肌萎缩侧索硬化
兴奋毒性
嘌呤能受体
神经科学
疾病
医学
生物
受体
NMDA受体
病理
内科学
作者
André D. J. McKenzie,Taylor R. Garrett,Eryn L. Werry,Michael Kassiou
标识
DOI:10.1021/acschemneuro.2c00133
摘要
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease characterized by upper and lower motor neuron loss. The pathomechanisms of ALS are still poorly understood with current hypotheses involving genetic mutations, excitotoxicity, and reactive oxygen species formation. In the absence of a disease-altering clinically approved therapeutic, there is an ever-increasing need to identify new targets to develop drugs that delay disease onset and/or progression. The purinergic P2X7 receptor (P2X7R) has been implicated widely across the ALS realm, providing a potential therapeutic strategy. This review summarizes the current understanding of ALS, the P2X7R and its role in ALS, the current landscape of P2X7R antagonists, and the in vivo potential of these antagonists in preclinical ALS models.
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