Cretton E M, Sommadossi J P
Department of Pharmacology, University of Alabama, Birmingham 35294.
Biochem Pharmacol. 1991 Sep 12;42(7):1475-80. doi: 10.1016/0006-2952(91)90461-d.
Metabolic studies of 3'-azido-3'-deoxythymidine (AZT) in humans have demonstrated that this compound is primarily eliminated as a 5'-O-glucuronide, 3'-azido-3'-deoxy-5'-beta-D-glucopyranuronosylthymidine (GAZT), accounting for approximately 80% of the administered dose. Recently, we characterized the complete catabolic pathway of AZT in freshly isolated rat hepatocytes in suspension, demonstrating extensive formation of three catabolites, including GAZT, 3'-amino-3'-deoxythymidine (AMT), and 3'-amino-3'-deoxy-5'-beta-D-glucopyranuronosylthymidine (GAMT). The present study evaluated the effects of probenecid (PROB) and acetaminophen (ACET), two agents which are also metabolized by UDP-glucuronyltransferase, on the metabolism and transmembrane distribution of AZT in rat hepatocytes. Pre-exposure of cells to 350 microM PROB 30 min prior to the addition of 10 microM [3H]AZT decreased intracellular GAZT levels by approximately 10-fold. Interestingly, AMT formation was enhanced approximately 1.5-fold in the presence of PROB, probably resulting from increased AZT availability. In contract, pre-exposure to 50 microM ACET 30 min prior to addition of 10 microM [3H]AZT did not substantially alter AZT glucuronidation. Additionally, decreased AZT catabolism by PROB did not contribute to the formation of 5'-phosphorylated derivatives of AZT. Agents which undergo glucuronidation may thus not necessarily affect AZT conversion to GAZT, and their potential interactions should be investigated using in vitro systems prior to co-administration with AZT.
对人类进行的3'-叠氮基-3'-脱氧胸苷(AZT)代谢研究表明,该化合物主要以5'-O-葡糖醛酸苷,即3'-叠氮基-3'-脱氧-5'-β-D-吡喃葡糖醛酸基胸苷(GAZT)的形式消除,约占给药剂量的80%。最近,我们对悬浮培养的新鲜分离大鼠肝细胞中AZT的完整分解代谢途径进行了表征,证明了三种分解代谢产物的大量形成,包括GAZT、3'-氨基-3'-脱氧胸苷(AMT)和3'-氨基-3'-脱氧-5'-β-D-吡喃葡糖醛酸基胸苷(GAMT)。本研究评估了丙磺舒(PROB)和对乙酰氨基酚(ACET)这两种也由UDP-葡糖醛酸基转移酶代谢的药物对大鼠肝细胞中AZT代谢和跨膜分布的影响。在加入10 μM [3H]AZT前30分钟将细胞预先暴露于350 μM PROB,可使细胞内GAZT水平降低约10倍。有趣的是,在PROB存在的情况下,AMT的形成增强了约1.5倍,这可能是由于AZT可用性增加所致。相反,在加入10 μM [3H]AZT前30分钟预先暴露于50 μM ACET,并未显著改变AZT的葡糖醛酸化。此外,PROB导致的AZT分解代谢减少对AZT的5'-磷酸化衍生物的形成没有贡献。因此,进行葡糖醛酸化的药物不一定会影响AZT向GAZT的转化,在与AZT联合给药之前,应使用体外系统研究它们的潜在相互作用。