Genotoxic potential of β-carbolines: A review

C. de Meester
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引用次数: 98

Abstract

The mutagenic and co-mutagenic properties of harman, norharman and of some of their pharmacologically important derivatives are reviewed. These compounds do not behave as true mutagens, but rather interact, directly or indirectly with DNA, leading to various consequences. This unusual behaviour is most probably related to the particular structure of the chemical nucleus common to all β-carbolines which confers to the different derivatives the property to interact with various macromolecules and enzymatic systems. These interactions are compiled and discussed in this review.

The alterations, by β-carbolines, of some important enzymatic systems, e.g. cytochrome P-450, have been clearly demonstrated, yet many discrepancies and contradictions exist so that an interpretation of the results and the definition of some common mechanism appears premature.

Since β-carbolines are widely distributed in tissues and since they may modify and increase genotoxic and toxic consequences of other compounds, these interactions need to be clarified.

β-卡波林的基因毒性潜力:综述
综述了骆驼蓬、去甲骆驼蓬及其一些重要药理衍生物的致突变性和共致突变性。这些化合物并不是真正的诱变剂,而是直接或间接地与DNA相互作用,导致各种后果。这种不寻常的行为很可能与所有β-卡波林共有的化学核的特殊结构有关,这赋予了不同衍生物与各种大分子和酶系统相互作用的特性。这些交互作用在本综述中进行了汇编和讨论。β-卡波林对一些重要酶系统(如细胞色素P-450)的改变已得到明确证明,但存在许多差异和矛盾,因此对结果的解释和某些常见机制的定义似乎为时过早。由于β-碳啉广泛分布在组织中,并且它们可能改变和增加其他化合物的遗传毒性和毒性后果,因此需要澄清这些相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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