Gullo Francesca, Ceriani Michela, D'Aloia Alessia, Wanke Enzo, Constanti Andrew, Costa Barbara, Lecchi Marzia
Department of Biotechnology and Biosciences and Milan Center for Neuroscience, University of Milano-BicoccaMilan, Italy.
Department of Biotechnology and Biosciences, University of Milano-BicoccaMilan, Italy.
Front Neurosci. 2017 Sep 6;11:500. doi: 10.3389/fnins.2017.00500. eCollection 2017.
Increasing evidence supports a decisive role for neuroinflammation in the neurodegenerative process of several central nervous system (CNS) disorders. Microglia are essential mediators of neuroinflammation and can regulate a broad spectrum of cellular responses by releasing reactive oxygen intermediates, nitric oxide, proteases, excitatory amino acids, and cytokines. We have recently shown that also in cortical networks of neurons, astrocytes and microglia, an increased level of tumor necrosis factor-alpha (TNF-α) was detected a few hours after exposure to the bacterial endotoxin lipopolysaccharide (LPS). Simultaneously, an atypical "seizure-like" neuronal network activity was recorded by multi-electrode array (MEA) electrophysiology. These effects were prevented by minocycline, an established anti-inflammatory antibiotic. We show here that the same inhibitory effect against LPS-induced neuroinflammation is exerted also by natural plant compounds, polyphenols, such as curcumin (CU, curcuma longa), crocin (CR, saffron), and resveratrol (RE, grape), as well as by the glucagon like peptide-1 receptor (GLP-1R) agonist exendin-4 (EX-4). The drugs tested also caused early transient (variable) changes of network activity. Since it has been reported that LPS-induced neuroinflammation causes rearrangements of glutamate transporters in astrocytes and microglia, we suggest that neural activity could be putatively increased by an imbalance of glial glutamate transporter activity, leading to prolonged synaptic glutamatergic dysregulation.
越来越多的证据支持神经炎症在几种中枢神经系统(CNS)疾病的神经退行性过程中起决定性作用。小胶质细胞是神经炎症的重要介质,可通过释放活性氧中间体、一氧化氮、蛋白酶、兴奋性氨基酸和细胞因子来调节广泛的细胞反应。我们最近发现,在神经元、星形胶质细胞和小胶质细胞的皮质网络中,暴露于细菌内毒素脂多糖(LPS)数小时后,肿瘤坏死因子-α(TNF-α)水平也会升高。同时,通过多电极阵列(MEA)电生理学记录到一种非典型的“癫痫样”神经元网络活动。这些作用可被米诺环素(一种已确立的抗炎抗生素)所阻止。我们在此表明,天然植物化合物多酚,如姜黄素(CU,姜黄)、藏红花素(CR,藏红花)和白藜芦醇(RE,葡萄),以及胰高血糖素样肽-1受体(GLP-1R)激动剂艾塞那肽-4(EX-4),对LPS诱导的神经炎症也具有相同的抑制作用。所测试的药物还引起了网络活动的早期短暂(可变)变化。由于据报道LPS诱导的神经炎症会导致星形胶质细胞和小胶质细胞中谷氨酸转运体的重排,我们推测神经活动可能因胶质谷氨酸转运体活性失衡而增加,从而导致突触谷氨酸能调节异常延长。