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A loss of hippocampal perineuronal nets produces deficits in dopamine system function: relevance to the positive symptoms of schizophrenia

机译:海马神经周围神经网络的丧失导致多巴胺系统功能的缺陷:与精神分裂症的阳性症状有关

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摘要

Deficits in parvalbumin containing interneurons are a consistent observation in animal models and schizophrenia patients. These neurons are surrounded by chondroitin sulfate proteoglycans, forming perineuronal nets, thought to support the high firing frequencies observed in these neurons. A loss of perineuronal nets has been observed post mortem in human schizophrenia patients, however, whether this contributes to the symptoms of schizophrenia is not known. Here we directly examine the effects of chondroitinase ABC degradation of ventral hippocampal (vHipp) perineuronal nets, and demonstrate that this results in an enhanced hippocampal activity and significant increase in dopamine neuron population activity. In addition, chondroitinase-treated rats display an augmented locomotor response to amphetamine, consistent with the enhanced response to psychomotor stimulants observed in schizophrenia patients. Taken together, these data demonstrate that a loss of vHipp perineuronal nets is sufficient, in and of itself, to induce aberrant hippocampal and dopamine system function consistent with that observed in rodent models and schizophrenia patients.
机译:在动物模型和精神分裂症患者中,一致的观察到含有小白蛋白的中间神经元缺乏。这些神经元被硫酸软骨素蛋白多糖包围,形成神经周围神经网,被认为可以支持在这些神经元中观察到的高放电频率。在人类精神分裂症患者中验尸后观察到神经周围神经网的丢失,但是,这是否有助于精神分裂症的症状尚不清楚。在这里,我们直接检查软骨素酶ABC降解腹侧海马(vHipp)神经周围神经网络的影响,并证明这导致海马活动增强和多巴胺神经元种群活动显着增加。另外,用软骨素酶处理的大鼠对苯丙胺的运动反应增强,这与在精神分裂症患者中观察到的对精神运动兴奋剂的反应增强有关。综上所述,这些数据表明,vHipp神经周围神经网的丧失本身足以诱发异常的海马和多巴胺系统功能,这与在啮齿动物模型和精神分裂症患者中观察到的一致。

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