Ortiz Darlene Mae D, Hoang Ngoc Minh-Hong, Lee Handule, Park Juyoung, Park Kwangsik
College of Pharmacy, Dongduk Women's University, 60, Hwarang-ro, 13-gil, Seongbuk-gu, Seoul, 02748 Republic of Korea.
Toxicol Res. 2025 May 6;41(4):407-415. doi: 10.1007/s43188-025-00292-1. eCollection 2025 Jul.
4-Methylbenzophenone (4-MBP), a derivative of benzophenone commonly utilized in consumer products, has elicited significant safety concerns due to its potential to migrate from food packaging materials and its structural similarity to known toxicants. This investigation sought to elucidate the toxicological profile of 4-MBP in female Sprague-Dawley rats following a 7-day repeated oral exposure to doses of 100, 200, and 400 mg/kg. The results demonstrated pronounced toxicity, as evidenced by high mortality, decreased body weight, clinical signs of weakness, and increased relative liver weights. Biochemical analysis revealed significant elevations in liver enzymes (AST, ALT, and GGT), lipid dysregulation, and increased glucose levels, which are indicative of hepatic dysfunction. Histopathological examination confirmed hepatocyte hypertrophy and mild renal tubular vacuolation, suggesting hepatotoxicity and nephrotoxicity, respectively. Hematological findings further revealed a decrease in white blood cell counts and alterations in immune cell populations, indicating a compromised immune function. Notably, no significant pulmonary lesions were observed, suggesting organ-specific toxicity. This study provides critical insights into the toxic effects of 4-MBP, identifies hepatotoxic and nephrotoxic risks, and highlights the need for further investigation in the field of regulatory toxicology. The present findings are crucial for determining safe exposure limits and contributing to the regulatory assessment of 4-MBP safety and public health risks.
4-甲基二苯甲酮(4-MBP)是二苯甲酮的一种衍生物,常用于消费品中,由于其有可能从食品包装材料中迁移出来,且其结构与已知有毒物质相似,已引起了人们对其安全性的重大关注。本研究旨在阐明雌性Sprague-Dawley大鼠在连续7天口服100、200和400毫克/千克剂量的4-MBP后的毒理学特征。结果显示出明显的毒性,表现为高死亡率、体重减轻、虚弱的临床症状以及相对肝脏重量增加。生化分析显示肝酶(AST、ALT和GGT)显著升高、脂质代谢失调以及血糖水平升高,这些均表明肝功能障碍。组织病理学检查证实肝细胞肥大和轻度肾小管空泡化,分别提示肝毒性和肾毒性。血液学检查结果进一步显示白细胞计数减少以及免疫细胞群体发生变化,表明免疫功能受损。值得注意的是,未观察到明显的肺部病变,提示存在器官特异性毒性。本研究为4-MBP的毒性作用提供了关键见解,确定了肝毒性和肾毒性风险,并强调了在监管毒理学领域进行进一步研究的必要性。目前的研究结果对于确定安全暴露限值以及促进对4-MBP安全性和公共健康风险的监管评估至关重要。