Literature DB >> 6832100

Determination of 2-acetylaminofluorene adducts by immunoassay.

M C Poirier, B True, B A Laishes.   

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.

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Year:  1983        PMID: 6832100      PMCID: PMC1569126          DOI: 10.1289/ehp.834993

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  15 in total

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4.  Persistent binding of a new reaction product of the carcinogen N-hydroxy-N-2-acetylaminofluorene with guanine in rat liver DNA in vivo.

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Journal:  Cancer Res       Date:  1972-10       Impact factor: 12.701

5.  Influence of liver regeneration on the loss of fluorenylacetamide derivative bound to liver DNA.

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6.  Stability of binding of label from N-hydroxy-N-2-fluorenylacetamide to intracellular targets, particularly deoxyribonucleic acid in rat liver.

Authors:  D Szafarz; J H Weisburger
Journal:  Cancer Res       Date:  1969-04       Impact factor: 12.701

7.  Persistent binding of 2-acetylaminofluorene to rat liver DNA in vivo and consideration of the mechanism of binding of N-hydroxy-2-acetylaminofluorene to rat liver nucleic acids.

Authors:  C C Irving; R A Veazey
Journal:  Cancer Res       Date:  1969-10       Impact factor: 12.701

Review 8.  Metabolic activation of N-hydroxy compounds by conjugation.

Authors:  C C Irving
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Authors:  F A Beland; K L Dooley; D A Casciano
Journal:  J Chromatogr       Date:  1979-06-01

10.  Formation and removal of specific acetylaminofluorene-DNA adducts in mouse and human cells measured by radioimmunoassay.

Authors:  M C Poirier; M A Dubin; S H Yuspa
Journal:  Cancer Res       Date:  1979-04       Impact factor: 12.701

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3.  Formation and persistence of arylamine DNA adducts in vivo.

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Journal:  Environ Health Perspect       Date:  1985-10       Impact factor: 9.031

Review 4.  Gene activation studied by immunological methods.

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5.  Use of 2-acetamidophenanthrene and 2-acetamidofluorene in investigations of mechanisms of hepatocarcinogenesis.

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