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二烯丙基三硫化物对诱变剂在原代大鼠肝细胞中诱导DNA损伤合成的影响。

Effect of diallyl trisulfide on induction of UDS by mutagenic drugs in primary rat hepatocytes.

作者信息

Deng D J, Mueller K, Kasper P, Mueller L

机构信息

Beijing Institute for Cancer Research, China.

出版信息

Biomed Environ Sci. 1994 Mar;7(1):85-90.

PMID:8024723
Abstract

Most of anticancer drugs are mutagenic. A possible exception is diallyl trisulfide (DAT), a component of garlic. It is an antimutagenic anticancer chemical although it is mainly used as antibiotic. Its modifying effect on induction of UDS by mutagenic mitomycin C (MMC), cyclophosphamide (CP) and cis-diamine dichloroplatin (DDP) was investigated with the UDS assay in the primary cultures of Wistar rat hepatocytes (hpc) using the autoradiographic technique. Results showed that 1.0-4.0 nmol/ml of DAT did not induce UDS and that MMC, CP and DDP resulted in a significant induction of dose-dependent UDS. DAT enhanced induction of UDS by these drugs. A dose-effect relationship was observed between dose of DAT and enhancement of induction of UDS. However, the mechanism of the enhancement is not clear.

摘要

大多数抗癌药物具有致突变性。大蒜的成分二烯丙基三硫化物(DAT)可能是个例外。它是一种抗诱变的抗癌化学物质,尽管它主要用作抗生素。利用放射自显影技术,通过Wistar大鼠肝细胞原代培养物中的UDS测定法,研究了其对诱变剂丝裂霉素C(MMC)、环磷酰胺(CP)和顺二氯二氨铂(DDP)诱导UDS的修饰作用。结果表明,1.0 - 4.0 nmol/ml的DAT不诱导UDS,而MMC、CP和DDP可显著诱导剂量依赖性UDS。DAT增强了这些药物对UDS的诱导作用。在DAT剂量与UDS诱导增强之间观察到剂量效应关系。然而,增强机制尚不清楚。

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