of cationic safranin O and anionic 8-anilino-1-naphthalenesulfonic acid, was found to resemble that from control rats rather than that from MTX-treated rats. The in vitro permeation of MTX in the small intestine of MTX plus VA-treated rats was enhanced, in contrast with the decrease noted for MTX-treated rats. However, that of untreated rats was not affected by the presence of VA. Thus, VA is unlikely to affect the transport process of MTX directly. When administered p.o. with VA, MTX was absorbed effectively to the same or a slightly greater extent than when administered by itself. Consequently, it has been shown histologically, biochemically, physicochemically and physiologically that VA protects the small intestine from the damage induced by MTX.