Oregon Institute of Occupational Health Sciences and Department of Neurology, School of Medicine, Oregon Health & Science University, Portland, OR, USA.
Toxicol Pathol. 2020 Apr;48(3):411-421. doi: 10.1177/0192623320910960. Epub 2020 Mar 12.
Peripheral neuropathy associated with chronic occupational and deliberate overexposure to neurotoxic organic solvents results from axonal degeneration in the central and peripheral nervous system. Human and experimental studies show that axonopathy is triggered by the action of neuroprotein-reactive γ-diketone metabolites formed from exposure to certain aliphatic solvents (-hexane, 2-hexanone) and aromatic compounds (1,2-diethylbenzene, 1,2-4-triethylbenzene, 6-acetyl-1,1,4,4-tetramethyl-7-ethyl-1,2,3,4-tetralin). Neuroprotein susceptibility is related primarily to their differential content of lysine, the ∊-amino group of which is targeted by γ-diketones. Specific neuroprotein targets have been identified, and the sequence of molecular mechanisms leading to axonal pathology has been illuminated. While occupational -hexane neuropathy continues to be reported, lessons learned from its experimental study may have relevance to other causes of peripheral neuropathy, including those associated with aging and diabetes mellitus.
与慢性职业性和故意过度暴露于神经毒性有机溶剂相关的周围神经病,源自中枢和周围神经系统的轴突变性。人体和实验研究表明,轴突病是由暴露于某些脂肪族溶剂(正己烷、2-己酮)和芳香族化合物(1,2-二乙基苯、1,2,4-三乙基苯、6-乙酰基-1,1,4,4-四甲基-7-乙基-1,2,3,4-四氢萘)形成的神经蛋白反应性γ-二酮代谢物的作用引发的。神经蛋白易感性主要与其赖氨酸含量有关,赖氨酸的ε-氨基是γ-二酮的靶标。已经确定了特定的神经蛋白靶标,并阐明了导致轴突病理学的分子机制序列。虽然职业性正己烷神经病仍有报道,但从其实验研究中获得的经验教训可能与其他周围神经病的病因有关,包括与衰老和糖尿病相关的病因。