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血浆稳定性依赖性的酰基葡萄糖醛酸代谢物在人体内的循环:为何默沙东公司研发的米格列醇和礼来公司研发的吡格列酮的循环代谢产物谱可能导致风险评估产生误导。

Plasma stability-dependent circulation of acyl glucuronide metabolites in humans: how circulating metabolite profiles of muraglitazar and peliglitazar can lead to misleading risk assessment.

机构信息

Pharmaceutical Candidate Optimization, Bristol-Myers Squibb Research and Development, Princeton, New Jersey 08543, USA.

出版信息

Drug Metab Dispos. 2011 Jan;39(1):123-31. doi: 10.1124/dmd.110.035048. Epub 2010 Sep 28.

Abstract

Muraglitazar and peliglitazar, two structural analogs differing by a methyl group, are dual peroxisome proliferator-activated receptor-α/γ activators. Both compounds were extensively metabolized in humans through acyl glucuronidation to form 1-O-β-acyl glucuronide (AG) metabolites as the major drug-related components in bile, representing at least 15 to 16% of the dose after oral administration. Peliglitazar AG was the major circulating metabolite, whereas muraglitazar AG was a very minor circulating metabolite in humans. Peliglitazar AG circulated at lower concentrations in animal species than in humans. Both compounds had a similar glucuronidation rate in UDP-glucuronic acid-fortified human liver microsomal incubations and a similar metabolism rate in human hepatocytes. Muraglitazar AG and peliglitazar AG were chemically synthesized and found to be similarly oxidized through hydroxylation and O-demethylation in NADPH-fortified human liver microsomal incubations. Peliglitazar AG had a greater stability than muraglitazar AG in incubations in buffer, rat, or human plasma (pH 7.4). Incubations of muraglitazar AG or peliglitazar AG in plasma produced more aglycon than acyl migration products compared with incubations in the buffer. These data suggested that the difference in plasma stability, not differences in intrinsic formation, direct excretion, or further oxidation of muraglitazar AG or peliglitazar AG, contributed to the observed difference in the circulation of these AG metabolites in humans. The study demonstrated the difficulty in doing risk assessment based on metabolite exposure in plasma because the more reactive muraglitazar AG would not have triggered a threshold of concern based on the recent U.S. Food and Drug Administration guidance on Metabolites in Safety Testing, whereas the more stable peliglitazar AG would have.

摘要

马拉格列汀和吡格列汀是两种结构类似物,仅相差一个甲基,它们都是双重过氧化物酶体增殖物激活受体-α/γ激动剂。这两种化合物在人体内均通过酰基葡萄糖醛酸化广泛代谢,形成 1-O-β-酰基葡萄糖醛酸(AG)代谢物,是胆汁中主要的与药物相关的成分,代表口服给药后至少 15%至 16%的剂量。吡格列汀 AG 是主要的循环代谢物,而马拉格列汀 AG 是人体内非常次要的循环代谢物。吡格列汀 AG 在动物体内的循环浓度低于人体内的浓度。这两种化合物在 UDP-葡萄糖醛酸强化的人肝微粒体孵育中具有相似的葡萄糖醛酸化速率,在人肝细胞中的代谢速率也相似。马拉格列汀 AG 和吡格列汀 AG 均通过化学合成得到,并在 NADPH 强化的人肝微粒体孵育中发现通过羟化和 O-去甲基化而被相似地氧化。吡格列汀 AG 在缓冲液、大鼠或人血浆(pH7.4)孵育中的稳定性大于马拉格列汀 AG。与缓冲液孵育相比,在血浆中孵育马拉格列汀 AG 或吡格列汀 AG 产生的糖苷元比酰基迁移产物更多。这些数据表明,导致这些 AG 代谢物在人体内循环差异的原因是血浆稳定性的差异,而不是内在形成、直接排泄或马拉格列汀 AG 或吡格列汀 AG 的进一步氧化的差异。该研究表明,基于血浆中代谢物暴露进行风险评估存在困难,因为更具反应性的马拉格列汀 AG 不会根据美国食品和药物管理局最近关于安全测试中代谢物的指南引发关注阈值,而更稳定的吡格列汀 AG 则会。

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