Retired from a career in regulatory toxicology and risk assessment.
Birth Defects Res. 2020 Apr 1;112(6):445-479. doi: 10.1002/bdr2.1661. Epub 2020 Mar 1.
Exposure to chlorpyrifos (CPF), a neurotoxic insecticide, is implicated with adverse neurodevelopmental effects in children through noncholinergic mechanisms.
This review presents qualitative and quantitative evidence in three animal models (rodent, zebrafish, and Caenorhabditis elegans), for neurodevelopmental and behavioral effects occurring at CPF doses lower than those inhibiting acetylcholinesterase (AChE).
CPF treatment in rodents at low noncholinergic doses during neurodevelopment showed behavioral effects, including locomotor activity, neuromotor function (NMF), cognition, anxiety, social behavior, and maternal care. Zebrafish and C. elegans, which are transparent during development, allow for detailed analysis of specific systems; further, they exhibit neurotoxic effects closely emulating those observed in mammalian pathways. Qualitative results showed concordance among rodents, zebrafish and C. elegans for adverse effects on locomotor activity, NMF, and AChE inhibition. Male rodents had greater sensitivity for effects on locomotor activity than females and exposure during the gestation day 10-14 window showed consistent increases in locomotor activity at low CPF doses (≤1.0 mg kg day ). Zebrafish had cognitive and anxiety deficits after CPF treatment at low doses and young adult C. elegans had reproductive dysfunction associated NMF and disruption of the serotonergic pathway. Quantitative data for all three species showed neurobehavioral effects after exposure to CPF doses approximately 2-10-fold below the threshold for AChE inhibition.
Taken together, these findings provided a weight-of-evidence for low-dose CPF neurotoxicity and noncholinergic mechanisms. Variability in laboratories, exposure methods, tests, sex, and animal species/strain might have contributed to the inconsistent results. The detrimental CPF effects during early development are relevant to human populations.
接触毒死蜱(CPF)这种神经毒性杀虫剂,通过非胆碱能机制,与儿童不良神经发育效应有关。
本综述通过三种动物模型(啮齿动物、斑马鱼和秀丽隐杆线虫),呈现了在低于抑制乙酰胆碱酯酶(AChE)剂量下发生的神经发育和行为效应的定性和定量证据。
在神经发育过程中,用低非胆碱能剂量的 CPF 处理啮齿动物,显示出行为效应,包括运动活性、神经运动功能(NMF)、认知、焦虑、社会行为和母性行为。斑马鱼和秀丽隐杆线虫在发育过程中是透明的,允许对特定系统进行详细分析;此外,它们表现出的神经毒性效应与在哺乳动物途径中观察到的非常相似。定性结果表明,在啮齿动物、斑马鱼和秀丽隐杆线虫中,对运动活性、NMF 和 AChE 抑制的不良影响具有一致性。雄性啮齿动物对运动活性的影响比雌性更为敏感,在妊娠第 10-14 天暴露于 CPF 时,在低 CPF 剂量(≤1.0mg·kg-1·天-1)下运动活性持续增加。斑马鱼在低剂量 CPF 处理后出现认知和焦虑缺陷,而年轻成年秀丽隐杆线虫的 NMF 出现生殖功能障碍,并破坏了 5-羟色胺能途径。所有三种物种的定量数据都显示,在接触大约 2-10 倍低于 AChE 抑制阈值的 CPF 剂量后,出现神经行为效应。
总的来说,这些研究结果为低剂量 CPF 的神经毒性和非胆碱能机制提供了有力的证据。实验室、暴露方法、测试、性别和动物物种/品系的变异性可能导致了结果的不一致。早期发育期间 CPF 的有害影响与人类群体有关。