Kinetic parameters and intraindividual fluctuations of ochratoxin A plasma levels in humans

被引:211
作者
Studer-Rohr, I
Schlatter, J
Dietrich, DR
机构
[1] Univ Constance, Dept Environm Toxicol, D-78457 Constance, Germany
[2] Swiss Fed Inst Technol, Inst Toxicol, CH-8603 Schwerzenbach, Switzerland
[3] Univ Zurich, CH-8603 Schwerzenbach, Switzerland
[4] Swiss Fed Off Publ Hlth, Div Food Sci, Toxicol Sect, Zurich, Switzerland
[5] Swiss Fed Inst Technol, Dept Food Sci, CH-8092 Zurich, Switzerland
关键词
ochratoxin A; kinetics; humans; plasma levels; cancer risk extrapolation;
D O I
10.1007/s002040000157
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The mycotoxin ochratoxin A (OTA) is a rodent carcinogen produced by species of the ubiquitous fungal genera Aspergillus and Penicillium. OTA is found in a variety of food items and as a consequence is also found in human plasma (average concentrations found in this study: 0.1-1 ng OTA/ml plasma). To improve the scientific basis for cancer risk assessment the toxicokinetic profile of OTA was studied in one human volunteer following ingestion of 395 ng H-3-labeled OTA (3.8 mu Ci). A two-compartment open model consisting of a central compartment was found to best describe the in vivo data. This two-compartment model consisted of a fast elimination and distribution phase (T-1/2 about 20 h) followed by a slow elimination phase (renal clearance about 0.11 ml/min.) and a calculated plasma half-life of 35.55 days. This half-life was approximately eight times longer than that determined previously in rats, In addition, the intraindividual fluctuation of OTA plasma levels was investigated in eight individuals over a period of 2 months, The concentrations determined ranged between 0.2 and 0.9 ng OTA/ml plasma. The plasma levels in some individuals remained nearly constant over time, while others varied considerably (e.g. increase of 0.4 ng/ml within 3 days, decrease of 0.3 ng/ml within 5 days) during the observation period. This intraindividual fluctuation in OTA plasma levels, which may represent differences in OTA exposure and/or metabolism, as well as the large difference in plasma half-life in humans compared to rats must be taken into consideration when the results of rat cancer study data are extrapolated to humans for risk assessment purposes.
引用
收藏
页码:499 / 510
页数:12
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