阿尔茨海默病患者的尖峰时间依赖皮质-皮质可塑性受损。
Impaired Spike Timing Dependent Cortico-Cortical Plasticity in Alzheimer's Disease Patients.
机构信息
Department of Behavioural and Clinical Neurology, Non-invasive Brain Stimulation Unit, Santa Lucia Foundation IRCCS, Rome, Italy.
Department of System Medicine, Tor Vergata University, Rome, Italy.
出版信息
J Alzheimers Dis. 2018;66(3):983-991. doi: 10.3233/JAD-180503.
BACKGROUND
Mechanisms of cortical plasticity have been recently investigated in Alzheimer's disease (AD) patients with transcranial magnetic stimulation protocols showing a clear impairment of long-term potentiation (LTP) cortical-like plasticity mechanisms.
OBJECTIVE
We aimed to investigate mechanisms of cortico-cortical spike-timing dependent plasticity (STDP) in AD patients investigating the connections between posterior parietal cortex (PPC) and primary motor cortex (M1).
METHODS
We used a cortico-cortical paired associative stimulation (cc-PAS) protocol to repeatedly activate the connection between PPC and M1 of the left-dominant hemisphere in a sample of fifteen AD patients and ten age-matched healthy subjects. PPC transcranial magnetic stimulation preceded (ccPAS +5) or followed M1 stimulation (ccPAS - 5) by 5 ms. Motor-evoked potentials (MEPs) were collected to assess the time course of the after effects of cc-PAS protocol measuring MEP amplitude as index of cortico-cortical associative plasticity.
RESULTS
In healthy subjects, ccPAS - 5 protocol induced the expected long-lasting increase of MEP amplitude compatible with LTP-like cortical plasticity while PAS +5 protocol induced the opposite effect. AD patients did not show any significant modification of the amplitude of MEP after both ccPAS protocols.
CONCLUSIONS
Our study shows that in AD patients the time-locked activation of human cortico-cortical connections is not able to form STDP, reflecting an impairment of a multi-factor plasticity process.
背景
最近利用经颅磁刺激方案研究了阿尔茨海默病(AD)患者的皮质可塑性机制,这些方案显示长时程增强(LTP)皮质样可塑性机制明显受损。
目的
我们旨在研究 AD 患者皮质-皮质尖峰时间依赖可塑性(STDP)的机制,调查顶叶后皮质(PPC)和初级运动皮质(M1)之间的连接。
方法
我们使用皮质-皮质成对关联刺激(cc-PAS)方案,在 15 名 AD 患者和 10 名年龄匹配的健康受试者的左侧优势半球的 PPC 和 M1 之间反复激活连接。PPC 经颅磁刺激在前(ccPAS +5)或在 M1 刺激后(ccPAS - 5)5 ms 进行。采集运动诱发电位(MEPs)以评估 cc-PAS 方案的后效时间过程,测量 MEP 幅度作为皮质-皮质关联可塑性的指标。
结果
在健康受试者中,ccPAS - 5 方案诱导了预期的长时间增强 MEP 幅度,与 LTP 样皮质可塑性兼容,而 PAS +5 方案则诱导了相反的效果。AD 患者在两种 ccPAS 方案后均未显示 MEP 幅度的任何显著变化。
结论
我们的研究表明,在 AD 患者中,人类皮质-皮质连接的定时激活不能形成 STDP,反映出多因素可塑性过程受损。