Rossi Silvia, Studer Valeria, Motta Caterina, De Chiara Valentina, Barbieri Francesca, Bernardi Giorgio, Centonze Diego
Clinica Neurologica, Dipartimento di Neuroscienze, Università Tor Vergata, Rome, Italy.
Mult Scler. 2012 Nov;18(11):1633-5. doi: 10.1177/1352458512440207. Epub 2012 Mar 14.
Abnormal glutamate-dependent synaptic excitation contributes to neuronal damage in multiple sclerosis (MS). Little is known about the involvement of the GABA system in this disorder. Here we found that cerebrospinal fluid (CSF) from MS patients with enhanced brain lesions on magnetic resonance imaging inhibited GABA transmission in mouse brain slices. Enhanced IL-1β neuronal action was responsible for this effect, because IL-1β receptor antagonist blocked, and exogenous IL-1β mimicked the synaptic effect of inflamed CSF. Our results provide evidence that focal inflammation in MS perturbs the cytokine milieu within the circulating CSF, resulting in diffuse GABAergic alteration in neurons.
异常的谷氨酸依赖性突触兴奋会导致多发性硬化症(MS)中的神经元损伤。关于γ-氨基丁酸(GABA)系统在这种疾病中的作用知之甚少。在这里,我们发现,磁共振成像显示脑损伤增强的MS患者的脑脊液(CSF)会抑制小鼠脑片上的GABA传递。IL-1β神经元作用增强是造成这种效应的原因,因为IL-1β受体拮抗剂可阻断这种作用,而外源性IL-1β可模拟炎症脑脊液的突触效应。我们的结果提供了证据,表明MS中的局灶性炎症会扰乱循环脑脊液中的细胞因子环境,导致神经元中弥漫性GABA能改变。