Zou Zhiyang Zack, Han Ming-Jie, Chang Yu, Li Guiying
Department of DMPK & TOX, Global Health Drug Discovery Institute, Zhongguancun Dongsheng International Science Park, Beijing 100192, China.
TB Alliance, 80 Pine St. 20th Floor, New York, NY 10005, USA.
Molecules. 2024 Dec 4;29(23):5724. doi: 10.3390/molecules29235724.
AE90015 is a highly specific and effective negative allosteric modulator (NAM) for the human mGlu5 receptor, showing significant promise for treating Parkinson's disease. An in vivo rat oral dose study was conducted on AE90015, which involved the collection of urine and bile samples over a 24 h period. At the study's endpoint, plasma, liver, brain, and renal tissues were also collected. A total of 30 metabolites of AE90015 were identified and structurally characterized or detected using high-resolution LC-MS/MSn. These metabolites fall into four categories: mono-hydroxyl, di-hydroxyl, mono-hydroxyl glucuronide, and di-hydroxyl glucuronide. This study provided a comprehensive overview of the metabolism, excretion, and disposition of AE90015, a promising NAM. The primary clearance pathway for AE90015 is mono-oxidation, accounting for 96% of the total, while direct excretion via renal and bile routes accounted for only 0.5%. Bile emerged as the predominant excretion route, at 65%, for metabolites and a minor amount of parent compound, which contrasts with the common assumption that urine would be the primary excretion pathway, which accounted for 26%. Each adamantyl and pyrazine moiety of AE90015 undergoes a one-time oxidation, while the pyridyl portion remains unmetabolized. Secondary metabolites, such as di-hydroxylated forms and glucuronide conjugates, do not contribute to clearance. In this work, a new quantification method combining UV and mass spectra integration was developed, allowing for the quantification of overlapping metabolite peaks. This novel approach proved to be highly effective for metabolite identification in early preclinical studies.
AE90015是一种针对人代谢型谷氨酸受体5(mGlu5)的高度特异性且有效的负变构调节剂(NAM),在治疗帕金森病方面显示出巨大潜力。对AE90015进行了一项大鼠体内口服剂量研究,该研究涉及在24小时内收集尿液和胆汁样本。在研究终点,还收集了血浆、肝脏、大脑和肾脏组织。使用高分辨率液相色谱-串联质谱(LC-MS/MSn)共鉴定并对30种AE90015的代谢产物进行了结构表征或检测。这些代谢产物分为四类:单羟基、二羟基、单羟基葡萄糖醛酸苷和二羟基葡萄糖醛酸苷。本研究全面概述了有前景的NAM——AE90015的代谢、排泄和处置情况。AE90015的主要清除途径是单氧化,占总量的96%,而通过肾脏和胆汁途径的直接排泄仅占0.5%。胆汁成为代谢产物和少量母体化合物的主要排泄途径,占65%,这与通常认为尿液是主要排泄途径(占26%)的假设形成对比。AE90015的每个金刚烷基和吡嗪部分都经历一次氧化,而吡啶部分未发生代谢。二羟基化形式和葡萄糖醛酸苷缀合物等次要代谢产物对清除没有贡献。在这项工作中,开发了一种结合紫外光谱和质谱积分的新定量方法,可对重叠的代谢产物峰进行定量。这种新方法在临床前早期研究中被证明对代谢产物鉴定非常有效。