Baroni Anna, Moulton Chantalle, Cristina Mario, Sansone Luigi, Belli Manuel, Tasciotti Ennio
Human Longevity Program, IRCCS San Raffaele Roma, 00166 Rome, Italy.
Laboratory of Molecular, Cellular and Ultrastructural Pathology, IRCCS San Raffaele Roma, 00166 Rome, Italy.
Nanomaterials (Basel). 2025 Sep 4;15(17):1361. doi: 10.3390/nano15171361.
Nano- and microplastics (NMPs), with nanoplastics posing higher risks due to their smaller size and greater capacity for cellular and subcellular penetration, are being referred to as ubiquitous environmental neurotoxicants, due to their ability to pass through biological barriers, including the blood-brain barrier (BBB) and nasal olfactory epithelium, and to remain lodged in neural tissue. Upon uptake, such particles disturb neuronal homeostasis by multiple converging pathways, including oxidative stress, mitochondrial dysfunction, pathological protein aggregation, and chronic neuroinflammation, all closely involved with the molecular signatures of neurodegenerative disorders (Alzheimer's, Parkinson's, Amyotrophic Lateral Sclerosis-ALS). In addition to their neurotoxicity, recent findings suggest that NMPs could disturb synaptic communication and neuroplasticity, thereby compromising the brain's capacity to recover from an injury, a trauma, or neurodegeneration, thus impacting the progression of the disease, our ability to treat it and eventually the efficacy of rehabilitation approaches. Despite these findings, our understanding remains hampered by analytical issues, the scarcity of standard detection methods, and a total lack of longitudinal studies in humans. This review combines multidisciplinary evidence on brain-plastic interactions and calls for accelerated advances in our ability to monitor bioaccumulation in humans, and to integrate neurotoxicology paradigms in the assessment of this underappreciated but growing threat to brain health.
纳米塑料和微塑料(NMPs),其中纳米塑料因其更小的尺寸和更强的细胞及亚细胞穿透能力而具有更高的风险,由于它们能够穿过包括血脑屏障(BBB)和鼻嗅觉上皮在内的生物屏障,并滞留在神经组织中,正被视为无处不在的环境神经毒素。一旦被摄取,这些颗粒会通过多种汇聚途径扰乱神经元内环境稳态,包括氧化应激、线粒体功能障碍、病理性蛋白质聚集和慢性神经炎症,所有这些都与神经退行性疾病(阿尔茨海默病、帕金森病、肌萎缩侧索硬化症 - ALS)的分子特征密切相关。除了它们的神经毒性外,最近的研究结果表明,NMPs可能会扰乱突触通讯和神经可塑性,从而损害大脑从损伤、创伤或神经退行性变中恢复的能力,进而影响疾病的进展、我们治疗疾病的能力以及最终康复方法的疗效。尽管有这些发现,但我们的理解仍然受到分析问题、标准检测方法的匮乏以及完全缺乏人体纵向研究的阻碍。本综述结合了关于脑可塑性相互作用的多学科证据,并呼吁加快提高我们监测人体生物蓄积的能力,并将神经毒理学范式纳入对这一未得到充分认识但日益增长的脑健康威胁的评估中。