Fogel Maiah N, Khalil Alena, Khaled Sheikh F, Rodriguez Elizette M, Payne Keaton M, Blount Jesse R, Petschke Madison, Nizamuddin Roshan Ara, Jeidel Faige, Riven Vivienne, Petrosky Stephanie
Dr. Kiran C. Patel College of Osteopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL 33328, United States.
Nutr Rev. 2025 Jul 3. doi: 10.1093/nutrit/nuaf103.
The safety of aspartame, a widely consumed low-calorie artificial sweetener, for human consumption has recently been heavily debated. Published research has demonstrated that aspartame's breakdown products-aspartic acid, phenylalanine, and methanol-are associated with potential neurotoxicity and possible carcinogenic and metabolic effects in animal models. For this scoping review, existing literature on neurocognitive effects of aspartame was gathered and analyzed. A search of 3 literature databases (Embase, Ovid MEDLINE, and Web of Science) yielded 170 peer-reviewed, full-text articles. After consideration of exclusion criteria, 29 articles were selected for inclusion. After reviewing the findings, indications of aspartame's potential neurotoxic effects were demonstrated: multiple experimental studies revealed histopathological changes, such as elevated oxidative stress markers and neuronal loss, in various brain regions of animal models after exposure to aspartame. Additional studies showed memory and learning impairments in animal models, as well as behavioral dysfunction and mood disorders indicative of depression and anxiety in both animal and human models, illustrated by processes such as the downregulation of gamma aminobutyric acid signaling and upregulation of glutamate signaling in the amygdala. Notably, many of these studies investigated aspartame's impact not only at or above the Food and Drug Administration (FDA)-approved level, but below it as well. Two studies also indicated that populations with preexisting neurocognitive deficits, such as individuals with parkinsonism or preexisting metabolic conditions such as diabetes may have an increased vulnerability to neurocognitive harm when consuming aspartame. Interestingly, several agents were found to ameliorate aspartame's neurocognitive impacts, such as Pimpinella anisum oil and vitamin E. These negative neurocognitive effects and their potential mitigators demonstrate the necessity for further research into aspartame's possible impacts on health and safety at current FDA-approved levels, with additional consideration of certain populations at higher risk for neurocognitive injury.
阿斯巴甜是一种广泛食用的低热量人工甜味剂,其对人类食用的安全性最近受到了激烈辩论。已发表的研究表明,阿斯巴甜的分解产物——天冬氨酸、苯丙氨酸和甲醇——在动物模型中与潜在的神经毒性以及可能的致癌和代谢作用有关。为了进行这项范围综述,收集并分析了关于阿斯巴甜神经认知效应的现有文献。对3个文献数据库(Embase、Ovid MEDLINE和Web of Science)进行检索,得到了170篇经同行评审的全文文章。在考虑排除标准后,选择了29篇文章纳入。在审查研究结果后,证明了阿斯巴甜具有潜在神经毒性作用的迹象:多项实验研究显示,动物模型在接触阿斯巴甜后,其各个脑区出现了组织病理学变化,如氧化应激标志物升高和神经元丢失。其他研究表明,动物模型存在记忆和学习障碍,动物和人类模型中还存在行为功能障碍以及抑郁和焦虑等情绪障碍,杏仁核中γ-氨基丁酸信号下调和谷氨酸信号上调等过程说明了这一点。值得注意的是,许多这些研究不仅调查了阿斯巴甜在食品药品监督管理局(FDA)批准水平或以上的影响,也调查了其在批准水平以下的影响。两项研究还表明,患有帕金森病等先前存在神经认知缺陷的人群,或患有糖尿病等先前存在代谢疾病的人群,在食用阿斯巴甜时可能更容易受到神经认知损害。有趣的是,发现几种物质可以减轻阿斯巴甜的神经认知影响,如茴芹油和维生素E。这些负面的神经认知效应及其潜在的缓解剂表明,有必要进一步研究阿斯巴甜在FDA当前批准水平下对健康和安全可能产生的影响,并额外考虑某些神经认知损伤风险较高的人群。