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Requirement for ascorbic acid in a rat mutant unable to synthesize ascorbic acid.

Abstract
The activities of several enzymes involved in hepatic ascorbic acid synthesis and the requirement of dietary ascorbic acid were investigated in the OD (osteogenic disorder) rat, which has a hereditary defect in ascorbic acid-synthesizing ability. No activity of hepatic L-gulonolactone oxidase was detected in OD rats. However, OD rats maintained the normal activities of hepatic UDPglucose dehydrogenase, UDPglucuronyl transferase and beta-glucuronidase. Hemorrhage in muscle and leg joints, lower hepatic content of cytochrome P-450 and lower activities of hepatic drug-metabolizing enzymes, higher serum and adrenal levels of corticosterone and lower urinary excretion of hydroxyproline were observed in ascorbic acid-deficient OD rats than in OD rats fed 300 mg ascorbic acid/kilogram diet. Consequently, we conclude that OD rats cannot synthesize ascorbic acid because of the lack of activity of hepatic L-gulonolactone oxidase and that the dietary addition of about 300 mg ascorbic acid (per kilogram diet) is enough to prevent signs of vitamin C deficiency and to achieve maximum growth, and that more than 300 mg ascorbic acid per kilogram diet may be required for the maximum activity of hepatic drug-metabolizing enzymes.
AuthorsF Horio, K Ozaki, A Yoshida, S Makino, Y Hayashi
JournalThe Journal of nutrition (J Nutr) Vol. 115 Issue 12 Pg. 1630-40 (Dec 1985) ISSN: 0022-3166 [Print] United States
PMID4067654 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Cytochrome P-450 Enzyme System
  • Ascorbic Acid
  • Hydroxyproline
  • Corticosterone
Topics
  • Adrenal Glands (metabolism)
  • Animals
  • Ascorbic Acid (administration & dosage, biosynthesis, physiology)
  • Body Weight (drug effects)
  • Corticosterone (blood, metabolism)
  • Cytochrome P-450 Enzyme System (metabolism)
  • Diet
  • Hydroxyproline (urine)
  • Liver (enzymology, metabolism)
  • Nutritional Requirements
  • Organ Size (drug effects)
  • Rats
  • Rats, Mutant Strains
  • Spleen (metabolism)

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