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黄曲霉毒素B1诱导Fischer 344大鼠脾淋巴细胞的次黄嘌呤磷酸核糖转移酶(Hprt)突变。一项间歇性喂养试验的结果

Aflatoxin B1-induced Hprt mutations in splenic lymphocytes of Fischer 344 rats. Results of an intermittent feeding trial.

作者信息

Morris S M, Aidoo A, Chen J J, Chou M W, Casciano D A

机构信息

Division of Genetic and Reproductive Toxicology, National Center for Toxicological Research, Food and Drug Administration, Department of Health and Human Services, 3900 NCTR Road, Jefferson, AR 72079, USA.

出版信息

Mutat Res. 1999 Jan 25;423(1-2):33-8. doi: 10.1016/s0027-5107(98)00222-x.

Abstract

In a previous study, we found an increase in the mutant frequency at the Hypoxanthine phosphoribosyl transferase (Hprt) locus in the splenic lymphocytes of Fischer 344 rats acutely exposed to aflatoxin B1 (AFB1). Because an acute exposure may not reflect the exposure pattern of individuals whose diet may contain AFB1-contaminated foodstuffs, we sought to determine if the feeding regimen affected the induction of Hprt mutations in the rat splenic lymphocyte. Thus, Fischer 344 rats were fed either (A) a control diet, (B) various doses of AFB1 for three four-week periods interspersed with two four-week periods of the control diet, or (C) continuously fed 1.6 ppm of AFB1. Not only was a significant increase in the mutant frequency detected in the lymphocytes of rats fed a dose as low as 0. 01 ppm of AFB1, but the increase in the mutant frequency at the end of the 20-week experimental period was consistent with an accumulation of damage induced by AFB1. These results indicate that the rat lymphocyte/Hprt assay is useful for detecting chronic low level exposures. Further, these data suggest that an intermittent, low-level exposure to AFB1 may present a human health risk.

摘要

在之前的一项研究中,我们发现急性暴露于黄曲霉毒素B1(AFB1)的Fischer 344大鼠脾淋巴细胞中,次黄嘌呤磷酸核糖基转移酶(Hprt)位点的突变频率增加。由于急性暴露可能无法反映饮食中可能含有受AFB1污染食物的个体的暴露模式,我们试图确定喂养方案是否会影响大鼠脾淋巴细胞中Hprt突变的诱导。因此,Fischer 344大鼠被喂食以下几种食物:(A)对照饮食;(B)在三个为期四周的时间段内喂食不同剂量的AFB1,期间穿插两个为期四周的对照饮食时间段;或(C)持续喂食1.6 ppm的AFB1。不仅在喂食低至0.01 ppm AFB1剂量的大鼠淋巴细胞中检测到突变频率显著增加,而且在20周实验期结束时突变频率的增加与AFB1诱导的损伤积累一致。这些结果表明,大鼠淋巴细胞/Hprt检测法可用于检测慢性低水平暴露。此外,这些数据表明,间歇性低水平暴露于AFB1可能对人类健康构成风险。

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