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中药对 dexamethasone 诱导的细胞色素 P450 介导的黄曲霉毒素 B1 致突变性及代谢的抑制作用

Inhibition of dexamethasone-induced cytochrome P450-mediated mutagenicity and metabolism of aflatoxin B1 by Chinese medicinal herbs.

作者信息

Wong B Y, Lau B H, Yamasaki T, Teel R W

机构信息

Department of Natural Science, Graduate School, Loma Linda University, CA 92350.

出版信息

Eur J Cancer Prev. 1993 Jul;2(4):351-6. doi: 10.1097/00008469-199307000-00010.

Abstract

Oldenlandia diffusa (OD) and Scutellaria barbata (SB) have been used in traditional Chinese medicine for treating liver, lung and rectal tumours. We previously showed that they inhibited mutagenesis, DNA binding and metabolism of aflatoxin B1 (AFB1) and benzo(a)pyrene (BaP) bioactivated by Aroclor 1254-induced rat S9. The purpose of this study was to investigate the effects of OD and SB on the mutagenicity of AFB1 in Salmonella typhimurium TA100 using dexamethasone (DXM)-induced rat hepatic S9, on cytochrome P450-linked aminopyrine N-demethylase (APND) activity in DXM-induced hepatic microsomes and on the metabolism of AFB1 by DXM-induced S9 using high-performance liquid chromatography (HPLC). The experimental results showed that OD and SB consistently inhibited the mutagenicity of AFB1 bioactivated by either non-induced or DXM-induced S9. These effects correlated with the inhibition of cytochrome P450-linked APND activity in DXM-induced microsomes and with an inhibition of DXM-induced S9 mediated metabolism of [3H]AFB1 as determined by HPLC. Since DXM treatment has been associated with an induction of the CYP3 enzyme family, these results suggest that OD and SB may possess antimutagenic and antitumorigenic activity towards AFB1 through an inhibition of CYP3-mediated metabolism of AFB1.

摘要

白花蛇舌草(OD)和半枝莲(SB)在传统中药中用于治疗肝脏、肺部和直肠肿瘤。我们之前表明,它们能抑制由Aroclor 1254诱导的大鼠S9生物活化的黄曲霉毒素B1(AFB1)和苯并(a)芘(BaP)的诱变、DNA结合及代谢。本研究的目的是使用地塞米松(DXM)诱导的大鼠肝脏S9,研究OD和SB对鼠伤寒沙门氏菌TA100中AFB1诱变性的影响,对DXM诱导的肝微粒体中细胞色素P450相关的氨基比林N-脱甲基酶(APND)活性的影响,以及使用高效液相色谱法(HPLC)研究DXM诱导的S9对AFB1代谢的影响。实验结果表明,OD和SB始终抑制未诱导或DXM诱导的S9生物活化的AFB1的诱变性。这些作用与DXM诱导的微粒体中细胞色素P450相关的APND活性的抑制以及HPLC测定的DXM诱导的S9介导的[3H]AFB1代谢的抑制相关。由于DXM处理与CYP3酶家族的诱导有关,这些结果表明,OD和SB可能通过抑制CYP3介导的AFB1代谢而对AFB1具有抗诱变和抗肿瘤活性。

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