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Cancer Lett ; 151(1): 71-80, 2000 Apr 03.
Artigo em Inglês | MEDLINE | ID: mdl-10766425

RESUMO

Exposure of males to some genotoxic chemicals causes DNA damage in spermatozoa resulting in embryotoxicity and developmental defects in their offspring. This study demonstrates that cisplatin-DNA adducts could be measured in spermatozoa following treatment with the antineoplastic drug, cisplatin. The formation of spermatozoa cisplatin-DNA adducts showed dose and time-dependent increases both in vitro, and in vivo up to 168 h (7 days) after dosing. Treatment of rats with 10 mg cisplatin/kg resulted in spermatozoa Pt-GG adduct levels of approximately 1.0 fmol/microg DNA. When cisplatin-treated male rats were bred to untreated females 6-24 h after cisplatin administration, no adverse developmental effects or decreases in body weight were seen in the offspring although there was a trend towards increased early embryo mortality.


Assuntos
Cisplatino/metabolismo , Cisplatino/toxicidade , Adutos de DNA/metabolismo , Desenvolvimento Embrionário e Fetal/efeitos dos fármacos , Espermatozoides/fisiologia , Animais , Peso Corporal/efeitos dos fármacos , Dano ao DNA , Feminino , Morte Fetal/induzido quimicamente , Masculino , Gravidez , Ratos , Ratos Wistar , Espermatozoides/efeitos dos fármacos
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