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四氯化碳预处理的雄性小鼠中对乙酰氨基酚I期和II期代谢的对比变化。

Contrasting changes in phase I and phase II metabolism of acetaminophen in male mice pretreated with carbon tetrachloride.

作者信息

Yim Hye K, Jung Young S, Kim Sung Y, Kim Young C

机构信息

College of Pharmacy, Seoul National University, San 56-1 Shinrim-Dong, Kwanak-Ku, Seoul, Korea.

出版信息

Basic Clin Pharmacol Toxicol. 2006 Feb;98(2):225-30. doi: 10.1111/j.1742-7843.2006.pto_308.x.

Abstract

Effect of carbon tetrachloride (CCl(4)) pretreatment on the biotransformation and elimination of acetaminophen were examined in male mice. A 24 hr initial dose of CCl(4) (0.05 ml/kg, intraperitioneally) reduced the induction of hepatotoxicity resulting from acetaminophen treatment (350 mg/kg, intraperitoneally) as determined by changes in serum alanine and aspartate aminotransferase, and sorbitol dehydrogenase activities. Acetaminophen and the major metabolites in plasma were monitored for 12 hr following acetaminophen treatment. CCl(4) pretreatment decreased the plasma concentrations of acetaminophen-cysteine and acetaminophen-mercapturate, but acetaminophen-glucuronide and acetaminophen-sulfate were increased significantly. The elimination of the parent drug from plasma was not affected by CCl(4). In urine collected for 24 hr, the concentrations of acetaminophen-sulfate and acetaminophen-glucuronide were increased by 84% and 33%, respectively, whilst acetaminophen-cysteine and acetaminophen-mercapturate were reduced to approximately one third of control. Expression of cytochrome P450 (CYP) isozymes was determined using antibodies of 2E1 and 1A2 as probes. CYP2E1 and 1A2 expressions were decreased significantly by CCl(4). Likewise, CCl(4) treatment reduced the microsomal p-nitrophenol hydroxylase and p-nitroanisole O-demethylase activities to less than one third of control. The results indicate that, although CCl(4) reduces the generation of thioether conjugates of acetaminophen by decreasing the CYP activities, inhibition of the oxidative metabolism of acetaminophen is counterbalanced by the enhancement of conjugate formation via the glucuronide and sulfate pathways, resulting in elimination of the drug at a rate equivalent to that in normal mice. It is suggested that liver injury in patients may not warrant a mandatory reduction of drug doses extensively inactivated via phase II reactions.

摘要

在雄性小鼠中研究了四氯化碳(CCl₄)预处理对乙酰氨基酚生物转化和消除的影响。经24小时的初始剂量CCl₄(0.05毫升/千克,腹腔注射)处理后,由乙酰氨基酚治疗(350毫克/千克,腹腔注射)导致的肝毒性诱导作用减弱,这可通过血清丙氨酸和天冬氨酸转氨酶以及山梨醇脱氢酶活性的变化来确定。在乙酰氨基酚治疗后12小时监测血浆中的乙酰氨基酚及其主要代谢产物。CCl₄预处理降低了乙酰氨基酚 - 半胱氨酸和乙酰氨基酚 - 巯基尿酸盐的血浆浓度,但乙酰氨基酚 - 葡萄糖醛酸苷和乙酰氨基酚 - 硫酸盐显著增加。母体药物从血浆中的消除不受CCl₄影响。在收集24小时的尿液中,乙酰氨基酚 - 硫酸盐和乙酰氨基酚 - 葡萄糖醛酸苷的浓度分别增加了84%和33%,而乙酰氨基酚 - 半胱氨酸和乙酰氨基酚 - 巯基尿酸盐降至对照的约三分之一。使用2E1和1A2抗体作为探针测定细胞色素P450(CYP)同工酶的表达。CCl₄显著降低了CYP2E1和1A2的表达。同样,CCl₄处理使微粒体对硝基苯酚羟化酶和对硝基苯甲醚O - 脱甲基酶活性降低至对照的不到三分之一。结果表明,尽管CCl₄通过降低CYP活性减少了乙酰氨基酚硫醚共轭物的生成,但通过葡萄糖醛酸苷和硫酸盐途径共轭物形成的增强抵消了乙酰氨基酚氧化代谢的抑制作用,导致药物以与正常小鼠相当的速率消除。提示对于通过II相反应广泛失活的药物,患者的肝损伤可能不一定需要强制大幅降低药物剂量。

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