Mou Si, Hummer B Timothy, Yuan Jiaqi, Huang Yue, Liang Meina, Faggioni Raffaella, Roskos Lorin K, Rosenbaum Anton I
Integrated Bioanalysis, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, South San Francisco, California 94080, United States.
Cardiovascular, Renal and Metabolism Safety, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Gaithersburg, Maryland 20878, United States.
ACS Pharmacol Transl Sci. 2025 Apr 4;8(5):1282-1291. doi: 10.1021/acsptsci.4c00563. eCollection 2025 May 9.
During nonclinical development of an oral formulation for a glucagon-like peptide-1 (GLP-1) receptor agonist, MEDI7219, toxicology studies revealed that propyl gallate (PG), when administered in enteric-coated (EC) tablets, led to nephrotoxicity in beagles. While PG has been widely used in food and cosmetics as an antioxidant, understanding of its toxicology, metabolism, and pharmacokinetics has been rarely discussed. To elucidate the nephrotoxicity observed after administration of PG in an EC tablet formulation, we employed dog and human renal proximal tubule epithelial cells (RPTECs). We observed greater cytotoxicity to PG in dog RPTECs compared to human cells and greater increases in response to PG treatment of glutathione in human cells compared to dog cells. Glutathione elevation is a common response to detoxify xenobiotics, especially ones that produce free radicals such as PG. We hypothesize that glutathione in human RPTECs was elevated to detoxify PG, but not in dog RPTECs, leading to greater cytotoxicity for dog RPTECs. However, a subsequent study in dogs demonstrated that the oral administration of PG in a non-EC capsule did not result in renal toxicity, suggesting the physiological response to PG is modulated by the mode of absorption and a blunted glutathione response may not completely explain the PG-related renal toxicity observed in dogs. Furthermore, to characterize the pharmacokinetics and metabolism of PG we developed a 10-plex, highly sensitive and robust LC-MS/MS-based quantification method for PG and its phase-I and phase-II metabolites. The methods were employed to support preclinical dog studies and clinical study (NCT03362593).
在胰高血糖素样肽-1(GLP-1)受体激动剂MEDI7219口服制剂的非临床开发过程中,毒理学研究表明,当以肠溶包衣(EC)片剂形式给药时,没食子酸丙酯(PG)会导致比格犬出现肾毒性。虽然PG作为抗氧化剂已广泛应用于食品和化妆品中,但对其毒理学、代谢和药代动力学的了解却鲜有讨论。为了阐明在EC片剂制剂中给药PG后观察到的肾毒性,我们使用了犬和人肾近端小管上皮细胞(RPTECs)。我们观察到,与人类细胞相比,PG对犬RPTECs的细胞毒性更大;与犬细胞相比,人类细胞对PG处理谷胱甘肽的反应增加幅度更大。谷胱甘肽升高是对外源化学物解毒的常见反应,尤其是对产生自由基的物质如PG。我们推测,人RPTECs中的谷胱甘肽升高是为了对PG进行解毒,但犬RPTECs中并非如此,这导致犬RPTECs的细胞毒性更大。然而,随后在犬身上进行的一项研究表明,以非EC胶囊形式口服PG不会导致肾毒性,这表明对PG的生理反应受吸收方式调节,而谷胱甘肽反应减弱可能无法完全解释在犬身上观察到的与PG相关的肾毒性。此外,为了表征PG的药代动力学和代谢,我们开发了一种基于10重、高灵敏度且稳健的液相色谱-串联质谱(LC-MS/MS)的PG及其I相和II相代谢物定量方法。这些方法被用于支持临床前犬类研究和临床研究(NCT03362593)。