Your browser doesn't support javascript.
loading
Metabolic activation of o-phenylphenol to a major cytotoxic metabolite, phenylhydroquinone: role of human CYP1A2 and rat CYP2C11/CYP2E1.
Ozawa, S; Ohta, K; Miyajima, A; Kurebayashi, H; Sunouchi, M; Shimizu, M; Murayama, N; Matsumoto, Y; Fukuoka, M; Ohno, Y.
Afiliación
  • Ozawa S; Division of Pharmacology, National Institute of Health Sciences, Tokyo, Japan. sozawa@nihs.go.jp
Xenobiotica ; 30(10): 1005-17, 2000 Oct.
Article en En | MEDLINE | ID: mdl-11315102
1. The in vitro metabolic activation of o-phenylphenol has been evaluated as yielding a toxic metabolite, 2,5-dihydroxybiphenyl (phenylhydroquinone), by p-hydroxylation in liver microsomes of rat and human. The involvement of rat CYP2C11, CYP2E1 and human CYP1A2 in the p-hydroxylation of o-phenylphenol is suggested. 2. 2,3- and phenylhydroquinone, which induced DNA single-strand scission in the presence of 1 microM CuCl2, were the most cytotoxic chemicals examined to cultured mammalian cell lines among o-phenylphenol, m-phenylphenol, p-phenylphenol, 2,2'-, 4,4'-, 2,3- and phenylhydroquinone. 3. Rat and human liver microsomes catalysed the formation of phenylhydroquinone, but not 2,3-dihydroxybiphenyl, using o-phenylphenol as a substrate. A higher rate of metabolic activation of o-phenylphenol was observed with livers of the male than the female rats by 5.6- and 2.6-fold respectively. 4. Inhibitory antibodies against the male-specific CYP2C11 inhibited hepatic o-phenylphenol p-hydroxylation in the male F344 and Sprague-Dawley rat by > 70%. Liver microsomes from the isoniazid-treated rats produced 1.8- and 3-fold induction of o-phenylphenol p-hydroxylation and chlorzoxazone 6-hydroxylation (a CYP2E1-dependent activity) respectively. 5. Human CYP1A2, expressed by baculovirus-mediated cDNA expression systems, exhibited a remarkably higher capacity for o-phenylphenol p-hydroxylation at concentrations of 5 (> 5-fold), 50 (> 2-fold) and 500 microM (> 2-fold) than CYP2A, CYP2B, CYP2Cs, CYP2D6, CYP2E1 and CYP3A4 on the basis of pmol P450. 6. Among various CYP inhibitors tested here, 7,8-benzoflavone and furafylline, typical human CYP1A2 inhibitors, inhibited the microsomal p-hydroxylation of o-phenylphenol in human livers most potently by 70 and 50% respectively. 7. The results thus indicate the involvement of rat CYP2C11/CYP2E1 and human CYP1A2 in the hepatic p-hydroxylation of o-phenylphenol.
Asunto(s)
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenoles / Polímeros / Esteroide Hidroxilasas / Flavonoides / Compuestos de Bifenilo / Microsomas Hepáticos / Hidrocarburo de Aril Hidroxilasas / Citocromo P-450 CYP1A2 / Citocromo P-450 CYP2E1 / Sistema Enzimático del Citocromo P-450 Límite: Animals / Humans / Male Idioma: En Revista: Xenobiotica Año: 2000 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenoles / Polímeros / Esteroide Hidroxilasas / Flavonoides / Compuestos de Bifenilo / Microsomas Hepáticos / Hidrocarburo de Aril Hidroxilasas / Citocromo P-450 CYP1A2 / Citocromo P-450 CYP2E1 / Sistema Enzimático del Citocromo P-450 Límite: Animals / Humans / Male Idioma: En Revista: Xenobiotica Año: 2000 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido