Mitochondrial function and toxicity: Role of B vitamins on the one-carbon transfer pathways

被引:170
作者
Depeint, Flore
Bruce, W. Robert
Shangari, Nandita
Mehta, Rhea
O'Brien, Peter J.
机构
[1] Univ Toronto, Dept Pharmaceut Sci, Toronto, ON, Canada
[2] Univ Toronto, Dept Nutrit Sci, Toronto, ON, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
folate; pyridoxal; cobalamin; choline; mitochondrial toxicity; methyl transfer;
D O I
10.1016/j.cbi.2006.05.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The B vitamins are water-soluble vitamins that are required as coenzymes for reactions essential for cellular function. This review focuses on the essential role of vitamins in maintaining the one-carbon transfer cycles. Folate and choline are believed to be central methyl donors required for mitochondrial protein and nucleic acid synthesis through their active forms, 5-methyltetrahydrofolate and betaine, respectively. Cobalamin (13 12) may assist methyltetrahydrofolate in the synthesis of methionine, a cysteine source for glutathione biosynthesis. Pyridoxal, pyridoxine and pyridoxamine (136) seem to be involved in the regeneration of tetrahydrofolate into the active methyl-bearing form and in glutathione biosynthesis from homocysteine. Other roles of these vitamins that are relevant to mitochondrial functions will also be discussed. However these roles for B vitamins in cell function are mostly theoretically based and still require verification at the cellular level. For instance it is still not known what B vitamins are depleted by xenobiotic toxins or which cellular targets, metabolic pathways or molecular toxic mechanisms are prevented by B vitamins. This review covers the cur-rent state of knowledge and suggests where this research field is heading so as to better understand the role vitamin Bs play in cellular function and intermediary metabolism as well as molecular, cellular and clinical consequences of vitamin deficiency. The current experimental and clinical evidence that supplementation alleviates deficiency symptoms as well as the effectiveness of vitamins as antioxidants will also be reviewed. (c) 2006 Published by Elsevier Ireland Ltd.
引用
收藏
页码:113 / 132
页数:20
相关论文
共 124 条
[21]  
CHANARIN I, 1974, LANCET, V1, P1251
[22]   Postnatal cerebellar defects in mice deficient in methylenetetrahydrofolate reductase [J].
Chen, ZT ;
Schwahn, BC ;
Wu, Q ;
He, XY ;
Rozen, R .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2005, 23 (05) :465-474
[23]   Interaction between pyridoxal kinase and Pyridoxal-5-phosphate-dependent enzymes [J].
Cheung, PY ;
Fong, CC ;
Ng, KT ;
Lam, WC ;
Leung, YC ;
Tsang, CW ;
Yang, MS ;
Wong, MS .
JOURNAL OF BIOCHEMISTRY, 2003, 134 (05) :731-738
[24]   Abnormal vitamin B6 status is associated with severity of symptoms in patients with rheumatoid arthritis [J].
Chiang, EPI ;
Bagley, PJ ;
Selhub, J ;
Nadeau, M ;
Roubenoff, R .
AMERICAN JOURNAL OF MEDICINE, 2003, 114 (04) :283-287
[25]   Vitamin B-12 deficiency induces anomalies of base substitution and methylation in the DNA of rat colonic epithelium [J].
Choi, SW ;
Friso, S ;
Ghandour, H ;
Bagley, PJ ;
Selhub, J ;
Mason, JB .
JOURNAL OF NUTRITION, 2004, 134 (04) :750-755
[26]   EFFECT OF PYRIDOXINE (VITAMIN-B6) ON DIABETIC-PATIENTS WITH PERIPHERAL NEUROPATHY [J].
COHEN, KL ;
GORECKI, GA ;
SILVERSTEIN, SB ;
EBERSOLE, JS ;
SOLOMON, LR .
JOURNAL OF THE AMERICAN PODIATRY ASSOCIATION, 1984, 74 (08) :394-397
[27]  
COLE BF, 2005, P AM ASSOC CANC RES, V46, P4399
[28]   Accumulation of mitochondrial DNA deletions is age, tissue and folate-dependent in rats [J].
Crott, JW ;
Choi, SW ;
Branda, RF ;
Mason, JB .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2005, 570 (01) :63-70
[29]   CHARACTERISTICS OF PYRIDOXINE OVERDOSE NEUROPATHY SYNDROME [J].
DALTON, K ;
DALTON, MJT .
ACTA NEUROLOGICA SCANDINAVICA, 1987, 76 (01) :8-11
[30]  
Davis SR, 2005, AM J CLIN NUTR, V81, P648