Liver Tumor Promotion by β-Naphthoflavone, a Strong CYP 1A1/2 Inducer, in a 28 Week Two-stage Rat Hepatocarcinogenesis Model Using Diethylnitrosamine as an Initiator
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概要
- 論文の詳細を見る
β-naphthoflavone (BNF) is a non-genotoxic, strong inducer of cytochrome P450 (CYP) 1A but not CYP 2B. In order to determine its liver tumor promotion potential, groups of male F344 rats were initiated with a single intraperitoneal injection of 200 mg/kg of diethylnitrosamine (DEN) and starting two weeks later, given 1% BNF (n=12) or non-supplemented diet (n=13) for 26 weeks. All animals were subjected to two-thirds partial hepatectomy at week 3. At sacrifice, absolute and relative liver weights in the DEN + BNF group showed statistically significant increase as compared to the DEN-alone group. The incidence of hepatocellular adenomas and numbers of such tumors and altered hepatocellular foci, positive for glutathione S-transferase placental form (GST-P), were also elevated. However, five animals given BNF alone without DEN initiation exhibited no focal hepatocellular lesions including GST-P positive foci. The numbers and areas of connexin 32 (Cx32)-positive spots per hepatocyte in centrilobular areas, and within altered hepatocellular foci and hepatocellular adenomas of the DEN + BNF group were significantly lower than those of the DEN-alone group. Immunohistochemically, CYP 1A1/2 was stained diffusely in the livers of the DEN + BNF group, but hepatocellular adenomas and some altered hepatocellular foci were generally negative. Proliferating cell nuclear antigen (PCNA) labeling indices of surrounding hepatocytes in the DEN + BNF group was about twice that of DEN-alone group, but the difference did not achive statistical significance. In the altered hepatocellular foci and adenomas of DEN + BNF group, the PCNA labeling indices were significantly higher than those of surrounding hepatocytes. These results indicate that BNF, a strong CYP 1A but not CYP 2B inducer, promote hepatocarcinogenesis initiated by DEN.
- 日本毒性病理学会の論文
- 1999-09-01
著者
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SHODA Toshiyuki
Toxicology Research Laboratories, Central Pharmaceutical Research Institute
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MITSUMORI Kunitoshi
Division of Pathology, National Institute of Health Sciences
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YAMAZAKI Yuji
Toxicology Research Lab., Central Pharmaceutical Research Institute, JAPAN TOBACCO INC.
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Yamazaki Yuji
Toxicology Research Lab. Central Pharmaceutical Research Institute Japan Tobacco Inc.
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Mitsumori Kunitoshi
Division Of Pathology National Institute Of Health Sciences
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Shoda Toshiyuki
Division of Pathology, Biological Safety Research Center National Institute of Health Sciences
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TAKAHASHI Tadakazu
Toxicology Research Laboratories, Central Pharmaceutical Research Institute, JAPAN TOBACCO INC.
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TAKAHASHI Tadakazu
Section of Safety, Research Laboratories, Torii Pharmaceutical Co., Ltd.
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HORIUCHI Ken-ichi
Section of Safety, Research Laboratories, Torii Pharmaceutical Co., Ltd.
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YAMAZAKI Yuji
Section of Safety, Research Laboratories, Torii Pharmaceutical Co., Ltd.
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SUZUKI Yusuke
Section of Safety, Research Laboratories, Torii Pharmaceutical Co., Ltd.
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KATSUDA Yoshiaki
Section of Safety, Research Laboratories, Torii Pharmaceutical Co., Ltd.
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YOKOMOTO Yasuki
Section of Safety, Research Laboratories, Torii Pharmaceutical Co., Ltd.
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KURUMI Masateru
Section of Safety, Research Laboratories, Torii Pharmaceutical Co., Ltd.
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Suzuki Yuusuke
Toxicology Research Laboratories Central Pharmaceutical Research Institute Japan Tobacco Inc.
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Horiuchi Ken-ichi
Section Of Safety Research Laboratories Torii Pharmaceutical Co. Ltd.
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Shoda Toshiyuki
Division Of Pathology National Institute Of Health Sciences
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Kurumi Masateru
Section Of Safety Research Laboratories Torii Pharmaceutical Co. Ltd.
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Yokomoto Yasuki
Section Of Safety Research Laboratories Torii Pharmaceutical Co. Ltd.
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Katsuda Yoshiaki
Section Of Safety Research Laboratories Torii Pharmaceutical Co. Ltd.
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Takahashi Tadakazu
Toxicology Research Laboratories Central Pharmaceutical Research Institute Japan Tobacco Inc.
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