SPECIATION OF MERCURY IN THE PRIMATE BLOOD AND BRAIN FOLLOWING LONG-TERM EXPOSURE TO METHYL MERCURY

被引:107
作者
VAHTER, M [1 ]
MOTTET, NK [1 ]
FRIBERG, L [1 ]
LIND, B [1 ]
SHEN, DD [1 ]
BURBACHER, T [1 ]
机构
[1] UNIV WASHINGTON,DEPT PATHOL ENVIRONM HLTH & PHARMACEUT,SEATTLE,WA 98195
关键词
D O I
10.1006/taap.1994.1026
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Total (I-Hg) and inorganic (I-Hg) mercury in blood and brain of female Macaca fascicularis monkeys, exposed to daily peroral doses of methyl mercury (MeHg; 50 μg Hg/kg body wt) for 6, 12, or 18 months, or to continuous iv infusion of HgCI2 (200 μg Hg/kg body wt) for 3 months, were determined. In normal weight monkeys (2.4-4.1 kg body wt) exposed to MeHg, steady state of T-Hg in blood (1.1 μg Hg/g) was reached in about 4 months. The elimination T 1 2 in blood was 26 days. I-Hg constituted 7% of T-Hg in blood. The average concentration of MeHg in occipital pole and thalamus was about 3 μg Hg/g at 6 months and 4.5 μg Hg/g at 12-18 months. Accumulation in brain seemed to be biphasic. Following termination of 12 months exposure, elimination T 1 2 for MeHg in brain was 35 days. I-Hg constituted about 9% of T-Hg in brain at 6-12 months, 18% at 18 months, and 74% at 6 months after termination of exposure. The I-Hg concentrations were somewhat higher in thalamus than in occipital pole. The elimination T 1 2 for I-Hg was extremely long, on the order of years. Most likely, the I-Hg was formed by demethylation of MeHg in the brain. In monkeys exposed to HgCl2, blood levels of 0.6 μg I-Hg/g gave rise to brain I-Hg levels of about 0.1 μg/g only. In three heavy weight monkeys (5.0-6.1 kg body wt) exposed to MeHg, blood Hg increased to about 2 μg Hg/g, indicating a limited distribution of MeHg to fat. The Hg concentrations in brain (7-22 μg Hg/g) were considerably higher than those in normal weight monkeys, due to the high blood Hg levels in combination with a high brain-to-blood distribution ratio. © 1994 Academic Press, Inc.
引用
收藏
页码:221 / 229
页数:9
相关论文
共 43 条
[1]   VARIATION OF BIOLOGICAL HALF-LIFE OF METHYLMERCURY IN MAN [J].
ALSHAHRISTANI, H ;
SHIHAB, KM .
ARCHIVES OF ENVIRONMENTAL HEALTH, 1974, 28 (06) :342-344
[2]   MERCURY NEUROTOXICITY - MECHANISMS OF BLOOD-BRAIN-BARRIER TRANSPORT [J].
ASCHNER, M ;
ASCHNER, JL .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1990, 14 (02) :169-176
[3]   UPTAKE OF METHYLMERCURY IN THE RAT-BRAIN - EFFECTS OF AMINO-ACIDS [J].
ASCHNER, M ;
CLARKSON, TW .
BRAIN RESEARCH, 1988, 462 (01) :31-39
[4]   METHYLMERCURY POISONING IN IRAQ - INTERUNIVERSITY REPORT [J].
BAKIR, F ;
DAMLUJI, SF ;
AMINZAKI, L ;
MURTADHA, M ;
KHALIDI, A ;
ALRAWI, NY ;
TIKRITI, S ;
DHAHIR, HI ;
CLARKSON, TW ;
SMITH, JC ;
DOHERTY, RA .
SCIENCE, 1973, 181 (4096) :230-241
[5]   DOSE-DEPENDENCE OF METHYLMERCURY METABOLISM [J].
BERLIN, M ;
CARLSON, J ;
NORSETH, T .
ARCHIVES OF ENVIRONMENTAL HEALTH, 1975, 30 (06) :307-313
[6]  
Berlin M, 1986, HDB TOXICOLOGY METAL, P387
[7]   BIOCHEMICAL AND MORPHOLOGICAL-STUDIES OF MONKEYS CHRONICALLY EXPOSED TO METHYLMERCURY [J].
CHEN, WJ ;
BODY, RL ;
MOTTET, NK .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1983, 12 (2-3) :407-416
[8]  
DOCK L, 1994, IN PRESS PHARM TOXIC
[9]   METHYLMERCURY - EXPOSURE DURATION AND REGIONAL DISTRIBUTION AS DETERMINANTS OF NEUROTOXICITY IN NONHUMAN-PRIMATES [J].
EVANS, HL ;
GARMAN, RH ;
WEISS, B .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1977, 41 (01) :15-33
[10]   PHYSIOLOGICAL MODEL FOR THE PHARMACOKINETICS OF METHYL MERCURY IN THE GROWING RAT [J].
FARRIS, FF ;
DEDRICK, RL ;
ALLEN, PV ;
SMITH, JC .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1993, 119 (01) :74-90