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意大利中部赤狐和人体脂肪组织中多氯联苯及2,3,7,8-四氯二苯并对二噁英当量(TEQs)的异构体特异性分析。

Isomer-specific analysis of polychlorinated biphenyls and 2,3,7,8-tetrachlorodibenzo-p-dioxin equivalents (TEQs) in red fox and human adipose tissue from central Italy.

作者信息

Corsolini S, Focardi S, Kannan K, Tanabe S, Tatsukawa R

机构信息

Dipartimento di Biologia Ambientale, Università di Siena, Italy.

出版信息

Arch Environ Contam Toxicol. 1995 Jul;29(1):61-8. doi: 10.1007/BF00213088.

Abstract

The general exposure of humans and foxes to polychlorinated biphenyls (PCBs) and DDT in Italy was determined by analysis of adipose tissue samples collected from 1991-1992. sigma PCB concentrations varied between 1.0 and 2.6 micrograms/g (wet wt.). sigma DDT concentrations ranged from 1.6 to 5.0 micrograms/g (wet wt.). About thirty-five PCB congeners were identified in most samples. PCB congeners of IUPAC Nos. 138, 153, and 180 were the most abundant compounds, accounting for an average of 50% of the sigma PCBs in humans and 64% in foxes. Generally, higher chlorinated biphenyls and those with a 2,4,5-chlorine substitution in one ring and at least one substitution in the 4-position of the other ring were preferentially accumulated. Coplanar PCB congeners were detected at considerable concentrations and there is no sign of decline in their concentrations with respect to previously reported data. IUPAC Nos. 118, 156 and 126 were the main contributors to toxicity in humans and foxes. The significant contribution of mono-ortho congeners in humans and non-ortho congeners in foxes suggests that differences in metabolic potential may affect the PCB toxicity pattern.

摘要

通过对1991年至1992年采集的脂肪组织样本进行分析,确定了意大利人类和狐狸对多氯联苯(PCBs)和滴滴涕(DDT)的总体暴露情况。总多氯联苯浓度在1.0至2.6微克/克(湿重)之间变化。总滴滴涕浓度范围为1.6至5.0微克/克(湿重)。在大多数样本中鉴定出约35种多氯联苯同系物。国际纯粹与应用化学联合会(IUPAC)编号为138、153和180的多氯联苯同系物是含量最高的化合物,在人类体内平均占总多氯联苯的50%,在狐狸体内占64%。一般来说,氯含量较高的多氯联苯以及在一个环上有2,4,5-氯取代且在另一个环的4位至少有一个取代的多氯联苯更容易蓄积。共平面多氯联苯同系物的检测浓度相当,且与先前报告的数据相比,其浓度没有下降的迹象。IUPAC编号为118、156和126的同系物是人类和狐狸中毒性的主要贡献者。单邻位同系物在人类中的显著贡献以及非邻位同系物在狐狸中的显著贡献表明,代谢潜力的差异可能会影响多氯联苯的毒性模式。

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