Comparative mutagenic and genotoxic effects of three antimalarial drugs, chloroquine, primaquine and amodiaquine
Author(s) -
Taraknath Chatterjee,
Amitabha Muhkopadhyay,
K.A. Khan,
Ashok K. Giri
Publication year - 1998
Publication title -
mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.723
H-Index - 91
eISSN - 1464-3804
pISSN - 0267-8357
DOI - 10.1093/mutage/13.6.619
Subject(s) - amodiaquine , primaquine , sister chromatid exchange , chloroquine , in vivo , pharmacology , ames test , chemistry , genotoxicity , chromosome aberration , salmonella , malaria , biology , in vitro , toxicity , biochemistry , chromosome , immunology , genetics , organic chemistry , bacteria , gene
Comparative mutagenic and genotoxic effects of three antimalarial drugs, chloroquine, primaquine and amodiaquine, were assessed in the Ames mutagenicity assay (in strains TA97a, TA100, TA102 and TA104) and in vivo sister chromatid exchange (SCE) and chromosome aberration (CA) assays in bone marrow cells of mice. These are the most commonly used antimalarial drugs available at present throughout the world. The results of the bacterial mutagenicity assays showed a very weak mutagenic effect of all three drugs in Salmonella strains TA97a and TA100 both with and without S9 mix and in TA104 only with S9 mix. The results of the in vivo SCE and CA assays indicate that these three drugs are genotoxic in bone marrow cells of mice.
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