Pharmacological Manipulation of Cortical Inhibition in the Dorsolateral Prefrontal Cortex

被引:0
作者
Bahar Salavati
Tarek K Rajji
Reza Zomorrodi
Daniel M Blumberger
Robert Chen
Bruce G Pollock
Zafiris J Daskalakis
机构
[1] Centre for Addiction and Mental Health,Department of Psychiatry
[2] University of Toronto,Department of Psychiatry
[3] Campbell Family Mental Health Research Institute,Division of Neurology, Department of Medicine
[4] Centre for Addiction and Mental Health,undefined
[5] Temerty Centre for Therapeutic Brain Intervention,undefined
[6] Centre for Addiction and Mental Health,undefined
[7] University Health Network and University of Toronto,undefined
来源
Neuropsychopharmacology | 2018年 / 43卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Cortical inhibition (CI) occurs largely through GABA receptor-mediated inhibitory neurotransmission, which can be modulated by cholinergic, dopaminergic, and glutamatergic inputs. Transcranial magnetic stimulation (TMS) can be used to index CI through a paradigm known as long-interval CI (LICI). When TMS is combined with electroencephalography (EEG), LICI can index GABA receptor-mediated inhibitory neurotransmission in the dorsolateral prefrontal cortex (DLPFC). We conducted a hypothesis-driven pharmacological study to assess the role of cholinergic, dopaminergic, GABAergic, and glutamatergic neurotransmission on LICI from the DLPFC using TMS-EEG. In this randomized controlled, double-blind crossover within-subject study, 12 healthy participants received five sessions of LICI to the DLPFC in a random order, each preceded by the administration of placebo or one of the four active drugs. LICI was assessed after each drug administration and compared to LICI after placebo. Relative to placebo, baclofen resulted in a significant increase in LICI, while rivastigmine resulted in a significant decrease in LICI. Dextromethorphan and L-DOPA did not result in a significant change in LICI relative to placebo. Our study confirms that LICI in the DLPFC is largely mediated by GABAB receptor-mediated inhibitory neurotransmission and also suggests that cholinergic modulation decreases LICI in the DLPFC. Such findings may help guide future work examining the neurophysiological impact of these neurotransmitters in healthy and diseased states.
引用
收藏
页码:354 / 361
页数:7
相关论文
共 218 条
[1]  
Bestmann S(2015)The uses and interpretations of the motor-evoked potential for understanding behaviour Exp Brain Res 233 679-689
[2]  
Krakauer JW(2009)Impaired presynaptic inhibition in the motor cortex in Parkinson disease Neurology 72 842-849
[3]  
Chu J(1985)Differential effects of dextrorphan and levorphanol on the excitation of rat spinal neurons by amino acids Eur J Pharmacol 111 185-190
[4]  
Wagle-Shukla A(2014)Evidence for pretreatment LICI deficits among depressed children and adolescents with nonresponse to fluoxetine Brain Stimul 7 243-251
[5]  
Gunraj C(2008)Long-interval cortical inhibition from the dorsolateral prefrontal cortex: a TMS-EEG study Neuropsychopharmacology 33 2860-2869
[6]  
Lang AE(1972)The chemistry and kinetics of Lioresal Postgrad Med J 48 9-13
[7]  
Chen R(2010)Reliability of long-interval cortical inhibition in healthy human subjects: a TMS-EEG study J Neurophysiol 104 1339-1346
[8]  
Church J(1995)D1 and D2 receptor gene expression in the rat frontal cortex: cellular localization in different classes of efferent neurons Eur Neurosci 7 1050-1063
[9]  
Lodge D(2002)Mechanisms of dopamine activation of fast-spiking interneurons that exert inhibition in rat prefrontal cortex J Neurophysiol 88 3150-3166
[10]  
Berry SC(2010)Functional and dysfunctional synaptic plasticity in prefrontal cortex: roles in psychiatric disorders Biol Psychiatry 67 199-207