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小鼠黑质中多巴胺功能调控引起的运动变化的生化关联

Biochemical correlates of motor changes caused by the manipulation of dopamine function in the substantia nigra of the mouse.

作者信息

Bradbury A J, Costall B, Kelly M E, Naylor R J, Smith J A

出版信息

Neuropharmacology. 1985 Dec;24(12):1155-61. doi: 10.1016/0028-3908(85)90148-0.

Abstract

2-Di-n-propylamino-5,6-dihydroxytetralin, injected bilaterally into the substantia nigra of the mouse, caused dose-dependent motor inhibition which was associated with decreased levels of DOPAC and increased levels of dopamine in the striatum. (-)Sulpiride, injected into the substantia nigra, antagonised the locomotor depression although the partial antagonism of the elevation in the level of dopamine in the striatum and of the reduction in levels of DOPAC did not achieve significance. The specificity of the action of tetralin on dopamine receptors was shown by the failure of prazosin and yohimbine to antagonise the locomotor depression induced by tetralin and the reduction in levels of DOPAC. The selectivity of the action of tetralin for the dopamine system was shown by its failure to affect levels of noradrenaline, serotonin and 5-hydroxyindoleacetic acid in the striatum. The injection of tetralin into the substantia nigra also caused biochemical changes in limbic areas (nucleus accumbens and tuberculum olfactorium), where the levels of dopamine and DOPAC were elevated, and in the frontal cortex where the levels of DOPAC were reduced. These changes were antagonised by a concomitant injection of (-)sulpiride into the substantia nigra. It is concluded that the action of dopamine agonists in the midbrain can decrease the functional activity in the ascending dopaminergic pathways.

摘要

双侧注射2 - 二正丙基氨基 - 5,6 - 二羟基四氢萘到小鼠黑质,会引起剂量依赖性运动抑制,这与纹状体中3,4 - 二羟基苯乙酸(DOPAC)水平降低及多巴胺水平升高有关。向黑质注射(-)舒必利可拮抗运动抑制,尽管对纹状体中多巴胺水平升高及DOPAC水平降低的部分拮抗作用未达到显著水平。哌唑嗪和育亨宾未能拮抗四氢萘诱导的运动抑制及DOPAC水平降低,这表明四氢萘作用于多巴胺受体具有特异性。四氢萘对纹状体中去甲肾上腺素、5 - 羟色胺及5 - 羟吲哚乙酸水平无影响,表明其对多巴胺系统作用具有选择性。向黑质注射四氢萘还会引起边缘区域(伏隔核和嗅结节)的生化变化,其中多巴胺和DOPAC水平升高,以及额叶皮质中DOPAC水平降低。同时向黑质注射(-)舒必利可拮抗这些变化。结论是,多巴胺激动剂在中脑的作用可降低多巴胺能上行通路的功能活性。

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