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对乙酰氨基酚在小鼠体内的肝毒性和代谢的时间变化

Temporal variation in hepatotoxicity and metabolism of acetaminophen in mice.

作者信息

Kim Y C, Lee S J

机构信息

College of Pharmacy, Seoul National University, South Korea.

出版信息

Toxicology. 1998 Jun 26;128(1):53-61. doi: 10.1016/s0300-483x(98)00046-8.

Abstract

Temporal variation in metabolism and hepatotoxicity of acetaminophen (APAP) was examined using male ICR mice. Animals were injected with a single dose of APAP (400 mg/kg, i.p.) at 08:00, 14:00 or 20:00 h. APAP at this dose was markedly hepatotoxic to mice when administered at 20:00 h as determined by increases in serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities, and by decreases in hepatic glucose-6-phosphatase (G-6-Pase) activity. However, mice appeared to be entirely insensitive to an identical dose of APAP given either at 08:00 or 14:00 h. Hepatic glutathione (GSH) level was significantly higher at 08:00, but no difference in GSH levels between 14:00 and 20:00 h was observed in normal mice. APAP and its metabolites in blood were monitored using HPLC for 3 h following the treatment. There were no significant differences in the plasma concentrations of APAP, APAP-glucuronide, APAP-sulfate, or APAP-mercapturate among the mice treated with this drug at 08:00, 14:00 or 20:00 h. However, the APAP-cysteine and APAP-GSH levels measured at 1 h following the APAP treatment were significantly lower in mice treated with this analgesic either at 14:00 or 20:00 h. In vitro hepatic microsomal p-nitrophenol hydroxylase activities were not different between 08:00, 14:00 and 20:00 h. But ethoxyresorufin O-deethylase and aminopyrine N-demethylase activities measured at 14:00 h were significantly lower than those of 08:00 or 20:00 h. Thus, the greater hepatotoxicity of APAP administered at 20:00 h appears to be related to the marked decrease in hepatic GSH at this time period, whereas the simultaneous reduction in APAP activation may be responsible for the lack of hepatotoxicity in mice treated with this analgesic at 14:00 h. These results suggest that the temporal variation in hepatotoxicity and metabolism of APAP is determined by interactions of multiple factors including the hepatic GSH level and drug metabolizing activities.

摘要

利用雄性ICR小鼠研究了对乙酰氨基酚(APAP)代谢和肝毒性的时间变化。在08:00、14:00或20:00给动物腹腔注射单剂量APAP(400mg/kg)。当在20:00给药时,该剂量的APAP对小鼠具有明显的肝毒性,这可通过血清丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)活性的升高以及肝葡萄糖-6-磷酸酶(G-6-Pase)活性的降低来确定。然而,小鼠对在08:00或14:00给予的相同剂量的APAP似乎完全不敏感。正常小鼠的肝谷胱甘肽(GSH)水平在08:00时显著更高,但在14:00和20:00之间未观察到GSH水平的差异。给药后3小时使用高效液相色谱法监测血液中的APAP及其代谢产物。在08:00、14:00或20:00用该药物治疗的小鼠中,APAP、APAP-葡萄糖醛酸苷、APAP-硫酸盐或APAP-巯基尿酸盐的血浆浓度没有显著差异。然而,在APAP治疗后1小时测得的APAP-半胱氨酸和APAP-GSH水平在14:00或20:00用该镇痛药治疗的小鼠中显著更低。08:00、14:00和20:00之间的体外肝微粒体对硝基苯酚羟化酶活性没有差异。但在14:00测得的乙氧基异吩恶唑酮O-脱乙基酶和氨基比林N-脱甲基酶活性显著低于08:00或20:00时的活性。因此,20:00给予的APAP更大的肝毒性似乎与该时间段肝GSH的显著降低有关,而APAP活化的同时降低可能是14:00用该镇痛药治疗的小鼠缺乏肝毒性的原因。这些结果表明,APAP肝毒性和代谢的时间变化是由包括肝GSH水平和药物代谢活性在内的多种因素的相互作用决定的。

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