nmda受体功能障碍破坏空间工作记忆的序列偏差

H. Stein, Joao Barbosa, J. Dalmau, A. Compte
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引用次数: 0

摘要

在工作记忆(WM)任务中,对先前项目的吸引力偏差是记忆持续时间整合的证据。这些连续偏差被建模为突触短期可塑性的产物,允许WM表征在突触痕迹中持续存在,即使神经活动恢复到基线值也会干扰下一次试验。我们假设NMDAR是短时增强(STP)和稳定WM延迟活动的关键组成部分,对视觉空间WM任务中的序列偏差至关重要。证实了这一假设,我们发现抗NMDAR脑炎和精神分裂症患者的偏倚大大减少,这两种疾病都与NMDAR功能减退有关。我们模拟了在持续延迟活动期间建立的Hebbian STP机制支持的尖峰神经网络中的序列偏差。我们发现,当STP水平逐渐降低时,患者和模型行为之间存在密切的对应关系,这表明精神分裂症和抗nmdar脑炎患者联合皮层的短期可塑性受到破坏。此外,我们还探讨了该模型在精神分裂症去抑制理论的基础上解释减少偏差的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NMDA-Receptor Dysfunction Disrupts Serial Biases in Spatial Working Memory
In working memory (WM) tasks, attractive biases to previous items are evidence for continuous temporal integration of memories. These serial biases have been modeled as a product of synaptic short-term plasticity, allowing WM representations to endure in a synaptic trace and interfere with the next trial even when neural activity returns to baseline values. We hypothesized that the NMDAR, a key component of both short-term potentiation (STP) and stable WM delay activity, would be of central importance to serial biases in a visuospatial WM task. Confirming this hypothesis, we found drastically reduced biases in patients with anti-NMDAR encephalitis and schizophrenia, both diseases that have been related to NMDAR hypofunction. We simulated serial biases in a spiking neural network supported by a Hebbian STP mechanism that builds up during persistent delay-activity. We found a close correspondence between patient and model behavior when gradually lowering levels of STP, suggesting a disruption of short-term plasticity in associative cortices of schizophrenic and anti-NMDAR encephalitis patients. Further, we explored the capability of the model to explain reduced biases in light of the disinhibition theory of schizophrenia.
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