ascorbic-acid and Mucopolysaccharidosis-I

ascorbic-acid has been researched along with Mucopolysaccharidosis-I* in 5 studies

Other Studies

5 other study(ies) available for ascorbic-acid and Mucopolysaccharidosis-I

ArticleYear
Effects of vitamins A and C on urinary excretion of acid mucopolysaccharides in the Hurler's syndrome.
    Paediatria Universitatis Tokyo, 1970, Volume: 17

    Topics: Ascorbic Acid; Child; Child, Preschool; Chromatography, Ion Exchange; Glycosaminoglycans; Heparin; Humans; Mucopolysaccharidosis I; Sulfates; Vitamin A

1970
Study of the Hurler syndrome using cell culture: definition of the biochemical phenotype and the effects of ascorbic acid on the mutant cell.
    The Journal of clinical investigation, 1968, Volume: 47, Issue:2

    Fibroblasts from patients with Hurler syndrome retain a distinctive biochemical phenotype when grown in culture which is characterized by increased synthesis of both nonsulfated and sulfated glycosaminoglycans. Ascorbic acid reinforces the phenotypic expression of the biochemical abnormality, producing not only increased synthesis of sulfated glycosaminoglycans, but selective retention of sulfated glycosaminoglycans within the cell. Although the synthesis of nonsulfated glycosaminoglycans is also increased, these compounds, particularly hyaluronic acid are not retained by the cell but are secreted into the medium. Analyses of urine from patients with Hurler syndrome show increased absolute concentrations of nonsulfated glycosaminoglycans in addition to the expected increase in sulfated glycosaminoglycans. This indicates that the biochemical phenotype as defined in cell culture is not an artifact of the experimental model but reflects the biochemical defect in the patient. Redefinition of the biochemical defect to include nonsulfated as well as sulfated glycosaminoglycans contradicts explanations of this disease which are based on a single structural gene mutation.

    Topics: Ascorbic Acid; Culture Techniques; Fibroblasts; Glycosaminoglycans; Humans; Models, Biological; Molecular Biology; Mucopolysaccharidosis I; Mutation; Phenotype; Sulfates

1968
Failure to induce scurvy by ascorbic acid depletion in a patient with Hurler's syndrome.
    Pediatrics, 1968, Volume: 42, Issue:6

    Topics: Adrenocorticotropic Hormone; Amino Acids; Ascorbic Acid; Biopsy; Bone Development; Dentition; Diet Therapy; Female; Glycosaminoglycans; Hernia, Umbilical; Humans; Hydroxyproline; Infant; Mucopolysaccharidosis I; Phenylalanine; Scurvy; Skin; Tyrosine; Wound Healing

1968
Therapeutic trials in the inborn errors. An attempt to modify Hurler's syndrome.
    Pediatrics, 1968, Volume: 42, Issue:6

    Topics: Ascorbic Acid; Diet Therapy; Female; Humans; Infant; Mucopolysaccharidosis I; Scurvy

1968
Vitamin C-induced increase of dermatan sulfate in cultured Hurler's fibroblasts.
    Science (New York, N.Y.), 1966, Aug-26, Volume: 153, Issue:3739

    In fibroblasts taken from patients witli Hurler's syndromne and grown in cultlure, dermatan sulfate constituted a larger percentage of the total sulfated glycosaminoglycans than it did in cultured fibroblasts from unaffected individuals. Moreover, the addition of ascorbic acid (vitamnin C) to the culture medium markedly increased the concentration of dermatan sulfate in the Hurler's fibroblasts but not in the normal fibroblasts. The biochemical phenotype of the Hurler's cells persisted during 28 weeks of serial culture.

    Topics: Ascorbic Acid; Fibroblasts; Glycosaminoglycans; Humans; In Vitro Techniques; Mucopolysaccharidosis I; Skin

1966