Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, 30912, Georgia.
Department of Pharmaceutical and Biomedical Sciences, The University of Georgia College of Pharmacy, 250 W. Green Street, Athens, 30602, Georgia.
Neurotoxicology. 2017 Sep;62:111-123. doi: 10.1016/j.neuro.2017.06.003. Epub 2017 Jun 12.
Chlorpyrifos (CPF) is an extensively used organophosphorus pesticide that has recently come under increasing scrutiny due to environmental health concerns particularly its association with neurodevelopmental defects. While the insecticidal actions and acute toxicity of CPF are attributed to its oxon metabolite (CPO) which potently inhibits the cholinergic enzyme acetylcholinesterase (AChE), there is significant evidence that CPF, CPO, and other organophosphates may affect a variety of neuronal targets and processes that are not directly related to AChE. Previously, in adult rat sciatic nerves ex vivo and postnatal neurons from rats in vitro we observed that CPF and CPO impaired the movements of vesicles and mitochondria in axons. Here, in embryonic neurons from rats in culture, we evaluated 24h exposures to CPF and CPO across picomolar to micromolar concentrations for effects on fast axonal transport of membrane bound organelles (MBOs) that contained the amyloid precursor protein (APP) tagged with the fluorescent marker, Dendra2 (APPDendra2). The most notable observations of this study were concentration-dependent decreases in the velocity and percentage of MBOs moving in the anterograde direction, an increase in the number of stationary MBOs, and an increased frequency of pauses associated with both CPF and CPO. These effects occurred at concentrations that did not significantly inhibit AChE activity, they were not blocked by cholinergic receptor antagonists, and they were not associated with compromised cell viability. These effects of CPF and CPO may be significant given the importance of axonal transport to neuronal development as well the function of fully developed neurons.
毒死蜱(CPF)是一种广泛使用的有机磷农药,由于对环境健康的关注,尤其是其与神经发育缺陷的关联,最近受到了越来越多的关注。虽然 CPF 的杀虫作用和急性毒性归因于其氧代代谢物(CPO),CPO 强烈抑制胆碱能酶乙酰胆碱酯酶(AChE),但有大量证据表明 CPF、CPO 和其他有机磷可能影响多种与 AChE 不直接相关的神经元靶标和过程。此前,我们在成年大鼠坐骨神经离体和体外培养的新生大鼠神经元中观察到 CPF 和 CPO 损害了轴突中囊泡和线粒体的运动。在这里,我们在培养的大鼠胚胎神经元中,评估了 CPF 和 CPO 在皮摩尔到微摩尔浓度范围内对含有荧光标记 Dendra2 的淀粉样前体蛋白(APP)标记的膜结合细胞器(MBOs)快速轴突运输的影响。这项研究最显著的观察结果是,MBOs 向顺行方向移动的速度和百分比呈浓度依赖性下降,静止 MBOs 的数量增加,与 CPF 和 CPO 相关的停顿频率增加。这些效应发生在 AChE 活性没有显著抑制的浓度下,它们不受胆碱能受体拮抗剂的阻断,也与细胞活力受损无关。鉴于轴突运输对神经元发育以及完全发育的神经元功能的重要性,CPF 和 CPO 的这些影响可能是重要的。