de la Monte Suzanne M, Goel Anuva, Tong Ming, Delikkaya Busra
Department of Pathology and Laboratory Medicine, Rhode Island Hospital, Lifespan Academic Institutions, and the Warren Alpert Medical School of Brown University, Providence, RI, USA.
Department of Medicine, Rhode Island Hospital, Lifespan Academic Institutions, and The Warren Alpert Medical School of Brown University, Providence, RI, USA.
J Alzheimers Dis Rep. 2023 Jul 20;7(1):751-766. doi: 10.3233/ADR-230046. eCollection 2023.
Agent Orange, an herbicide used during the Vietnam War, contains 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). Agent Orange has teratogenic and carcinogenic effects, and population-based studies suggest Agent Orange exposures lead to higher rates of toxic and degenerative pathologies in the peripheral and central nervous system (CNS).
This study examines the potential contribution of Agent Orange exposures to neurodegeneration.
Human CNS-derived neuroepithelial cells (PNET2) treated with 2,4-D and 2,4,5-T were evaluated for viability, mitochondrial function, and Alzheimer's disease (AD)-related proteins.
Treatment with 250μg/ml 2,4-D or 2,4,5-T significantly impaired mitochondrial function, caused degenerative morphological changes, and reduced viability in PNET2 cells. Correspondingly, glyceraldehyde-3-phosphate dehydrogenase expression which is insulin-regulated and marks the integrity of carbohydrate metabolism, was significantly inhibited while 4-hydroxy-2-nonenal, a marker of lipid peroxidation, was increased. Tau neuronal cytoskeletal protein was significantly reduced by 2,4,5-T, and relative tau phosphorylation was progressively elevated by 2,4,5-T followed by 2,4-D treatment relative to control. Amyloid-β protein precursor (AβPP) was increased by 2,4,5-T and 2,4-D, and 2,4,5-T caused a statistical trend (0.05 < p<0.10) increase in Aβ. Finally, altered cholinergic function due to 2,4,5-T and 2,4-D exposures was marked by significantly increased choline acetyltransferase and decreased acetylcholinesterase expression, corresponding with responses in early-stage AD.
Exposures to Agent Orange herbicidal chemicals rapidly damage CNS neurons, initiating a path toward AD-type neurodegeneration. Additional research is needed to understand the permanency of these neuropathologic processes and the added risks of developing AD in Agent Orange-exposed aging Vietnam Veterans.
橙剂是越战期间使用的一种除草剂,含有2,4-二氯苯氧乙酸(2,4-D)和2,4,5-三氯苯氧乙酸(2,4,5-T)。橙剂具有致畸和致癌作用,基于人群的研究表明,接触橙剂会导致外周和中枢神经系统(CNS)出现更高比例的毒性和退行性病变。
本研究探讨接触橙剂对神经退行性变的潜在影响。
对用2,4-D和2,4,5-T处理的人中枢神经系统来源的神经上皮细胞(PNET2)进行活力、线粒体功能和阿尔茨海默病(AD)相关蛋白的评估。
用250μg/ml的2,4-D或2,4,5-T处理显著损害线粒体功能,导致退行性形态变化,并降低PNET2细胞的活力。相应地,胰岛素调节的、标志着碳水化合物代谢完整性的甘油醛-3-磷酸脱氢酶表达显著受到抑制,而脂质过氧化标志物4-羟基-2-壬烯醛增加。2,4,5-T使tau神经元细胞骨架蛋白显著减少,相对于对照组,2,4,5-T处理后再用2,4-D处理,相对tau磷酸化逐渐升高。2,4,5-T和2,4-D使淀粉样β蛋白前体(AβPP)增加,2,4,5-T使Aβ有统计学趋势(0.05<p<0.10)增加。最后,2,4,5-T和2,4-D暴露导致的胆碱能功能改变表现为胆碱乙酰转移酶显著增加和乙酰胆碱酯酶表达减少,这与早期AD的反应一致。
接触橙剂中的除草化学物质会迅速损害中枢神经系统神经元,引发通往AD型神经退行性变的路径。需要进一步研究以了解这些神经病理过程的持久性以及接触橙剂的越南退伍军人在衰老过程中患AD的额外风险。