首页> 美国卫生研究院文献>Cerebral Cortex (New York NY) >Cortical Regulation of Striatal Medium Spiny Neuron Dendritic Remodeling in Parkinsonism: Modulation of Glutamate Release Reverses Dopamine Depletion–Induced Dendritic Spine Loss
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Cortical Regulation of Striatal Medium Spiny Neuron Dendritic Remodeling in Parkinsonism: Modulation of Glutamate Release Reverses Dopamine Depletion–Induced Dendritic Spine Loss

机译:帕金森病中纹状体中棘神经元树突重构的皮层调节:谷氨酸盐释放的调节逆转多巴胺消耗引起的树突棘损失。

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摘要

Striatal medium spiny neurons (MSNs) receive glutamatergic afferents from the cerebral cortex and dopaminergic inputs from the substantia nigra (SN). Striatal dopamine loss decreases the number of MSN dendritic spines. This loss of spines has been suggested to reflect the removal of tonic dopamine inhibitory control over corticostriatal glutamatergic drive, with increased glutamate release culminating in MSN spine loss. We tested this hypothesis in two ways. We first determined in vivo if decortication reverses or prevents dopamine depletion–induced spine loss by placing motor cortex lesions 4 weeks after, or at the time of, 6-hydroxydopamine lesions of the SN. Animals were sacrificed 4 weeks after cortical lesions. Motor cortex lesions significantly reversed the loss of MSN spines elicited by dopamine denervation; a similar effect was observed in the prevention experiment. We then determined if modulating glutamate release in organotypic cocultures prevented spine loss. Treatment of the cultures with the mGluR2/3 agonist to suppress corticostriatal glutamate release completely blocked spine loss in dopamine-denervated cultures. These studies provide the first evidence to show that MSN spine loss associated with parkinsonism can be reversed and point to suppression of corticostriatal glutamate release as a means of slowing progression in Parkinson's disease.
机译:纹状体中棘神经元(MSN)从大脑皮层接受谷氨酸能传入,从黑质(SN)接受多巴胺能输入。纹状体多巴胺损失减少了MSN树突棘的数量。有人认为这种脊柱丢失反映了对皮质皮质谷氨酸能驱动的强力多巴胺抑制性控制的去除,谷氨酸释放增加最终导致MSN脊柱丢失。我们以两种方式检验了这一假设。我们首先在体内通过将运动皮层病变置于SN的6-羟基多巴胺病变后4周或当时来确定脱皮是否逆转或阻止了多巴胺耗竭引起的脊柱丢失。皮质损伤4周后处死动物。运动皮层损伤明显逆转了由多巴胺去神经支配引起的MSN脊柱的丧失。在预防实验中观察到了相似的效果。然后,我们确定在器官型共培养物中调节谷氨酸释放是否可以防止脊柱丢失。用mGluR2 / 3激动剂对培养物进行处理以抑制皮质类固醇谷氨酸的释放,完全阻断了多巴胺去神经培养物中的脊柱丢失。这些研究提供了第一个证据,表明与帕金森氏症相关的MSN脊柱丢失可以逆转,并指出抑制皮质类固醇谷氨酸的释放是减缓帕金森氏病进展的一种手段。

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