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5-羟色胺能神经元介导帕金森病大鼠模型中 L-DOPA 诱导的多巴胺异常释放。

Serotonergic neurons mediate ectopic release of dopamine induced by L-DOPA in a rat model of Parkinson's disease.

机构信息

Université de Bordeaux, Unité Mixte de Recherche Centre National de la Recherche Scientifique 5227, Centre Hospitalier Universitaire de Bordeaux, 33076 Bordeaux cedex, France.

出版信息

Neurobiol Dis. 2010 Apr;38(1):136-43. doi: 10.1016/j.nbd.2010.01.012. Epub 2010 Jan 22.

Abstract

Benefit and motor side effects of l-DOPA in Parkinson's disease have been related to dopamine transmission in the striatum. However, the putative involvement of serotonergic neurons in the dopaminergic effects of l-DOPA suggests that the striatum is not a preferential target of l-DOPA. By using microdialysis in a rat model of Parkinson's disease, we found that l-DOPA (3-100 mg/kg) increased dopamine extracellular levels monitored simultaneously in four brain regions receiving serotonergic innervation: striatum, substantia nigra, hippocampus, prefrontal cortex. The increase was regionally similar at the lowest dose and 2-3 times stronger in the striatum at higher doses. Citalopram, a serotonin reuptake blocker, or the destruction of serotonergic fibers by 5,7-dihydroxytryptamine impaired l-DOPA-induced dopamine release in all regions. These data demonstrate that l-DOPA induces an ectopic release of dopamine due to serotonergic neurons. The new pattern of dopamine transmission created by l-DOPA may contribute to the benefit and side effects of l-DOPA.

摘要

左旋多巴在帕金森病中的益处和运动副作用与纹状体中的多巴胺传递有关。然而,5-羟色胺能神经元参与左旋多巴的多巴胺效应表明,纹状体不是左旋多巴的优先作用靶点。通过在帕金森病大鼠模型中使用微透析技术,我们发现左旋多巴(3-100mg/kg)增加了同时监测到的四个接受 5-羟色胺支配的脑区的多巴胺细胞外水平:纹状体、黑质、海马体和前额叶皮质。在最低剂量时,增加幅度在各区域相似,而在较高剂量时,在纹状体中的增加幅度则是 2-3 倍。西酞普兰,一种 5-羟色胺再摄取抑制剂,或 5,7-二羟基色胺破坏 5-羟色胺能纤维,均可损害所有区域的左旋多巴诱导的多巴胺释放。这些数据表明,左旋多巴诱导了由于 5-羟色胺能神经元导致的多巴胺异常释放。左旋多巴所产生的新的多巴胺传递模式可能有助于左旋多巴的益处和副作用。

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