Genetic Toxicity Study of YH1715 Series, Antifungal Agents

YH1715계열 항진균제의 유전독성평가

  • 하광원 (식품의약안전청 독성연구소 유전독성과) ;
  • 오혜영 (식품의약안전청 독성연구소 유전독성과) ;
  • 박장환 (식품의약안전청 독성연구소 유전독성과) ;
  • 허옥순 (식품의약안전청 독성연구소 유전독성과) ;
  • 손수정 (식품의약안전청 독성연구소 유전독성과) ;
  • 한의식 (식품의약안전청 독성연구소 유전독성과) ;
  • 이종영 (식품의약안전청 독성연구소 유전독성과) ;
  • 김소희 (식품의약안전청 독성연구소 유전독성과) ;
  • 강희일 (유한양행 중앙연구소)
  • Published : 1998.09.01

Abstract

The results of chromosome aberration test in mammalian cells in culture (Chinese hamster lung fibroblast cells) showed no induction of structural and numerical aberrations by antifungal agents of YH1715 series regardless of metabolic activation. While positive control group (mitomycin C and benzo(a)pyrene) showed structural chromosome aberrations of 37% and 23%, respectively. The in vivo induction of micronuclei was measured in polychromatic erythrocytes in bone marrow of male ddY mouse given YH1715R and YH1729R at 1, 0.5, 0.25 g/kg by p.o. once. After 24 hours, animals were sacrificed and evaluated 40 the incidence of micronucleated polychromatic erythrocytes in whole erythrocytes. Although a positive response for induction of micronuclei in animals treated with mitomycin C demonstrated the sensitivity of the test system for detection of a chemical clastogen, YH1715R did not induce micronuclei in bone marrow of ddY male mice but induced cytotoxicity to bone marrow cells at the highest concentration (1 g/kg, p〈0.05), and YH1729R induced micronuclei in bone marrow of ddY male mice dose dependently (p<0.05) but did not induce cytotoxicity to bone marrow cells.

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