首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Orally administered atropine enhances motor cortex excitability: a transcranial magnetic stimulation study in human subjects.
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Orally administered atropine enhances motor cortex excitability: a transcranial magnetic stimulation study in human subjects.

机译:口服阿托品可增强运动皮层兴奋性:一项针对人类受试者的经颅磁刺激研究。

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摘要

Oral application of atropine was used to test if a modulation of cholinergic neurotransmission changed motor excitability. Healthy volunteers received either 1 or 2 mg atropine. Paired transcranial magnetic stimulation was used to study intracortical inhibition and intracortical facilitation before, 1 h and 24 h after ingestion of atropine. In addition, the silent period, motor threshold, F wave and motor response amplitudes were measured. The 1 mg dose of atropine induced a loss of intracortical inhibition, the 2 mg dose produced an intracortical disinhibition and enhanced intracortical facilitation. These changes returned to baseline after 24 h. Other electrophysiological parameters remained unchanged. Thus, an antagonist of pre- and postsynaptic muscarinic receptors increased excitability in the human motor cortex in a dose-dependent manner, indicating an influence of the cholinergic system on motor cortex excitation.
机译:口服阿托品用于测试胆碱能神经传递的调节是否改变了运动兴奋性。健康志愿者接受1或2毫克阿托品。配对经颅磁刺激用于研究阿托品摄入前,摄入后1 h和24 h的皮质内抑制和皮质内促进作用。此外,还测量了静默期,电机阈值,F波和电机响应幅度。 1 mg剂量的阿托品诱导皮质内抑制作用丧失,2 mg剂量产生皮质内抑制作用并增强皮质内促进作用。这些变化在24小时后恢复到基线。其他电生理参数保持不变。因此,突触前和突触后毒蕈碱受体的拮抗剂以剂量依赖性方式增加人运动皮层中的兴奋性,表明胆碱能系统对运动皮层兴奋的影响。

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