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经气管内给药的黄曲霉毒素B1的药代动力学

Pharmacokinetics of intratracheally administered aflatoxin B1.

作者信息

Coulombe R A, Huie J M, Ball R W, Sharma R P, Wilson D W

机构信息

Department of Veterinary Science, Utah State University, Logan 84322-4620.

出版信息

Toxicol Appl Pharmacol. 1991 Jun 15;109(2):196-206. doi: 10.1016/0041-008x(91)90168-e.

Abstract

High concentrations of the carcinogen aflatoxin B1 (AFB1) are commonly found in respirable, airborne grain dusts, and inhaled AFB1 has been shown to be a risk factor for occupational pulmonary carcinogenesis. The fate of AFB1 exposure via the respiratory tract is therefore of interest in an evaluation of potential occupational risk. The pharmacokinetic disposition of intratracheally administered AFB1 was studied in male Sprague-Dawley rats. Blood and tissues were sampled at selected intervals for 3 weeks following administration of a single dose of grain dust-adsorbed or microcrystalline [3H]AFB1 (6 micro-Ci: microgramsg/kg). The blood concentration-time profiles from both groups best approximated a two-compartment open model with first-order absorption. The first-order absorption rate constant was significantly less in the animals given dust-adsorbed AFB1 than in those receiving microcrystalline AFB1 (0.083 vs -0.1060 min -1, respectively), although the first-order elimination rate constants for both groups were nearly identical (0.00928 and 0.00921 hr-1, respectively). Blood concentrations of the AFB1 metabolites AFM1, AFQ1, AFL, and AFP1 showed little differences among the two groups. The tissue concentrations of aflatoxins for the microcrystalline group were significantly greater at 3 hr in all tissues examined except for the trachea and lung in which those for the dust-adsorbed group were greater. At 3 days and 3 weeks, no significant differences between exposure groups were seen in any tissue except fat, where the amount of aflatoxins was greater for the dust-adsorbed group. AFB1 binding to DNA was significantly greater in the trachea and lung of the dust-adsorbed group compared to that in the microcrystalline group at 3 hr, whereas in the liver the AFB1-DNA binding in the microcrystalline group was significantly greater during this time. Thus, particle association of AFB1 increased the respiratory tract retention of this compound at early time intervals, which might be a factor in the reputed carcinogenic action of this compound in the respiratory tract. These findings may be useful as part of a comprehensive study to evaluate the disposition of AFB1 in individuals exposed to grain dusts laden with this carcinogen.

摘要

在可吸入的空气中谷物粉尘中通常会发现高浓度的致癌物黄曲霉毒素B1(AFB1),并且已表明吸入AFB1是职业性肺致癌的一个风险因素。因此,在评估潜在职业风险时,通过呼吸道接触AFB1的转归受到关注。在雄性Sprague-Dawley大鼠中研究了气管内给予AFB1后的药代动力学情况。在单次给予谷物粉尘吸附的或微晶[3H]AFB1(6微居里/微克/千克)后,每隔一定时间采集血液和组织样本,持续3周。两组的血药浓度-时间曲线最符合具有一级吸收的二室开放模型。给予粉尘吸附的AFB1的动物的一级吸收速率常数显著低于接受微晶AFB1的动物(分别为0.083和-0.1060分钟-1),尽管两组的一级消除速率常数几乎相同(分别为0.00928和0.00921小时-1)。AFB1代谢产物AFM1、AFQ1、AFL和AFP1的血药浓度在两组之间几乎没有差异。微晶组的黄曲霉毒素组织浓度在3小时时,除气管和肺外,在所检查的所有组织中均显著更高,而在气管和肺中,粉尘吸附组的黄曲霉毒素组织浓度更高。在3天和3周时,除脂肪外,各暴露组在任何组织中均未观察到显著差异,在脂肪中,粉尘吸附组的黄曲霉毒素含量更高。在3小时时,与微晶组相比,粉尘吸附组气管和肺中AFB1与DNA的结合显著更高,而在此期间,微晶组肝脏中的AFB1-DNA结合显著更高。因此,AFB1与颗粒的结合在早期时间段增加了该化合物在呼吸道的滞留,这可能是该化合物在呼吸道中具有公认致癌作用的一个因素。这些发现可能有助于作为一项综合研究的一部分,以评估AFB1在接触含有这种致癌物的谷物粉尘的个体中的转归情况。

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