MUTAGENICITY STUDIES OF PREDNISOLONE FARNESYLATE (PNF)

Prednisolone farnesylate (PNF) was tested for mutagenicity by Ames test using Salmonella typhimurium (TAl00, TA1535, TA98, TA1537) and Escherichia coli (WP2 uvrA), for clastogenic activity in vitro by the chromosomal aberration test in a Chinese hamster fibroblast cell line (CHL), and for induction...

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Published inJournal of toxicological sciences Vol. 17; no. SupplementIII; pp. 269 - 281
Main Authors OTSUKA, Masanori, AJIMI, Shozo, KAJIWARA, Yoshitsugu, OGURA, Shozo, KAKIMOTO, Keijiro, INAI, Tsunehiko, TANAKA, Hidetsugu, OHUCHIDA, Akinobu
Format Journal Article
LanguageEnglish
Published Suita The Japanese Society of Toxicology 01.01.1992
Japan Science and Technology Agency
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Abstract Prednisolone farnesylate (PNF) was tested for mutagenicity by Ames test using Salmonella typhimurium (TAl00, TA1535, TA98, TA1537) and Escherichia coli (WP2 uvrA), for clastogenic activity in vitro by the chromosomal aberration test in a Chinese hamster fibroblast cell line (CHL), and for induction of micronuclei by the micronucleus test in male ICR mice. 1) In Ames test, PNF with and without metabolic activation showed no mutagenicity in any strains at any dose levels (312∼5, 000 μg/plate). 2) In the chromosomal aberration test, PNF with metabolic activation produced a slight increase in the incidence of structural chromosomal aberrations in CHL cells at l, 500 μg/ml. 3) In the micronucleus test, a single administration of PNF caused no significant increase of micronucleated polychromatic erythrocytes at any doses (250∼2, 000 mg/kg).
AbstractList Prednisolone farnesylate (PNF) was tested for mutagenicity by Ames test using Salmonella typhimurium (TAl00, TA1535, TA98, TA1537) and Escherichia coli (WP2 uvrA), for clastogenic activity in vitro by the chromosomal aberration test in a Chinese hamster fibroblast cell line (CHL), and for induction of micronuclei by the micronucleus test in male ICR mice. 1) In Ames test, PNF with and without metabolic activation showed no mutagenicity in any strains at any dose levels (312∼5, 000 μg/plate). 2) In the chromosomal aberration test, PNF with metabolic activation produced a slight increase in the incidence of structural chromosomal aberrations in CHL cells at l, 500 μg/ml. 3) In the micronucleus test, a single administration of PNF caused no significant increase of micronucleated polychromatic erythrocytes at any doses (250∼2, 000 mg/kg).
Author KAKIMOTO, Keijiro
OHUCHIDA, Akinobu
OGURA, Shozo
INAI, Tsunehiko
AJIMI, Shozo
OTSUKA, Masanori
KAJIWARA, Yoshitsugu
TANAKA, Hidetsugu
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CitedBy_id crossref_primary_10_1016_j_mrgentox_2021_503334
crossref_primary_10_1016_j_mrgentox_2007_02_004
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crossref_primary_10_1016_j_mrrev_2008_09_002
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References 石館 基 監修 (1983): 染色体異常試験データ集, 株式会社エル•アイ•シー.
Kastenbaum, M. A. and Bowman, K. O. (1970): Tables for determining the statistical significance of mutation frequencies. Mutation Res., 9, 527-549.
Schmid, W. (1976): The micronucleus test for cytogenetic analysis. In Chemical Mutagens, Principles and Methods for their Detection (A. Hollaender, ed.), vol. 4, p. 31-54. Plenum, New York
Mavournin, K. H., Blakey, D. H., Cimino, M. C., et al., (1990): The in vivo micronucleus assay in mammalian bone marrow and peripheral blood. A report of the U. S. environmental protection agency gene-tox program, Mutation Res., 239, 29-80.
Ames, B. N., McCann, J. and Yamasaki, E. (1975): Methods for detecting carcinogens and mutagens with the Salmonella/mammalian-microsome mutagenicity test. Mutation Res., 31, 347-364.
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Title MUTAGENICITY STUDIES OF PREDNISOLONE FARNESYLATE (PNF)
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