J Korean Neuropsychiatr Assoc.  2000 May;39(3):629-637.

Genetic Safety Study of Chlorpromazine

Affiliations
  • 1National Bukog Mental Hospital, Bukog, Korea.
  • 2Department of Psychiatry, College of Medicine, Dongguk University, Kyungju, Korea.
  • 3Department of Pharmacology, College of Medicine, Dongguk University, Kyungju, Korea.

Abstract

OBJECT: The aim of this study is to determine whether exposure to chlorpromazine causes mutagenicity and genetic disorders. METHOD: Ames (Salmonella typhimurium) test and Rec assay (Bacillus subtilis) were used as indicators for DNA damage. Furthermore, the levels of umu operon expression by measuring the beta-galactosidase activity were monitered with the SOS umu test using S. typhimurium 1535 containing plasmid pSK1002. And the host-mediated assay was used to investigate the muta-genicity of chlorpromazine after the activation with in vivo metabolic systems.
RESULTS
From the results, chlorpromazine did not affect DNA of S. typhimurium and B. subtilis strains and showed no mutagenicity at the all concentrations tested. These phenomena was also similar to that after metabolic activation of chlorpromazine in in vivo system.
CONCLUSION
These results suggested that chlorpromazine did not show the mutagenicity and genotoxicity by four different methods used in this study.

Keyword

Chlorpromazine; Ames test; Recassay; SOS umu test; Host-mediated assay

MeSH Terms

beta-Galactosidase
Biotransformation
Chlorpromazine*
DNA
DNA Damage
Operon
Plasmids
Chlorpromazine
DNA
beta-Galactosidase
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