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Cholinergic receptor alterations in the cerebral cortex of spinal cord injured rat

机译:脊髓损伤大鼠大脑皮质胆碱能受体的改变

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Many areas of the cerebral cortex process sensory information or coordinate motor output necessary for control of movement. Disturbances in cortical cholinergic system can affect locomotor coordination. Spinal cord injury causes severe motor impairment and disturbances in cholinergic signalling can aggravate the situation. Considering the impact of cortical cholinergic firing in locomotion, we focussed the study in understanding the cholinergic alterations in cerebral cortex during spinal cord injury. The gene expression of key enzymes in cholinergic pathway - acetylcholine esterase and choline acetyl transferase showed significant upregulation in the cerebral cortex of spinal cord injured group compared to control with the fold increase in expression of acetylcholine esterase prominently higher than cholineacetyl transferase. The decreased muscarinic receptor density and reduced immunostaining of muscarinic receptor subtypes along with down regulated gene expression of muscarinic M1 and M3 receptor subtypes accounts for dysfunction of metabotropic acetylcholine receptors in spinal cord injury group. Ionotropic acetylcholine receptor alterations were evident from the decreased gene expression of alpha 7 nicotinic receptors and reduced immunostaining of alpha 7 nicotinic receptors in confocal imaging. Our data pin points the disturbances in cortical cholinergic function due to spinal cord injury; which can augment the locomotor deficits. This can be taken into account while devising a proper therapeutic approach to manage spinal cord injury. Highlights ? Spinal cord injury (SCI) can affect cortical cholinergic signalling. ? Diminished activity of motor cortex can augment the injury severity. ? Muscarinic and nicotinc acetyl choline receptors were decreased in SCI. ? Disturbed expression of enzymes in cholinergic metabolism was also observed. ? Proper regulation of cholinergic system can be targeted for management of SCI.
机译:大脑皮层的许多区域处理感觉信息或协调运动控制所需的运动输出。皮质胆碱能系统的紊乱可影响运动协调。脊髓损伤会导致严重的运动障碍,胆碱能信号传导障碍会加剧这种情况。考虑到皮质胆碱能放电对运动的影响,我们将研究重点放在了解脊髓损伤期间大脑皮质的胆碱能改变。胆碱能途径中关键酶的基因表达-乙酰胆碱酯酶和胆碱乙酰基转移酶在脊髓损伤组的大脑皮层中显示出明显的上调,​​而对照组中乙酰胆碱酯酶的表达增加倍数明显高于胆碱乙酰基转移酶。毒蕈碱受体密度的降低和毒蕈碱受体亚型的免疫染色降低以及毒蕈碱M1和M3受体亚型的基因表达下调是脊髓损伤组代谢型乙酰胆碱受体功能障碍的原因。从共焦成像中α7烟碱样受体的基因表达降低和α7烟碱样受体的免疫染色降低可以明显看出离子型乙酰胆碱受体的改变。我们的数据针指出了脊髓损伤引起的皮质胆碱能功能障碍。这会增加运动功能障碍。在设计适当的治疗方法来管理脊髓损伤时可以考虑到这一点。强调 ?脊髓损伤(SCI)可能会影响皮质胆碱能信号传导。 ?运动皮层活动减少可增加损伤的严重程度。 ?毒蕈碱和烟碱乙酰胆碱受体在脊髓损伤中减少。 ?还观察到胆碱能代谢中酶的表达受干扰。 ?适当调节胆碱能系统可以作为SCI的治疗目标。

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