氯丙嗪及相关吩噻嗪类药物的遗传毒性研究进展

Elmar Gocke
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引用次数: 64

摘要

氯丙嗪和相关的吩噻嗪类药物已在人类和兽药中使用了40多年,主要用作精神药物。遗传毒性报告在许多情况下是相对陈旧的试验设计。总的来说,在标准条件下测试时,似乎没有与这些药物相关的遗传毒性活性。有限的证据表明,潜在的形成诱变亚硝化产物和一些迹象表明,有能力调节基因毒性作用的各种诱变剂已在文献中提出。氯丙嗪和其他氯化衍生物的紫外线照射产生具有DNA损伤特性的活性自由基。在适当设计的光致突变实验中观察到基因突变和染色体畸变的诱导。氯丙嗪对紫外线诱导的皮肤肿瘤形成有增强作用,但也有减少作用。造成不同行动的决定性因素还没有被认识到。显然,建议在使用这些药物治疗期间避免广泛的紫外线照射。
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Review of the genotoxic properties of chlorpromazine and related phenothiazines

Chlorpromazine and related phenothiazine drugs have been used in human and veterinary medications for more than 40 years, predominantly as psychotropic agents. Genotoxicity reports are in many cases of relatively antiquated test design. Overall there appears to be no genotoxic activity associated with these drugs when tested under standard conditions. Limited evidence for the potential to form mutagenic nitrosation products and some indication for the ability to modulate the genotoxic action of various mutagens have been presented in the literature. UV irradiation of chlorpromazine and other chlorinated derivatives produces reactive free radicals which possess DNA damaging properties. Induction of gene mutation and chromosomal aberrations have been observed in appropriately designed photomutagenesis experiments. Enhancement but also reduction of UV induced skin tumour formation by chlorpromazine have been found. The decisive factor for the discrepant actions has not been recognized. It is clearly advisable to avoid extensive UV exposure during therapy with these drugs.

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DNA adducts and chronic degenerative diseases. Pathogenetic relevance and implications in preventive medicine Carbon tetrachloride: Genetic effects and other modes of action Dr. Hans F. Stich, Professor Emeritus of the University of British Columbia, 1927–1995 Product review Foreword
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