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局部涂抹粗煤焦油后,SENCAR小鼠表皮和肺中苯并(a)芘二醇环氧化物-I-DNA加合物的形成。

Benzo(a)pyrene diol epoxide-I-DNA adduct formation in the epidermis and lung of SENCAR mice following topical application of crude coal tar.

作者信息

Mukhtar H, Asokan P, Das M, Santella R M, Bickers D R

出版信息

Cancer Lett. 1986 Dec;33(3):287-94. doi: 10.1016/0304-3835(86)90068-6.

Abstract

The levels of benzo[a]pyrene diol epoxide-I-deoxyguanosine (BPDE-I-dG) adduct formation in epidermis and lung of SENCAR mice following the topical application of benzo[a]pyrene (BP) alone, crude coal tar (CCT) alone, and the two combined were determined in an enzyme linked immunosorbent (ELISA) assay using monoclonal antibodies. Topical application of two doses of BP (20 micrograms) at 72-h intervals, with sacrifice 24 h later resulted in the formation of 197 fmol and 205 fmol BPDE-I-dG adducts per mg DNA in epidermis and lung, respectively. Topical application of 0.5 ml CCT alone resulted in the formation of 278 fmol and 410 fmol BPDE-I-dG adducts per mg DNA in epidermis and lung, respectively. Simultaneous topical application of 20 micrograms BP and CCT (0.1-0.5 ml) resulted in substantially lower BPDE-I-dG adducts in the epidermis as well as in the lung. Our results suggest that CCT may contain inhibitors of carcinogen-DNA adduct formation and that topical application of CCT produces greater effects on DNA-adduct formation in lung than in epidermis. Thus the cancer-causing potency of the polycyclic aromatic hydrocarbons (PAHs) in CCT may be reduced by other anticarcinogenic constituents present in CCT and systemic absorption of carcinogenic PAHs in CCT applied to skin might have tumorigenic effects in other tissues.

摘要

采用单克隆抗体,通过酶联免疫吸附测定(ELISA)法,测定了单独局部涂抹苯并[a]芘(BP)、单独涂抹粗煤焦油(CCT)以及二者联合使用后,SENCAR小鼠表皮和肺中苯并[a]芘二醇环氧化物-I-脱氧鸟苷(BPDE-I-dG)加合物的形成水平。以72小时的间隔局部涂抹两剂BP(20微克),24小时后处死小鼠,结果显示表皮和肺中每毫克DNA分别形成197飞摩尔和205飞摩尔的BPDE-I-dG加合物。单独局部涂抹0.5毫升CCT,表皮和肺中每毫克DNA分别形成278飞摩尔和410飞摩尔的BPDE-I-dG加合物。同时局部涂抹20微克BP和CCT(0.1 - 0.5毫升),表皮和肺中的BPDE-I-dG加合物显著减少。我们的结果表明,CCT可能含有致癌物-DNA加合物形成的抑制剂,并且局部涂抹CCT对肺中DNA加合物形成的影响比对表皮的影响更大。因此,CCT中多环芳烃(PAHs)的致癌能力可能会被CCT中存在的其他抗癌成分降低,并且局部涂抹于皮肤的CCT中致癌PAHs的全身吸收可能会对其他组织产生致瘤作用。

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