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有证据表明,全身给药的多巴胺拮抗剂主要通过阻断树突体自身受体来激活多巴胺神经元放电。

Evidence that systemically administered dopamine antagonists activate dopamine neuron firing primarily by blockade of somatodendritic autoreceptors.

作者信息

Pucak M L, Grace A A

机构信息

Department of Neuroscience, University of Pittsburgh, Pennsylvania.

出版信息

J Pharmacol Exp Ther. 1994 Dec;271(3):1181-92.

PMID:7996424
Abstract

Systemic administration of dopamine antagonists increases the activity of some dopamine neurons in the substantia nigra, and this effect is thought to occur through two potential mechanisms: 1) local blockade of dopamine acting at somatodendritic autoreceptors or 2) blockade of receptors on postsynaptic targets in the striatum, resulting in long-loop feedback modulation. Several studies have provided evidence that the major influence is via striatonigral feedback. In this study, we tested the latter model by comparing the actions of systemically administered dopamine antagonists on dopamine neuron activation after removing striatonigral feedback. Systemic administration of either haloperidol or of the dopamine D2-specific antagonist sulpiride caused significant increases in the firing rate of many dopamine neurons recorded both in intact rats and in rats with hemisection of the striatonigral projection. Dopamine cells recorded in hemisected rats did not show consistent differences in either the proportion of cells excited or in the magnitude of the excitation produced by antagonist administration. The magnitude of dopamine cell excitation occurring with antagonist administration was dependent on the spontaneous firing rate of the recorded cell, with slow-firing neurons generally exhibiting the largest excitatory responses. These results provide evidence that blockade of dopamine neurons in the striatum is not the primary mechanism by which systemically administered dopamine antagonists excite dopamine neurons. Thus, dopamine antagonists most likely increase dopamine cell firing rate by blockade of somatodendritic autoreceptors, suggesting that the basal activity of the cells is dependent in part on dendritically released dopamine within the substantia nigra.

摘要

多巴胺拮抗剂的全身给药会增加黑质中一些多巴胺神经元的活性,这种效应被认为通过两种潜在机制发生:1)作用于树突体自身受体的多巴胺的局部阻断,或2)纹状体中突触后靶点上受体的阻断,导致长环反馈调节。多项研究已提供证据表明主要影响是通过纹状体黑质反馈。在本研究中,我们通过比较在去除纹状体黑质反馈后全身给药的多巴胺拮抗剂对多巴胺神经元激活的作用,来测试后一种模型。氟哌啶醇或多巴胺D2特异性拮抗剂舒必利的全身给药,在完整大鼠和纹状体黑质投射半切的大鼠中记录的许多多巴胺神经元的放电率均显著增加。在半切大鼠中记录的多巴胺细胞,在被拮抗剂给药激发的细胞比例或激发幅度方面均未显示出一致的差异。拮抗剂给药时发生的多巴胺细胞兴奋幅度取决于所记录细胞的自发放电率,通常放电慢的神经元表现出最大的兴奋反应。这些结果提供了证据,表明纹状体中多巴胺神经元的阻断不是全身给药的多巴胺拮抗剂兴奋多巴胺神经元的主要机制。因此,多巴胺拮抗剂很可能通过阻断树突体自身受体来增加多巴胺细胞的放电率,这表明细胞的基础活性部分依赖于黑质内从树突释放的多巴胺。

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