Vitamin C: update on physiology and pharmacology

被引:329
作者
Mandl, J. [1 ,2 ]
Szarka, A. [2 ,3 ]
Banhegyi, G. [1 ,2 ]
机构
[1] Semmelweis Univ Budapest, Dept Med Chem & Mol Biol & Patobiochem, H-1444 Budapest, Hungary
[2] Hungarian Acad Sci, Pathobiochem Res Grp, Budapest, Hungary
[3] Budapest Univ Technol & Econ, Biochem & Mol Biol Lab, Dept Appl Biotechnol & Food Sci, H-1117 Budapest, Hungary
关键词
vitamin C; ascorbate; dehydroascorbic acid; L-gulonolactone-oxidase; antioxidant; pro-oxidant; mitochondrium; endoplasmic reticulum; redox; scurvy; L-ASCORBIC-ACID; GLYPICAN-1; HEPARAN-SULFATE; GAMMA-LACTONE OXIDASE; LIVER ENDOPLASMIC-RETICULUM; ISOLATED MURINE HEPATOCYTES; DOMAIN-CONTAINING PROTEINS; ASPARTYL BETA-HYDROXYLASE; ELECTRON-TRANSPORT CHAIN; MITOCHONDRIAL-DNA DAMAGE; COMPLEX-III DEFICIENCY;
D O I
10.1111/j.1476-5381.2009.00282.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although ascorbic acid is an important water-soluble antioxidant and enzyme cofactor in plants and animals, humans and some other species do not synthesize ascorbate due to the lack of the enzyme catalyzing the final step of the biosynthetic pathway, and for them it has become a vitamin. This review focuses on the role of ascorbate in various hydroxylation reactions and in the redox homeostasis of subcellular compartments including mitochondria and endoplasmic reticulum. Recently discovered functions of ascorbate in nucleic acid and histone dealkylation and proteoglycan deglycanation are also summarized. These new findings might delineate a role for ascorbate in the modulation of both pro- and anti-carcinogenic mechanisms. Recent advances and perspectives in therapeutic applications are also reviewed. On the basis of new and earlier observations, the advantages of the lost ability to synthesize ascorbate are pondered. The increasing knowledge of the functions of ascorbate and of its molecular sites of action can mechanistically substantiate a place for ascorbate in the treatment of various diseases.
引用
收藏
页码:1097 / 1110
页数:14
相关论文
共 184 条
  • [1] Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA
    Aas, PA
    Otterlei, M
    Falnes, PO
    Vågbo, CB
    Skorpen, F
    Akbari, M
    Sundheim, O
    Bjorås, M
    Slupphaug, G
    Seeberg, E
    Krokan, HE
    [J]. NATURE, 2003, 421 (6925) : 859 - 863
  • [2] A novel assay for the evaluation of the prooxidant-antioxidant balance, before and after antioxidant vitamin administration in type II diabetes patients
    Alamdari, Daryoush Hamidi
    Paletas, Konstantinos
    Pegiou, Theodosia
    Sarigianni, Maria
    Befani, Christina
    Koliakos, George
    [J]. CLINICAL BIOCHEMISTRY, 2007, 40 (3-4) : 248 - 254
  • [3] URIC-ACID PROVIDES AN ANTIOXIDANT DEFENSE IN HUMANS AGAINST OXIDANT-CAUSED AND RADICAL-CAUSED AGING AND CANCER - A HYPOTHESIS
    AMES, BN
    CATHCART, R
    SCHWIERS, E
    HOCHSTEIN, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (11): : 6858 - 6862
  • [4] [Anonymous], 1753, A Treatise of the scurvy in three parts
  • [5] TREATMENT OF MITOCHONDRIAL MYOPATHY DUE TO COMPLEX-III DEFICIENCY WITH VITAMINS K3 AND C - A P-31-NMR FOLLOW-UP-STUDY
    ARGOV, Z
    BANK, WJ
    MARIS, J
    ELEFF, S
    KENNAWAY, NG
    OLSON, RE
    CHANCE, B
    [J]. ANNALS OF NEUROLOGY, 1986, 19 (06) : 598 - 602
  • [6] Ascorbate and environmental stress
    Bánhegyi, G
    Braun, L
    Csala, M
    Puskás, F
    Somogyi, A
    Kardon, T
    Mandl, J
    [J]. STRESS OF LIFE: FROM MOLECULES TO MAN, 1998, 851 : 292 - 303
  • [7] Dehydroascorbate and ascorbate transport in rat liver microsomal vesicles
    Bánhegyi, G
    Marcolongo, P
    Puskás, F
    Fulceri, R
    Mandl, J
    Benedetti, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (05) : 2758 - 2762
  • [8] Ascorbate synthesis-dependent glutathione consumption in mouse liver
    Banhegyi, G
    Csala, M
    Braun, L
    Garzo, T
    Mandl, J
    [J]. FEBS LETTERS, 1996, 381 (1-2) : 39 - 41
  • [9] Role of ascorbate in oxidative protein folding (Reprinted from Thiol Metabolism and Redox Regulation of Cellular Functions)
    Bánhegyi, G
    Csala, M
    Szarka, A
    Varsányi, M
    Benedetti, A
    Mandl, J
    [J]. BIOFACTORS, 2003, 17 (1-4) : 37 - 46
  • [10] GLYCOGENOLYSIS - AND NOT GLUCONEOGENESIS - IS THE SOURCE OF UDP-GLUCURONIC ACID FOR GLUCURONIDATION
    BANHEGYI, G
    GARZO, T
    ANTONI, F
    MANDL, J
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 967 (03) : 429 - 435