Neuroscience Graduate Program, University of Virginia, Charlottesville, Virginia, USA.
Department of Neurology, University of Virginia, Charlottesville, Virginia, USA.
Epilepsia. 2021 Sep;62(9):e147-e152. doi: 10.1111/epi.17004. Epub 2021 Jul 31.
Dopamine type 2 receptor (D2R) agonists have anticonvulsant effect, whereas D2R antagonists increase seizure risk, but the mechanism of this action has not been delineated. We tested whether D2R agonists activate parvalbumin (PV)-containing inhibitory interneurons to suppress seizures. We treated frontal lobe onset seizures with a D2R agonist sumanirole, and it suppressed seizures. We used activity reporter TRAP2 mice and found that injection of D2R agonist led to extensive activation of PV interneurons in the cortex and striatum ipsilateral to the seizure focus. D2R agonists activate PV interneurons, which in turn inhibit principal neurons, potentially explaining their anticonvulsant effect.
多巴胺 2 型受体 (D2R) 激动剂具有抗惊厥作用,而 D2R 拮抗剂则增加癫痫发作的风险,但这种作用的机制尚未阐明。我们测试了 D2R 激动剂是否通过激活含有钙结合蛋白 parvalbumin (PV) 的抑制性中间神经元来抑制癫痫发作。我们用 D2R 激动剂 sumanirole 治疗额叶起始性癫痫发作,发现它可以抑制癫痫发作。我们使用活动报告基因 TRAP2 小鼠,发现 D2R 激动剂注射会导致癫痫灶同侧皮层和纹状体中 PV 中间神经元的广泛激活。D2R 激动剂激活 PV 中间神经元,进而抑制主神经元,这可能解释了它们的抗惊厥作用。