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体外 NMDA 受体脑炎中的神经元网络活动。

In vitro neuronal network activity in NMDA receptor encephalitis.

机构信息

Department of Neurology, LVR-Klinikum Duesseldorf, Bergische Landstrasse 2, 40629, Duesseldorf, Germany.

出版信息

BMC Neurosci. 2013 Feb 5;14:17. doi: 10.1186/1471-2202-14-17.

DOI:10.1186/1471-2202-14-17
PMID:23379293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3573950/
Abstract

BACKGROUND

Anti-NMDA-encephalitis is caused by antibodies against the N-methyl-D-aspartate receptor (NMDAR) and characterized by a severe encephalopathy with psychosis, epileptic seizures and autonomic disturbances. It predominantly occurs in young women and is associated in 59% with an ovarian teratoma.

RESULTS

We describe effects of cerebrospinal fluid (CSF) from an anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis patient on in vitro neuronal network activity (ivNNA). In vitro NNA of dissociated primary rat cortical populations was recorded by the microelectrode array (MEA) system.The 23-year old patient was severely affected but showed an excellent recovery following multimodal immunomodulatory therapy and removal of an ovarian teratoma. Patient CSF (pCSF) taken during the initial weeks after disease onset suppressed global spike- and burst rates of ivNNA in contrast to pCSF sampled after clinical recovery and decrease of NMDAR antibody titers. The synchrony of pCSF-affected ivNNA remained unaltered during the course of the disease.

CONCLUSION

Patient CSF directly suppresses global activity of neuronal networks recorded by the MEA system. In contrast, pCSF did not regulate the synchrony of ivNNA suggesting that NMDAR antibodies selectively regulate distinct parameters of ivNNA while sparing their functional connectivity. Thus, assessing ivNNA could represent a new technique to evaluate functional consequences of autoimmune encephalitis-related CSF changes.

摘要

背景

抗 N-甲基-D-天冬氨酸受体(NMDAR)脑炎是由针对 NMDAR 的抗体引起的,其特征为伴有精神病、癫痫发作和自主神经紊乱的严重脑病。它主要发生在年轻女性中,59%与卵巢畸胎瘤有关。

结果

我们描述了抗 N-甲基-D-天冬氨酸受体(NMDAR)脑炎患者的脑脊液(CSF)对体外神经元网络活动(ivNNA)的影响。通过微电极阵列(MEA)系统记录分离的原代大鼠皮质群体的体外 NNA。该 23 岁患者病情严重,但经多模式免疫调节治疗和切除卵巢畸胎瘤后,恢复良好。与临床恢复和 NMDAR 抗体滴度下降后采集的 pCSF 相比,疾病发作初期采集的患者 CSF(pCSF)可显著抑制体外 NNA 的全局尖峰和爆发率。在疾病过程中,受 pCSF 影响的 ivNNA 的同步性保持不变。

结论

患者 CSF 直接抑制 MEA 系统记录的神经元网络的整体活性。相比之下,pCSF 并未调节 ivNNA 的同步性,这表明 NMDAR 抗体选择性地调节体外 NNA 的不同参数,而不会影响其功能连接。因此,评估体外 NNA 可能代表一种评估与自身免疫性脑炎相关 CSF 变化的功能后果的新技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d4a/3573950/ab78d1b950b2/1471-2202-14-17-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d4a/3573950/d5aabb05bb6f/1471-2202-14-17-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d4a/3573950/9c850758b62d/1471-2202-14-17-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d4a/3573950/ab78d1b950b2/1471-2202-14-17-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d4a/3573950/d5aabb05bb6f/1471-2202-14-17-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d4a/3573950/9c850758b62d/1471-2202-14-17-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d4a/3573950/ab78d1b950b2/1471-2202-14-17-3.jpg

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