Enzymatic methylation of arsenic compounds.: VII.: Monomethylarsonous acid (MMAIII) is the substrate for MMA methyltransferase of rabbit liver and human hepatocytes

被引:97
作者
Zakharyan, RA
Ayala-Fierro, F
Cullen, WR
Carter, DM
Aposhian, HV
机构
[1] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA
[3] Univ Arizona, Ctr Toxicol, Tucson, AZ 85721 USA
[4] Univ British Columbia, Dept Chem, Vancouver, BC, Canada
关键词
D O I
10.1006/taap.1999.8687
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inorganic arsenite is methylated by some, but not all, animal species to dimethylarsinic acid (DMA), The monomethyl compound containing arsenic in an oxidation state of +3 has been proposed as an intermediate. Using highly purified arsenic methyltransferase from rabbit liver and the partially purified enzyme from Chang human liver hepatocytes, the activity of methylarsonic acid (MMA(V)) and methylarsonous acid (MMA(III)) as a substrate has been characterized by Michaelis-Menten kinetics. The rabbit liver enzyme has a greater affinity for MMA(III) (K-m = 0.92 x 10(-5) M) than MMA(V) (K-m = 7.0 x 10(-5) M) since the smaller the K, the greater the affinity. In addition, a dithiol, reduced lipoic acid or dithiothreitol, appears to be more active than GSH in satisfying the thiol requirement of the enzyme. Although investigators have been unable to detect the arsenic methyltransferase in surgically removed human liver, its presence in Chang human hepatocytes now has been established. The K-m for MMA(III), 3.04 x 10(-6), using MMAIII methyltransferase from Chang human hepatocytes was not greatly different from that of the rabbit liver enzyme, (C) 1999 Academic Press.
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页码:9 / 15
页数:7
相关论文
共 33 条
[1]   Enzymatic methylation of arsenic species and other new approaches to arsenic toxicity [J].
Aposhian, HV .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1997, 37 :397-419
[2]   NEWER DEVELOPMENTS IN ARSENIC TOXICITY [J].
APOSHIAN, HV ;
APOSHIAN, MM .
JOURNAL OF THE AMERICAN COLLEGE OF TOXICOLOGY, 1989, 8 (07) :1297-1305
[3]  
APOSHIAN HV, 1997, J PHARMACOL EXP THER, V277, P938
[4]   ARSENIC BINDING-PROTEINS OF MAMMALIAN SYSTEMS .1. ISOLATION OF 3 ARSENITE-BINDING PROTEINS OF RABBIT LIVER [J].
BOGDAN, GM ;
SAMPAYOREYES, A ;
APOSHIAN, HV .
TOXICOLOGY, 1994, 93 (2-3) :175-193
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   STUDY OF INORGANIC ARSENIC METHYLATION BY RAT-LIVER INVITRO - RELEVANCE FOR THE INTERPRETATION OF OBSERVATIONS IN MAN [J].
BUCHET, JP ;
LAUWERYS, R .
ARCHIVES OF TOXICOLOGY, 1985, 57 (02) :125-129
[7]   ROLE OF THIOLS IN THE INVITRO METHYLATION OF INORGANIC ARSENIC BY RAT-LIVER CYTOSOL [J].
BUCHET, JP ;
LAUWERYS, R .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (16) :3149-3153
[8]   A new type of compound containing arsenic [J].
Burrows, GJ ;
Turner, EE .
JOURNAL OF THE CHEMICAL SOCIETY, 1920, 117 :1373-1383
[9]   CHRONIC ARSENIC POISONING IN THE NORTH OF MEXICO [J].
CEBRIAN, ME ;
ALBORES, A ;
AGUILAR, M ;
BLAKELY, E .
HUMAN TOXICOLOGY, 1983, 2 (01) :121-133
[10]   BIOLOGICAL METHYLATION [J].
CHALLENGER, F .
CHEMICAL REVIEWS, 1945, 36 (03) :315-361