1992
DOI: 10.1016/0003-9861(92)90271-w
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Tissue-specific expression, induction, and inhibition through metabolic intermediate-complex formation of guinea pig cytochrome P450 belonging to the CYP2B subfamily

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Cited by 10 publications
(11 citation statements)
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“…To clarify the mechanism whereby PB increases CYP2B expression, it would be useful to focus on such differences and mutant animal models. Thus, we examined the genomic sequences of the guinea pig, a species less responsive to PB [15,16], and the Qdj:SD rat, a mutant strain lacking inducible expression of the CYP2B2 gene [174]. The results obtained show that there is no PBREM 5'-upstream of the guinea pig CYP2B18 gene [175], which agrees with the importance of PBREM in obtaining a PB-response.…”
Section: Xenobiotic Regulation Of Cyp2b Expre-ssionsupporting
confidence: 80%
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“…To clarify the mechanism whereby PB increases CYP2B expression, it would be useful to focus on such differences and mutant animal models. Thus, we examined the genomic sequences of the guinea pig, a species less responsive to PB [15,16], and the Qdj:SD rat, a mutant strain lacking inducible expression of the CYP2B2 gene [174]. The results obtained show that there is no PBREM 5'-upstream of the guinea pig CYP2B18 gene [175], which agrees with the importance of PBREM in obtaining a PB-response.…”
Section: Xenobiotic Regulation Of Cyp2b Expre-ssionsupporting
confidence: 80%
“…Furthermore, the ability to metabolize strychnine differs from species to species. Such a difference in strychnine metabolism is correlated with the expression level of CYP2B isozymes in each species [14][15][16]. These observations suggest that animals expressing highly-inducible CYP2Bs are more tolerant of the toxic effects of strychnine than other species with poorly-inducible enzymes.…”
Section: Induction Of Cyp2b: Its Evolutional Significancementioning
confidence: 83%
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“…Many of the above named drugs are subject to cytochrome P450‐mediated drug oxidation ( Jurima‐Romet et al ., 1993 , Stearns et al ., 1995 , Oldham et al ., 1997 , Tracy et al ., 1999 ), but surprisingly, little is known about the metabolic capacity of the heart. Indeed, there is very limited information on the expression of P450 isozymes in heart tissue of laboratory animals ( Stegeman et al ., 1982 , Geetha et al ., 1991 , Yamada et al ., 1992 , McCallum et al ., 1993 , Fulton et al ., 1995 , Xiao et al ., 1998 ) despite their importance in the metabolism of drugs.…”
Section: Introductionmentioning
confidence: 99%
“…Interestingly, coadministration of a-tocopherol reduced signi® cantly the alteration observed in microsomes of rat heart tissue. The tissue-speci® c expression, induction and inhibition through metabolic intermediate complex formation of guinea pig P450 was studied by Yamada et al (1992). They reported that treatment with dexamethasone or p,p« -dichlorodiphenyltrichloroethane and}or isoafrole produced very signi® cant induction in the expression of P450 isozymes in guinea pig heart tissue.…”
Section: Cytochrome P450 (P450) System In Cardiomyocytesmentioning
confidence: 99%