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多巴胺再摄取的抑制:对黑质多巴胺能神经元活动的意义。

Inhibition of dopamine re-uptake: significance for nigral dopamine neuron activity.

作者信息

Engberg G, Elverfors A, Jonason J, Nissbrandt H

机构信息

Karolinska Institute, Department of Physiology and Pharmacology, Stockholm, Sweden.

出版信息

Synapse. 1997 Feb;25(2):215-26. doi: 10.1002/(SICI)1098-2396(199702)25:2<215::AID-SYN12>3.0.CO;2-X.

Abstract

In the present study the effect of inhibition of the re-uptake of dopamine (DA) was analysed with respect to DA release and to the firing pattern of DA neurons in the substantia nigra (SN). Intravenous administration of GBR 12909 (0.5-8 mg/kg), a specific and potent inhibitor of DA re-uptake, was found to dose-dependently increase the DA concentration both in the SN and in the striatum, as measured by microdialysis. However, the drug failed to significantly affect the firing rate of the nigral DA neurons. In contrast, GBR 12909 dose-dependently induced a regularisation of the firing pattern, concomitant with a reduction in burst activity. An acute hemisection of the brain, which by itself produced a slight regularisation of the firing pattern of the nigral DA neurons without changing the firing rate of the ability of the DA neurons to fire in bursts, was found to prevent the regulatory action of GBR 12909. Pretreatment with the selective GABAB-receptor antagonist CGP 35348 (200 mg/kg, i.v., 5 min) did not significantly affect the firing rate, the regularity of the DA neurons, or their ability to fire in bursts. However, CGP 35348 markedly antagonised the ability of GBR 12909 to induce pacemaker-like firing or a decrease in burst activity of the nigral DA neurons. The results of the present study suggest that a striatonigral feedback projection may serve to control the activity of nigral DA neurons not primarily by regulating the firing rate, but, preferably, by modulating the firing pattern of the neurons. In this regard, activation of somatodendritic GABAB-receptors may form the final link in this feedback inhibitory control system.

摘要

在本研究中,针对多巴胺(DA)再摄取的抑制作用,分析了其对DA释放以及黑质(SN)中DA神经元放电模式的影响。通过微透析测定发现,静脉注射GBR 12909(0.5 - 8 mg/kg),一种特异性且强效的DA再摄取抑制剂,会剂量依赖性地增加SN和纹状体中的DA浓度。然而,该药物未能显著影响黑质DA神经元的放电频率。相反,GBR 12909剂量依赖性地诱导放电模式规则化,同时爆发活动减少。发现大脑急性半横切本身会使黑质DA神经元的放电模式略有规则化,而不改变DA神经元爆发放电的频率或能力,且能阻止GBR 12909的调节作用。用选择性GABAB受体拮抗剂CGP 35348(200 mg/kg,静脉注射,5分钟)预处理,对DA神经元的放电频率、放电规则性或其爆发放电能力没有显著影响。然而,CGP 35348显著拮抗了GBR 12909诱导黑质DA神经元产生起搏器样放电或减少爆发活动的能力。本研究结果表明,纹状体 - 黑质反馈投射可能主要不是通过调节放电频率,而是通过调节神经元的放电模式来控制黑质DA神经元的活动。在这方面,树突 - 胞体GABAB受体的激活可能构成这种反馈抑制控制系统的最终环节。

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