Fondazione Santa Lucia IRCCS, Rome, Italy.
J Alzheimers Dis. 2012;31(3):593-9. doi: 10.3233/JAD-2012-120532.
In animal models of Alzheimer's disease (AD), amyloid-β fragments interfere with mechanisms of cortical plasticity such as long-term potentiation (LTP) and long-term depression (LTD). In the current study, we applied repetitive transcranial magnetic stimulation over the primary motor cortex (M1) in AD patients and in age-matched healthy controls, using protocols of theta burst stimulation (TBS) that are known to induce plastic changes resembling the LTP and LTD mechanisms described in animal models. AD patients showed consistent LTD-like effects that were comparable to those obtained in healthy controls when submitted to 40 seconds of continuous TBS. Conversely, AD patients did not show any LTP-like after effect when submitted to two different TBS protocols that induced an LTP-like effect in healthy controls such as intermittent TBS and 20 seconds of continuous TBS followed by one minute of muscular contraction. These results demonstrate the impairment of LTP-like together with normal LTD-like cortical plasticity in AD patients.
在阿尔茨海默病(AD)的动物模型中,淀粉样β片段干扰皮质可塑性的机制,如长时程增强(LTP)和长时程抑制(LTD)。在本研究中,我们在 AD 患者和年龄匹配的健康对照组中应用经颅重复磁刺激(rTMS)于初级运动皮层(M1),使用已知诱导类似于动物模型中描述的 LTP 和 LTD 机制的可塑性变化的 theta 爆发刺激(TBS)方案。当 AD 患者接受 40 秒连续 TBS 时,他们表现出一致的 LTD 样效应,与健康对照组获得的效应相当。相反,当 AD 患者接受两种不同的 TBS 方案时,他们没有表现出任何 LTP 样后效,这两种方案在健康对照组中诱导出 LTP 样效应,如间歇性 TBS 和 20 秒连续 TBS 后 1 分钟肌肉收缩。这些结果表明 AD 患者的 LTP 样和正常 LTD 样皮质可塑性受损。