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静脉注射混合物后,大鼠肝脏对有毒多氯二苯并对二噁英和二苯并呋喃的选择性保留。

Selective retention of toxic polychlorinated dibenzo-p-dioxins and dibenzofurans in the liver of the rat after intravenous administration of a mixture.

作者信息

van den Berg M, van Wijnen J, Wever H, Seinen W

机构信息

Laboratory of Environmental and Toxicological Chemistry, University of Amsterdam, The Netherlands.

出版信息

Toxicology. 1989 Apr;55(1-2):173-82. doi: 10.1016/0300-483x(89)90184-4.

Abstract

A mixture of polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs), purified from fly ash from a municipal incinerator, was administered as a single intravenous dose to male rats. Livers were analyzed after 5 h, 1, 2, 4, 7 and 9 days for PCDD and PCDF content. Starting from t = 5 h 2,3,7,8-substituted congeners were the predominant PCDDs and PCDFs retained. 2,3,4,6,7-PnCDF was the only congener without 4 lateral chlorine atoms retained in the liver. For most of the 2,3,7,8-substituted congeners reliable half-lives could not be calculated due to the short experimental period. For only three 2,3,7,8-substituted congeners was a complete elimination from the liver found, within this time period. These congeners were 2,3,7,8-TCDF, 1,2,3,7,8- and 2,3,4,6,7-PnCDF with half-lives of less than 1, 2.1 and 1.6 days, respectively. The other PCDDs and PCDFs, without 4 lateral chlorine atoms, were not detected in the liver from 5 h to 9 days after i.v. administration. Based on the congeneric distribution patterns, it is suggested that besides metabolism, structural specific binding to the Ah-receptor and cytochrome P-450 complex might also be responsible for this selective liver retention.

摘要

从城市垃圾焚烧炉飞灰中提纯的多氯二苯并对二噁英(PCDDs)和二苯并呋喃(PCDFs)混合物,以单次静脉注射剂量给予雄性大鼠。在注射后5小时、1天、2天、4天、7天和9天对肝脏进行分析,检测PCDD和PCDF含量。从t = 5小时开始,2,3,7,8 - 取代同系物是肝脏中保留的主要PCDDs和PCDFs。2,3,4,6,7 - 五氯二苯并呋喃是肝脏中唯一保留的没有4个侧位氯原子的同系物。由于实验周期短,对于大多数2,3,7,8 - 取代同系物,无法计算出可靠的半衰期。在此时间段内,仅发现三种2,3,7,8 - 取代同系物能从肝脏中完全消除。这些同系物是2,3,7,8 - 四氯二苯并呋喃、1,2,3,7,8 - 和2,3,4,6,7 - 五氯二苯并呋喃,半衰期分别小于1天、2.1天和1.6天。静脉注射后5小时至9天,肝脏中未检测到其他没有4个侧位氯原子的PCDDs和PCDFs。根据同系物分布模式,表明除代谢外,与芳烃受体和细胞色素P - 450复合物的结构特异性结合也可能是肝脏选择性保留的原因。

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