Direct evidence for in vivo hydroxyl radical generation in blood of mice after acute chromium(VI) intake - Electron spin resonance spin-trapping investigation

被引:19
作者
Hojo, Y [1 ]
Okado, A [1 ]
Kawazoe, S [1 ]
Mizutani, T [1 ]
机构
[1] Kyoto Prefectural Univ, Dept Food Sci & Nutr Hlth, Kyoto 6068522, Japan
关键词
chromium(VI); hydroxyl radical; blood; in vivo; mice; ESR; spin-trapping; DMPO;
D O I
10.1385/BTER:76:1:75
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
Although it is assumed from in vitro experiments that the hydroxyl radical ( OH) may be responsible for chromium(VI) toxicity/ carcinogenicity, no electron spin resonance (ESR) evidence for the gen eration of . OH in vivo has been reported. In this study, we have employed an ESR spin-trapping technique with 5,5-dimethylpyrrolineN-oxide (DMPO), a selective OH trap, to detect . OH in blood. The ESR spectrum of spin adduct observed in the blood of mice given 4.8 mmol Cr(VI)/kg body weight exhibited the 1 : 2: 2: 1 intensity pattern of a quartet with a hyperfine coupling constant A(N) = A(H) = 14.81 G and g-value = 2.0067. The concentration of the spin adduct detected in the blood was 7.37 mu M The adduct production was inhibited by the addition of specific OH scavengers such as sodium benzoate and methional to the blood. The results indicate that the spin adduct is nitroxide produced by the reaction of OH with DMPO. This is the first report of ESR evidence for the in vivo generation of OH in mammals by Cr(VI).
引用
收藏
页码:75 / 84
页数:10
相关论文
共 28 条
[21]   CHROMIUM(V) AND HYDROXYL RADICAL FORMATION DURING THE GLUTATHIONE REDUCTASE-CATALYZED REDUCTION OF CHROMIUM(VI) [J].
SHI, XL ;
DALAL, NS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (01) :627-634
[22]   ON THE HYDROXYL RADICAL FORMATION IN THE REACTION BETWEEN HYDROGEN-PEROXIDE AND BIOLOGICALLY GENERATED CHROMIUM(V) SPECIES [J].
SHI, XL ;
DALAL, NS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 277 (02) :342-350
[23]   IS THERE A ROLE FOR REACTIVE OXYGEN SPECIES IN THE MECHANISM OF CHROMIUM(VI) CARCINOGENESIS [J].
STANDEVEN, AM ;
WETTERHAHN, KE .
CHEMICAL RESEARCH IN TOXICOLOGY, 1991, 4 (06) :616-625
[24]   SYNTHESES, STRUCTURES, AND REACTIVITIES OF SYNTHETIC ANALOGS OF THE 3 FORMS OF CO(III)-BLEOMYCIN - PROPOSED MODE OF LIGHT-INDUCED DNA DAMAGE BY THE CO(III) CHELATE OF THE DRUG [J].
TAN, JD ;
HUDSON, SE ;
BROWN, SJ ;
OLMSTEAD, MM ;
MASCHARAK, PK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (10) :3841-3853
[25]  
THORNALLEY PJ, 1986, LIFE CHEM REPORTS, V4, P57
[26]  
VEILLON C, 1986, IARC SCI PUBL, V71, P433
[27]  
YAMAMOTO K, 1989, J BIOL CHEM, V264, P15435
[28]   SITE-SPECIFIC DNA DAMAGE INDUCED BY COBALT(II) ION AND HYDROGEN-PEROXIDE - ROLE OF SINGLET OXYGEN [J].
YAMAMOTO, K ;
INOUE, S ;
YAMAZAKI, A ;
YOSHINAGA, T ;
KAWANISHI, S .
CHEMICAL RESEARCH IN TOXICOLOGY, 1989, 2 (04) :234-239