神经科学
突触可塑性
神经毒性
自闭症
自闭症谱系障碍
认知
信号
脑源性神经营养因子
神经营养因子
加巴能
多巴胺能
精神分裂症(面向对象编程)
医学
生物
心理学
多巴胺能途径
变质塑性
长时程增强
神经传递
铅(地质)
钙信号传导
NMDA受体
不利影响
癫痫
神经可塑性
作者
Gouri Nair,Snigdha Adhikary,P Harshitha,Parithathvi Aluru,Herman Sunil Dsouza
标识
DOI:10.1080/09603123.2025.2612010
摘要
Lead is a toxic heavy metal that poses significant health risks, which include neurodevelopmental disorders such as autism spectrum disorder (ASD). This review examines the effects of lead neurotoxicity on synaptic pathways which are relatively unexplored and their potential role in the development of ASD. Lead exposure occurs through various environmental sources, including contaminated water, soil, paint, and industrial appliances. Once absorbed, lead accumulates in soft tissues and bones, causes prolonged neurological damage, especially in children. ASD is characterised by impaired communication, repetitive behaviours, and cognitive challenges, with increasing evidence linking environmental factors like heavy metal exposure to its onset. Synaptic signalling disruption is a key aspect of ASD and lead interferes with the synaptic pathways by inhibiting calcium influx, leading to cognitive impairments and memory issues. This review is an overview of the previously reported findings that explains the role of lead in reducing N-methyl-D-aspartate receptors (NMDAR) function, disrupting the brain-derived neurotrophic factor (BDNF) pathway, and impairing Wnt, GABAergic and dopaminergic signalling pathways. These alterations result in cognitive decline, impaired synaptic plasticity and increased ASD symptoms. Understanding these mechanisms is crucial for developing strategies to mitigate the adverse effects of lead exposure on neurodevelopment.
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