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人肝脏微粒体中CYP2B6对异丙酚代谢的催化作用 被引量:1

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摘要 异丙酚是一种广泛应用于临床的短效静脉麻醉药,在人体内其生物转化途径主要有两条:在肝脏内进行葡萄糖醛酸化和羟基化,后者主要由CYP酶系催化,约代谢异丙酚总量的40%。由于药物的相互作用大多是竞争相同CYP的结果,异丙酚常与其它麻醉药复合使用,异丙酚可影响其他药物的代谢,所以阐明催化异丙酚代谢的具体CYP酶对预测异丙酚的临床药代动力学、药效学特性很重要。
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 2007年第5期475-476,共2页 Chinese Journal of Anesthesiology
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  • 1Favetta P, Degoute CS, Perdrix JP, et al. Propofol metabolites in man following propofol induction and maintenance. Br J Anaesth, 2002, 88: 653-658.
  • 2Hamaoka N, Oda Y, Hase I, et al. Propofol decreases the clearance of midazolam by inhibiting CYP3A4: an in vivo and in vitro study . Clin Pharmacol Ther, 1999,66: 110-117.
  • 3Inomata S, Nagashima A, Osaka Y, et al. Propofol inhibits lidocaine metabolism in human and rat liver microsomes. J Anesth, 2003, 17: 246-250.
  • 4Court MH, Duan SX, Hesse LM, et al. Cytoehrome P-450 2B6 is responsible for interindividual variability of propofol hydroxylation by human liver mierosomes. Anesthesiology, 2001,94 : 110-119.
  • 5Guitton J, Buronfosse T, Desage M, et al. Possible involvement of multiple human cytochrome P450 isoforms in the liver metabolism of propofol. Br J Anaesth, 1998,80: 788-795.
  • 6Hijazi Y, Boulieu R. Contribution of CYP3A4, CYP2B6, and CYP2C9 isoforms to N-demethylation of ketamine in human liver mierosomes. Drug Metab Dispos, 2002,30: 853-858.
  • 7Tanaka E, Takano Y, Inomata S, et al. Premedication medicines do not cause drug metabolic interaction with propofol using human liver mierosomes in vitro. Eur J Clin Pharmacol, 2004, 60: 565-568.
  • 8Faucette SR, Hawke RL, Lecluyse EL, et al. Validation of bupropion hydroxylation as a selective marker of human cytochrome P450 2B6 catalytic activity. Drug Metab Dispos, 2000, 28,1222-1230.
  • 9Richter T, Schwab M, Eichelbaum M, et al. Inhibition of human CYP2B6 by N, N', N”-triethylenethiophosphoramide is irreversible and mechanlsm-based. Biochem Pharmacol, 2005, 69: 517-524.
  • 10Lamba V, Lamba J, Yasuda K, et al. Hepatic CYP2B6 expression: gender and ethnic differences and relationship to CYP2B6 genotype and CAR (constitutive androstane receptor) expression. J Pharmacol Exp Ther, 2003,307: 906-922.

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