Birnbaum L S, Morrissey R E, Harris M W
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.
Toxicol Appl Pharmacol. 1991 Jan;107(1):141-52. doi: 10.1016/0041-008x(91)90338-f.
Brominated flame retardants involved in many industrial uses contain polybrominated dibenzo-p-dioxins (PBDDs) and dibenzofurans (PBDFs) as contaminants. The levels of these contaminants can be dramatically increased by combustion. These chemicals are closely related in structure to the polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs), of which 2,3,7,8-tetrachloridibenzo-p-dioxin (TCDD) is the most toxic isomer. TCDD and related PCDFs are potent mouse teratogens inducing cleft palate and hydronephrosis at doses below those at which overt maternal and embryo/fetal toxicity occurs. This study examines the teratogenic effects of 2,3,7,8-tetrabromodibenzo-p-dioxin (TBDD), 2,3,7,8-tetrabromodibenzofuran (TBDF), 1,2,3,7,8-pentabromodibenzofuran (1PeBDF), and 2,3,4,7,8-pentabromodibenzofuran (4PeBDF) in C57BL/6N mice treated on gestation day (gd) 10 and examined on gd 18. Pregnant dams were treated with 0-4000 micrograms of each congener per kilogram body weight in 10 ml corn oil/kg. Dose selection was based on the relative toxicity of the chlorinated isomers. Maternal toxicity and developmental toxicity were assessed, and the hard palate and kidney, the target organs for the teratogenic effects of TCDD and related compounds, were examined for structural abnormalities. While the maternal liver weight increased at all dose levels examined for all four compounds, there was no evidence of any maternal toxicity. Embryo/fetal mortality was increased only at greater than or equal to 500 microgram TBDF/kg, while fetal weight increased in a dose-related manner following exposure to TBDD and TBDF. All compounds produced hydronephrosis (HN) at doses below that at which cleft palate (CP) occurred. The incidence of HN was significantly increased above background levels at the following doses (micrograms/kg): TBDD, 3; TBDF, 25; 1PeBDF, 500; 4PeBDF, 400. The LOELs (micrograms/kg) for CP were: TBDD, 48; TBDF, 200; 1PeBDF, 4000; 4PeBDF, 2400. The cleft palate incidence for all four brominated compounds and TCDD could be fit to a common slope, compatible with the concept that these chemicals all exert their teratogenic effects through a common mechanism. The potency of these chemicals, relative to TCDD as 1 for the induction of cleft palate, is TBDD, 0.24; TBDF, 0.10; 1PeBDF, 0.004; and 4PeBDF, 0.005. Previous studies from our laboratory had determined that the chlorinated dibenzofuran isomers had relative potencies of 0.05 (TCDF), 0.03 (1PeCDF), and 0.09 (4PeCDF). Thus, bromination decreases the teratogenic activity of TBDD relative to TCDD and of both 1- and 4PeBDF relative to the chlorinated isomers. However, substitution of bromines for chlorines increases the potency of TBDF relative to TCDF.(ABSTRACT TRUNCATED AT 400 WORDS)
许多工业用途中涉及的溴化阻燃剂含有多溴二苯并对二噁英(PBDDs)和二苯并呋喃(PBDFs)作为污染物。这些污染物的含量在燃烧时会急剧增加。这些化学物质在结构上与多氯二苯并对二噁英(PCDDs)和二苯并呋喃(PCDFs)密切相关,其中2,3,7,8 - 四氯二苯并对二噁英(TCDD)是毒性最强的异构体。TCDD及相关的PCDFs是强效的小鼠致畸剂,在低于引起明显母体和胚胎/胎儿毒性的剂量下就能诱导腭裂和肾积水。本研究检测了2,3,7,8 - 四溴二苯并对二噁英(TBDD)、2,3,7,8 - 四溴二苯并呋喃(TBDF)、1,2,3,7,8 - 五溴二苯并呋喃(1PeBDF)和2,3,4,7,8 - 五溴二苯并呋喃(4PeBDF)对在妊娠第10天(gd)接受处理并于gd 18进行检查的C57BL/6N小鼠的致畸作用。怀孕母鼠以每千克体重0 - 4000微克的每种同系物溶于10毫升玉米油/千克的溶液进行处理。剂量选择基于氯化异构体的相对毒性。评估了母体毒性和发育毒性,并检查了硬腭和肾脏这两个TCDD及相关化合物致畸作用的靶器官是否存在结构异常。虽然在所检测的所有剂量水平下,所有四种化合物均使母体肝脏重量增加,但没有任何母体毒性的证据。仅当TBDF剂量大于或等于500微克/千克时胚胎/胎儿死亡率增加,而暴露于TBDD和TBDF后胎儿体重呈剂量相关方式增加。所有化合物在低于出现腭裂(CP)的剂量下均产生肾积水(HN)。HN的发生率在以下剂量(微克/千克)时显著高于背景水平:TBDD为3;TBDF为25;1PeBDF为500;4PeBDF为400。CP的最低观察到有害作用水平(LOELs,微克/千克)分别为:TBDD为48;TBDF为200;1PeBDF为4000;4PeBDF为2400。所有四种溴化化合物和TCDD的腭裂发生率可以拟合到一个共同斜率,这与这些化学物质均通过共同机制发挥致畸作用的概念相符。这些化学物质相对于TCDD诱导腭裂的效力(以TCDD为1)分别为:TBDD为0.24;TBDF为0.10;1PeBDF为0.004;4PeBDF为0.005。我们实验室之前的研究已确定氯化二苯并呋喃异构体的相对效力为0.05(TCDF)、0.03(1PeCDF)和0.09(4PeCDF)。因此,溴化作用相对于TCDD降低了TBDD的致畸活性,相对于氯化异构体降低了1 - 和4PeBDF的致畸活性。然而,用溴取代氯增加了TBDF相对于TCDF的效力。(摘要截短至400字)