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家用燃油炉排放物的化学和毒理学特性:II. 致突变性、致癌性和潜在致畸活性。

Chemical and toxicological characterization of residential oil burner emissions: II. Mutagenic, tumorigenic, and potential teratogenic activity.

作者信息

Braun A G, Busby W F, Liber H L, Thilly W G

机构信息

Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Environ Health Perspect. 1987 Aug;73:235-46. doi: 10.1289/ehp.8773235.

Abstract

Extracts of effluents from a modern residential oil burner have been evaluated in several toxicological assay systems. Bacterial mutagens were detected in extracts from both the particulate and vapor phase emissions. Effluents from continuous operation were an order of magnitude less mutagenic than those from cyclic (5 min on, 10 min off) operations. No difference in the yield of bacterial mutagens per gram of fuel burned was found between cyclic operation under low and moderate sooting conditions. On the basis of elution behavior from alumina it appeared that the bacterial mutagens collected from high sooting effluents were more polar than those from low sooting effluent. An extract that was mutagenic in bacteria did not induce a significant increase in mutation frequency to human lymphoblasts. No evidence of tumorigenicity was observed in a limited number of newborn mice after IP injection of effluent extract when compared to historical control data. Putative nonmutagenic teratogens were detected in effluent using an attachment inhibition assay. The level of these agents was reduced in effluents from continuous oil burner operation.

摘要

在多个毒理学检测系统中对现代家用燃油燃烧器排放物的提取物进行了评估。在颗粒物和气相排放物的提取物中均检测到了细菌诱变剂。连续运行的排放物的诱变性比循环运行(开5分钟,关10分钟)的排放物低一个数量级。在低积炭和中等积炭条件下的循环运行中,每克燃烧燃料产生的细菌诱变剂产量没有差异。根据从氧化铝上的洗脱行为,似乎从高积炭排放物中收集到的细菌诱变剂比低积炭排放物中的更具极性。在细菌中具有诱变性的一种提取物并未导致人类淋巴母细胞的突变频率显著增加。与历史对照数据相比,在有限数量的新生小鼠腹腔注射排放物提取物后未观察到致瘤性证据。使用附着抑制试验在排放物中检测到了推定的非诱变致畸剂。在燃油燃烧器连续运行产生的排放物中,这些物质的含量有所降低。

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Bioassay of extracts of ambient particulate matter.环境颗粒物提取物的生物测定。
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本文引用的文献

1
Quantitative assay for mutation in diploid human lymphoblasts using microtiter plates.
Anal Biochem. 1981 Jan 1;110(1):1-8. doi: 10.1016/0003-2697(81)90103-2.

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