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四氯化碳抑制大鼠肝细胞色素P450同工酶的研究 被引量:4

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出处 《卫生毒理学杂志》 CSCD 2000年第4期214-215,共2页 Journal of Health Toxicology
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  • 1[1] Chaudhury S, Mehendale HM. Amplification of CCl4 toxicity by chlordecone: Destruction of rat Hepatic microsomal cytochrome P-450 subpopulation, J Toxicol Environ Health, 1991, 32:277-294.
  • 2[2] Degawa M, Ohta A, Namiki M, et al. In vivo selection of a low spin form of cytochrome P-448 from 3-methylcholanthrene-induced rat cytochrome P-450 isozymes by carbon tetrachloride Biochem Pharmacol, 1987, 36:3315-3317.
  • 3[3] Degawa M, Mikami K, Mamiki M, et al. Inhibition of the induction and activity of hepatic P-450IA1 isozymes by in vivo administration of carbon tetrachloride to rats. Biol Pharm Bull,1993,16:1248-1250.
  • 4[4] Lubet RA, Mayer RT, Cameron JW, et al. Dealkylation of penotoxyresorufin:A rapid and sensitive assay for measuring induction of cytochrome P-450 by phenobarbital and other xenobiotics in the rat. Arch Biochem Biophys, 1985, 238:43-48.
  • 5[5] Manno M, DeMatteis F, Laurence JK. The mechanism of the suicidal, reductive inactivation of microsomal cytochrome P-450 by carbon tetrachloride. Biochem Pharmacol,1988,37:1981-1990.
  • 6[6] Balver WG, Boersma MG, Vaeger C,et al.Differential cumene hydroperoxide sensitivity of cytochrome P-450 enzymes I Al and IIB1 determined by their way & membrane incorporation, Biochimica et Biophysica Acta,1992,1117:179-187.

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