Suppr超能文献

[通过鸡胚肝微粒体酶活性评估对油症致病物质的毒性作用]

[Evaluation of toxic effects on yusho causal substances by chick embryo hepatic microsomal enzymes activities].

作者信息

Kashimoto T, Takayama K, Mimura M, Ohta S, Miyata H

出版信息

Fukuoka Igaku Zasshi. 1989 May;80(5):210-20.

PMID:2501189
Abstract

PCBs, non-ortho chlorine substituted PCBs (Co-PCBs), PCQs and (PCDFs + PCDDs), all of which contained similar compositions of those corresponding in yusho oil, were prepared from a PCB preparation used as a heat exchanger fluid. After dissolved in 1, 4-dioxane, they were applied into the air sac of white leghorn eggs incubated for 16.5 days at 37.5 degrees C. Forty eight hours after injection, the hepatic benzo(a)pyrene hydroxylase (AHH) and 7-ethoxyresorufin deethylase (EROD) activities were assayed. The average relative potencies of induction for the two microsomal drug metabolizing enzymes by (PCDFs + PCDDs), Co-PCBs, PCBs and PCQs were 100, 13.4, 0.0006 and 0.0004, respectively. The toxic effects for yusho disease by these substances were calculated from the relative enzyme induction potencies and the average concentrations in yusho oils with the production dates of February 9 and 10, 1968. Consequently, the relative toxicities of (PCDFs+PCDDs), Co-PCBs, PCBs and PCQs were 100, 13.2, 0.06 and 0.12, respectively. This result, as well as our previous investigations using rats and monkeys, insists that (PCDFs+PCDDs) are the primary causal agents for yusho disease. However, the Co-PCBs, which were recently detected in the yusho oils by us, were revealed to be fairly effective in yusho manifestation. In addition, it was cleared that the hepatic enzyme induction by the Co-PCBs fraction, which contained other several PCB isomers, was almost completely contributed by only Co-PCBs such as 3,4,3',4'-tetra- 3,4,5,3',4'-penta- and 3,4,5,3',4',5'-hexachlorinated biphenyls present in the fraction. A chemical uptake rate from the air sac by the chick embryo decreased significantly in the cases of extremely high doses of PCBs (10,000 micrograms/egg) and PCQs (3,333 and 10,000 micrograms/egg), and result the elevations of hepatic enzymes activities were depressed, indicating that the suitable chemical dose amount to be less than about 1,000 micrograms/egg.

摘要

多氯联苯(PCBs)、非邻位氯取代多氯联苯(Co - PCBs)、多氯喹啉(PCQs)以及(多氯二苯并呋喃 + 多氯二苯并二噁英)(PCDFs + PCDDs),所有这些物质都含有与油症油中相应成分相似的组成,它们是由一种用作热交换器流体的多氯联苯制剂制备而成。溶解于1,4 - 二氧六环后,将它们注入在37.5摄氏度下孵化16.5天的白来航鸡胚的气囊中。注射48小时后,测定肝脏中苯并(a)芘羟化酶(AHH)和7 - 乙氧基异吩唑酮脱乙基酶(EROD)的活性。(PCDFs + PCDDs)、Co - PCBs、PCBs和PCQs对两种微粒体药物代谢酶的平均诱导相对效力分别为100、13.4、0.0006和0.0004。根据这些物质的相对酶诱导效力以及1968年2月9日和10日生产的油症油中的平均浓度,计算出这些物质对油症病的毒性作用。因此,(PCDFs + PCDDs)、Co - PCBs、PCBs和PCQs的相对毒性分别为100、13.2、0.06和0.12。这一结果以及我们之前使用大鼠和猴子进行的研究表明,(PCDFs + PCDDs)是油症病的主要致病因素。然而,我们最近在油症油中检测到的Co - PCBs被发现对油症的表现相当有效。此外,还明确了含有其他几种多氯联苯异构体的Co - PCBs组分对肝脏酶的诱导作用几乎完全由该组分中存在的诸如3,4,3',4'-四氯、3,4,5,3',4'-五氯和3,4,5,3',4',5'-六氯联苯等Co - PCBs贡献。在极高剂量的多氯联苯(10,000微克/蛋)和多氯喹啉(3,333和10,000微克/蛋)情况下,鸡胚从气囊的化学摄取率显著降低,并且肝脏酶活性的升高受到抑制,这表明合适的化学剂量应小于约1,000微克/蛋。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验