近日,華南師范大學環境學院應光國教授、趙建亮研究員團隊2021級碩士研究生張源源等人在《Environment Pollution》上發表了題為“In vitro metabolism of the emerging contaminant 6PPD-quinone in human and rat liver microsomes: Kinetics, pathways, and mechanism”的論文(DOI: 10.1016/j.envpol.2024.123514,IF=8.9)。該研究使用IPHASE肝微粒體產品以體外代謝反應體系探究了輪胎添加劑的抗氧化劑6PPD及其轉化產物6PPD醌(6PPD-Q)的I相代謝情況,通過疑似篩查和非靶向的分析方法闡明了可能的轉化產物及轉化路徑,結合表型分析實驗與分子對接明確了代謝6PPD-Q的關鍵作用酶。
發表于《Science》上論文之前報道了6PPD-Q對銀鮭魚的急性致死效應,引起了世界范圍的廣泛關注,輪胎添加劑的安全性備受質疑。6PPD-Q是橡膠抗氧化劑6PPD經臭氧氧化的轉化產物,廣泛存在于各種環境介質中,可通過吸入、食入和皮膚接觸等多種途徑進入人體,進而進一步進入人體的代謝系統。本研究以肝微粒體體外孵育體系探究6PPD和6PPD-Q的生物轉化情況,探討6PPD-Q對人體健康可能的影響。
此項研究結果表明研究6PPD-Q 在較低濃度下代謝顯著,但在高濃度下代謝程度降低。關鍵I 相代謝產物為單加氧和進一步氧化的產物。與6PPD相比,6PPD-Q所需的代謝時間相對較長,代謝40 μg/L 6PPD的半衰期(t1/2)為28.9 min,而代謝16 μg/L 6PPD-Q的 t1/2則需要29.6 min,代謝80 μg/L 6PPD-Q的 t1/2則要達到254 min。這也說明與輪胎添加劑母體相比,轉化產物更難被人體所代謝,可能帶來更大的環境健康問題。未來的研究應重點關注輪胎添加劑轉化產物,特別是其他PPD-Qs的轉化產物,以充分評估其對人類健康的影響。
摘 要
N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine-quinone (6PPD-Q) is an ozonation product of the rubber antioxidant N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD). 6PPD-Q has recently been detected in various environmental media, which may enter the human body via inhalation and skin contact pathways. However, the human metabolism of 6PPD-Q has remained unknown. This study investigated the in vitro Cytochrome P450-mediated metabolism of 6PPD-Q in human and rat liver microsomes (HLMs and RLMs). 6PPD-Q was significantly metabolized at lower concentrations but slowed at high concentrations. The intrinsic clearance (CLint) of 6PPD-Q was 21.10 and 18.58 μL min− 1 mg− 1 protein of HLMs and RLMs, respectively, suggesting low metabolic ability compared with other reported pollutants. Seven metabolites and one intermediate were identified, and metabolites were predicted immunotoxic or mutagenic toxicity. Mono- and di-oxygenation reactions were the main phase I in vitro metabolic pathways. Enzyme inhibition experiments and molecular docking techniques were further used to reveal the metabolic mechanism. CYP1A2, 3A4, and 2C19, especially
CYP1A2, play critical roles in 6PPD-Q metabolism in HLMs, whereas 6PPD-Q is extensively metabolized in RLMs. Our study is the first to demonstrate the in vitro metabolic profile of 6PPD-Q in HLMs and RLMs. The results will significantly contribute to future human health management targeting the emerging pollutant 6PPD-Q.
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