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免疫分析法测定2-乙酰氨基芴加合物

Determination of 2-acetylaminofluorene adducts by immunoassay.

作者信息

Poirier M C, True B, Laishes B A

出版信息

Environ Health Perspect. 1983 Mar;49:93-9. doi: 10.1289/ehp.834993.

Abstract

Antisera elicited in rabbits were used in radioimmunoassay (RIA) and enzyme-linked immunosorbent assay (ELISA) to determine femtomole quantities of deoxyguanosin-(8-yl)-acetylaminofluorene (dg-8-AAF) and deoxyguanosin-(8-yl)-aminofluorene (dg-8-AF). These adducts have been monitored in liver and kidney DNA of male Wistar-Furth rats fed 0.02% or 0.04% 2-acetylaminofluorene (2-AAF) either continuously or for a limited time followed by an interval on control diet. After 24 hr of 0.02% 2-AAF feeding, substantial levels of binding (80 fmole/mug DNA) were observed in liver DNA and increased with time, reaching a plateau of approximately 230 fmole/mug DNA at 30 days and thereafter. During the first week of continuous feeding about 80% of the total C-8 adducts in the liver DNA were deacetylated (dG-8-AF). By 25-60 days, dG-8-AF represented 97-100% of all C-8 adducts as measured by RIA and confirmed by HPLC. Values for C-8 adduct formation in kidney DNA were severalfold lower than in liver and dG-8-AF represented >90% of C-8 adducts at all times studied. In removal or repair experiments, rats were fed 2-AAF for 3, 7 or 28 days, the 2-AAF diet was discontinued and the liver adducts assayed after intervals on control diet. When dietary 2-AAF administration was for 3 or 7 days, removal of adducts was efficient and almost complete by 28 days on control diet, with preferential retention of dG-8-AF. However, when dietary 2-AAF administration was for 28 days, adduct levels were higher, the repair capacity was saturated and the removal of C-8 adducts was not complete after control diet for a 28-day interval. In a preliminary experiment when [(3)H]-2-AAF was fed for 3 days, after 25 days of 0.02% 2-AAF, the rates of newly formed adduct formation and removal were similar to those observed for the initial 3 days of 2-AAF feeding. These results demonstrate the predominance and persistence of dG-8-AF in liver and kidney DNA of 2-AAF-fed rats and suggest that the repair capacity of the whole rat liver was not diminished after 1 month of 2-AAF feeding.

摘要

在放射免疫分析(RIA)和酶联免疫吸附测定(ELISA)中使用兔体内产生的抗血清来测定飞摩尔量的脱氧鸟苷 -(8 - 基)- 乙酰氨基芴(dg - 8 - AAF)和脱氧鸟苷 -(8 - 基)- 氨基芴(dg - 8 - AF)。对雄性Wistar - Furth大鼠连续或限时饲喂0.02%或0.04%的2 - 乙酰氨基芴(2 - AAF),随后间隔一段时间喂饲对照饲料,监测其肝脏和肾脏DNA中的这些加合物。在饲喂0.02% 2 - AAF 24小时后,在肝脏DNA中观察到大量的结合水平(80飞摩尔/微克DNA),并随时间增加,在30天时达到约230飞摩尔/微克DNA的平台期,此后保持稳定。在连续饲喂的第一周,肝脏DNA中约80%的总C - 8加合物被脱乙酰化(dG - 8 - AF)。到25 - 60天时,通过RIA测定并经高效液相色谱法(HPLC)确认,dG - 8 - AF占所有C - 8加合物的97 - 100%。肾脏DNA中C - 8加合物形成的值比肝脏中的低几倍,并且在所有研究时间点dG - 8 - AF占C - 8加合物的比例均大于90%。在去除或修复实验中,大鼠饲喂2 - AAF 3、7或28天,停止饲喂2 - AAF饲料,在喂饲对照饲料一段时间后测定肝脏加合物。当给予2 - AAF饲料3天或7天时,加合物的去除效率很高,在对照饲料喂养28天时几乎完全去除,dG - 8 - AF优先保留。然而,当给予2 - AAF饲料28天时,加合物水平较高,修复能力饱和,在对照饲料喂养28天的间隔后,C - 8加合物的去除并不完全。在一个初步实验中,当饲喂[(3)H] - 2 - AAF 3天时,在0.02% 2 - AAF饲喂25天后,新形成加合物的形成和去除速率与2 - AAF饲喂最初3天观察到的速率相似。这些结果表明,在饲喂2 - AAF的大鼠肝脏和肾脏DNA中,dG - 8 - AF占主导且持续存在,并且表明在2 - AAF饲喂1个月后,整个大鼠肝脏的修复能力并未降低。

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