神经科学
癫痫
生物
衰减
医学
心理学
物理
光学
作者
Naohisa Miyakawa,Yuji Nagai,Yukiko Hori,Koki Mimura,Asumi Orihara,Kei Oyama,Takeshi Matsuo,Ken‐ichi Inoue,Takafumi Suzuki,Toshiyuki Hirabayashi,Tetsuya Suhara,Masahiko Takada,Makoto Higuchi,Keisuke Kawasaki,Takafumi Minamimoto
标识
DOI:10.1038/s41467-023-36642-6
摘要
Abstract Epilepsy is a disorder in which abnormal neuronal hyperexcitation causes several types of seizures. Because pharmacological and surgical treatments occasionally interfere with normal brain function, a more focused and on-demand approach is desirable. Here we examined the efficacy of a chemogenetic tool—designer receptors exclusively activated by designer drugs (DREADDs)—for treating focal seizure in a nonhuman primate model. Acute infusion of the GABA A receptor antagonist bicuculline into the forelimb region of unilateral primary motor cortex caused paroxysmal discharges with twitching and stiffening of the contralateral arm, followed by recurrent cortical discharges with hemi- and whole-body clonic seizures in two male macaque monkeys. Expression of an inhibitory DREADD (hM4Di) throughout the seizure focus, and subsequent on-demand administration of a DREADD-selective agonist, rapidly suppressed the wide-spread seizures. These results demonstrate the efficacy of DREADDs for attenuating cortical seizure in a nonhuman primate model.
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