Strain Differences in Susceptibility to 2‐Acetylaminofluorene and Phenobarbital Promotion of Rat Hepatocarcinogenesis in a Medium‐term Assay System: Quantitation of Glutathione S‐Transferase P‐positive Foci Development
Strain Differences in Susceptibility to 2‐Acetylaminofluorene and Phenobarbital Promotion of Rat Hepatocarcinogenesis in a Medium‐term Assay System: Quantitation of Glutathione S‐Transferase P‐positive Foci Development
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中期检测系统中对 2-乙酰氨基芴和苯巴比妥促进大鼠肝癌发生的敏感性的菌株差异:谷胱甘肽 S-转移酶 P 阳性病灶发育的定量
DOI:
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发表时间:
1989
期刊:
影响因子:
--
通讯作者:
S. Nagase
中科院分区:
文献类型:
--
作者:
M. Asamoto;H. Tsuda;M. Kagawa;J. D. de Camargo;N. Ito;S. Nagase
Strain differences in susceptibility to promotion by the liver carcinogens 2‐acetylaminofluorene (2‐AAF) and phenobarbital (PB) were examined in the medium‐term bioassay system initially developed in our laboratory using male F344 rats as the test animal and glutathione S‐transferase placental form (GST‐P)‐positive foci as the lesion end‐point. Numbers and areas per cm2 of induced GST‐P‐positive hepatocellular foci were compared in LEW, F344, NAR, SD, WBN, SHR, Wistar and ODS rats initiated with diethylnitrosamine (DEN) and subjected to partial hepatectomy during subsequent administration of 2‐AAF or PB. LEW, SD, WBN, and F344 rats were most susceptible to hepatopromotion by both compounds, with a hundred fold increase in lesion area being observed for 2‐AAF in the LEW case. NAR and SHR strains demonstrated an intermediate response, while Wistar and, in particular, the related ODS rats demonstrated very low susceptibilities. The obvious strain differences could be expressed in terms of comparative indices of promoting effects of 2‐AAF and PB as well as DEN itself regarding each of the 8 strains tested. The use of F344 rats for the bioassay model was validated by the relatively high sensitivity to both DEN and 2‐AAF initiation as well as second‐stage promotion stimulus exhibited.
DOI:
10.1093/jnci/70.5.931
发表时间:
1983-05
期刊:
Journal of the National Cancer Institute
影响因子:
--
作者:
A. Malkinson;D. S. Beer
通讯作者:
A. Malkinson;D. S. Beer
DOI:
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发表时间:
1983
期刊:
Journal of the National Cancer Institute
影响因子:
--
作者:
Moore,CJ;Bachhuber,AJ;Gould,MN
通讯作者:
Gould,MN
影响因子:
11.2
作者:
Farber,E
通讯作者:
Farber,E