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In vitro neuronal network activity in NMDA receptor encephalitis
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 ter...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573950/ https://www.ncbi.nlm.nih.gov/pubmed/23379293 http://dx.doi.org/10.1186/1471-2202-14-17 |
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author | Jantzen, Sabine U Ferrea, Stefano Wach, Claudia Quasthoff, Kim Illes, Sebastian Scherfeld, Dag Hartung, Hans-Peter Seitz, Rüdiger J Dihné, Marcel |
author_facet | Jantzen, Sabine U Ferrea, Stefano Wach, Claudia Quasthoff, Kim Illes, Sebastian Scherfeld, Dag Hartung, Hans-Peter Seitz, Rüdiger J Dihné, Marcel |
author_sort | Jantzen, Sabine U |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3573950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35739502013-02-16 In vitro neuronal network activity in NMDA receptor encephalitis Jantzen, Sabine U Ferrea, Stefano Wach, Claudia Quasthoff, Kim Illes, Sebastian Scherfeld, Dag Hartung, Hans-Peter Seitz, Rüdiger J Dihné, Marcel BMC Neurosci Research Article 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. BioMed Central 2013-02-05 /pmc/articles/PMC3573950/ /pubmed/23379293 http://dx.doi.org/10.1186/1471-2202-14-17 Text en Copyright ©2013 Jantzen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Jantzen, Sabine U Ferrea, Stefano Wach, Claudia Quasthoff, Kim Illes, Sebastian Scherfeld, Dag Hartung, Hans-Peter Seitz, Rüdiger J Dihné, Marcel In vitro neuronal network activity in NMDA receptor encephalitis |
title | In vitro neuronal network activity in NMDA receptor encephalitis |
title_full | In vitro neuronal network activity in NMDA receptor encephalitis |
title_fullStr | In vitro neuronal network activity in NMDA receptor encephalitis |
title_full_unstemmed | In vitro neuronal network activity in NMDA receptor encephalitis |
title_short | In vitro neuronal network activity in NMDA receptor encephalitis |
title_sort | in vitro neuronal network activity in nmda receptor encephalitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573950/ https://www.ncbi.nlm.nih.gov/pubmed/23379293 http://dx.doi.org/10.1186/1471-2202-14-17 |
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