首页> 美国卫生研究院文献>The Journal of Neuroscience >Locus ceruleus lesion by local 6-hydroxydopamine infusion causes marked and specific destruction of noradrenergic neurons long-term depletion of norepinephrine and the enzymes that synthesize it and enhanced dopaminergic mechanisms in the ipsilateral cerebral cortex
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Locus ceruleus lesion by local 6-hydroxydopamine infusion causes marked and specific destruction of noradrenergic neurons long-term depletion of norepinephrine and the enzymes that synthesize it and enhanced dopaminergic mechanisms in the ipsilateral cerebral cortex

机译:局部6-羟基多巴胺输注引起的蓝斑病灶会导致明显的和特定的去甲肾上腺素能神经元破坏去甲肾上腺素及其合成酶的长期消耗以及增强同侧大脑皮层的多巴胺能机制

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摘要

The local stereotaxic microinfusion of 5 micrograms of 6- hydroxydopamine in the region of the nucleus locus ceruleus causes severe loss of noradrenergic neurons with little evidence of nonspecific tissue reaction or destruction that could be detected by conventional light microscopic methods. Such lesion is accompanied by a marked and long-term depletion of norepinephrine and comparable loss of activity of its synthesizing enzymes, dopamine beta-hydroxylase and tyrosine hydroxylase, in the ipsilateral cerebral cortex. Locus ceruleus lesion was also found to increase tissue levels of dopamine and its metabolites, 3,4-dihydroxyphenylacetic acid and homovanillic acid, in the ipsilateral cortex. These results add further evidence to support the hypothesis that enhanced dopaminergic mechanisms may play a central role in compensating for chronic cortical noradrenergic denervation.
机译:在核蓝斑区域局部局部微滴5微克的6-羟基多巴胺会导致去甲肾上腺素能神经元的严重丧失,几乎没有非特异性组织反应或破坏的迹象,可以通过常规光学显微镜方法检测到。在同侧大脑皮层中,这种病变伴有去甲肾上腺素的明显和长期耗竭,其合成酶多巴胺β-羟化酶和酪氨酸羟化酶的活性也相应降低。蓝斑病灶病变也被发现增加同侧皮层中多巴胺及其代谢产物3,4-二羟基苯基乙酸和高香草酸的组织水平。这些结果提供了进一步的证据,以支持增强多巴胺能机制在补偿慢性皮质去甲肾上腺素能神经失调中起核心作用的假说。

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