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首页> 外文期刊>Behavioural Brain Research: An International Journal >Dopaminergic responses in the core part of the nucleus accumbens to subcutaneous MK801 administration are increased following postnatal transient blockade of the prefrontal cortex
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Dopaminergic responses in the core part of the nucleus accumbens to subcutaneous MK801 administration are increased following postnatal transient blockade of the prefrontal cortex

机译:在前额叶皮层的后瞬时阻断后,核心核心核心核心核心的多巴胺能反应增加了前额叶皮层的后瞬态阻断

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摘要

Highlights ? Impact of postnatal inactivation of the prefrontal cortex on MK 801 reactivity. ? Increase of locomotor responses to MK 801 administration in adult rats. ? Increase of dopaminergic responses in the core subregion to MK 801 administration. ? Time courses of the increases in the two variables are close but not identical. ? Pathophysiology of schizophrenia: the involvement of the core warrants further study. Abstract Schizophrenia is a complex and devastating neuropsychiatric disease thought to result from impaired connectivity between several integrative regions, stemming from developmental failures. In particular, the left prefrontal cortex of schizophrenia patients seems to be targeted by such early developmental disturbances. Data obtained over the last three decades support the hypothesis of a dopaminergic dysfunction in schizophrenia. Striatal dopaminergic dysregulation in schizophrenia may result from a dysconnection between the prefrontal cortex and the striatum (dorsal and ventral) involving glutamatergic N -methyl- d -aspartate (NMDA) receptors. In the context of animal modeling of the pathophysiology of schizophrenia, the present study was designed to investigate the effects of MK 801 (dizocilpine) on locomotor activity and dopaminergic responses in the left core part of the nucleus accumbens (ventral striatum) in adult rats following neonatal tetrodotoxin inactivation of the left prefrontal cortex (infralimbic/prelimbic region) at postnatal day 8. Dopaminergic variations were recorded in the nucleus accumbens by means of in vivo voltammetry in freely moving adult animals. Following MK 801 administration, and in comparison to control (PBS) animals, animals microinjected with tetrodotoxin display locomotor hyperactivity and increased extracellular dopamine levels in the core part of the nucleus accumbens. These findings suggest neonatal functional inactivation of the prefrontal cortex may lead to a dysregulation of dopamine release in the core part of the nucleus accumbens involving NMDA receptors. The results obtained may provide new insight into the involvement of NMDA receptors in the pathophysiology of schizophrenia and suggest that future studies should look carefully at the core of the nucleus accumbens. ]]>
机译:强调 ?产后灭活前额叶皮层对MK 801反应性的影响。还成年大鼠MK 801给药的运动响应的增加。还核心子区域中的多巴胺能反应增加到MK 801给药。还两个变量增加的时间课程是关闭但不相同的。还精神分裂症的病理生理学:核心认股权证的参与进一步研究。摘要精神分裂症是一种复杂和毁灭性的神经精神病疾病,旨在引起几个综合区域之间的连通性受损,源于发育失败。特别是,精神分裂症患者的左前期皮质似乎是通过这种早期发育障碍的靶向。在过去三十年中获得的数据支持精神分裂症中多巴胺能功能障碍的假设。精神分裂症中的纹状体多巴胺能失衡可能是由涉及谷氨酰胺N-甲基-D-海岸酸盐(NMDA)受体的前额叶皮质和纹状体(背侧和腹侧)之间的脱节肌瘤。在精神分裂症病理学生理学的动物建模的背景下,本研究旨在探讨MK 801(Dizocilpine)对成年大鼠核心腺(腹侧纹状体)的左侧核心部分中的运动活性和多巴胺能反应的影响新生儿四曲毒素在后期8.在后期左前额叶皮质(Infralimbic / prelimbic区)的灭活8.通过在自由移动成人动物的体内伏安中,在细胞核中记录多巴胺能变化。在MK 801给药后,与对照(PBS)动物相比,动物微观注射了胞核毒素的核心部分核心部分的肺毒素展示过度活动和增加的细胞外多巴胺水平。这些发现表明前额叶皮质的新生儿功能失活可能导致涉及NMDA受体的细胞核核心的核心部分中的多巴胺释放的失调。获得的结果可以为NMDA受体在精神分裂症病理生理学中的累及中提供新的洞察力,并表明未来的研究应该在核心核心的核心上仔细观察。 ]]>

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