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对MPTP去神经支配猴子进行慢性D1和D2多巴胺模拟物治疗:对基底神经节GABA(A)/苯二氮䓬受体复合物及GABA含量的影响

Chronic D1 and D2 dopaminomimetic treatment of MPTP-denervated monkeys: effects on basal ganglia GABA(A)/benzodiazepine receptor complex and GABA content.

作者信息

Calon F, Morissette M, Goulet M, Grondin R, Blanchet P J, Bédard P J, Di Paolo T

机构信息

Centre de Recherches en Endocrinologie Moléculaire, Le Centre Hospitalier Universitaire de Québec, Pavillon CHUL, Canada.

出版信息

Neurochem Int. 1999 Jul;35(1):81-91. doi: 10.1016/s0197-0186(99)00064-9.

Abstract

The effect of various chronic dopaminergic treatments in 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) monkeys on the brain gamma-aminobutyric acid type A (GABA(A)) /benzodiazepine receptor complex and GABA content was investigated in order to assess the GABAergic involvement in dopaminomimetic-induced dyskinesia. Three MPTP monkeys received for one month pulsatile administrations of the D1 dopamine (DA) receptor agonist SKF 82958 whereas three others received the same dose of SKF 82958 by continuous infusion. A long acting D2 DA receptor agonist, cabergoline, was given to another three animals. Untreated MPTP as well as naive control animals were also included. Pulsatile SKF 82958 relieved parkinsonian symptoms but was also associated with dyskinesia in two of the three animals whereas animals treated continuously with SKF 82958 remained as untreated MPTP monkeys. Chronic cabergoline administration improved motor response with no persistent dyskinesia. MPTP treatment induced a decrease of 3H-flunitrazepam binding in the medial anterior part of caudate-putamen and an increase in the internal segment of globus pallidus (GPi) which was in general unchanged by pulsatile or continuous SKF 82958 administration. Throughout the striatum, binding of 3H-flunitrazepam remained reduced in MPTP monkeys treated with cabergoline but was not significantly lower than untreated MPTP monkeys. Moreover, cabergoline treatment reversed the MPTP-induced increase in 3H-flunitrazepam binding in the GPi. GABA concentrations remained unchanged in the striatum, external segment of globus pallidus and GPi following MPTP denervation. Pulsatile but not continuous SKF 82958 administration decreased putamen GABA content whereas cabergoline treatment decreased caudate GABA. No alteration in GABA levels were observed in the GPe and GPi following the experimental treatments. These results suggest that: (1) D2-like receptor stimulation with cabergoline modulates GABA(A) receptor density in striatal subregions anatomically related to associative cortical afferent and (2) the absence of dyskinesia in dopaminomimetic-treated monkeys might be associated with the reversal of the MPTP-induced upregulation of the GABA(A)/benzodiazepine receptor complex in the Gpi.

摘要

为了评估γ-氨基丁酸能(GABAergic)系统在多巴胺模拟物诱发的运动障碍中的作用,研究了各种慢性多巴胺能治疗对1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)处理的猴子脑内γ-氨基丁酸A型(GABA(A))/苯二氮䓬受体复合物及GABA含量的影响。三只MPTP处理的猴子接受为期一个月的D1多巴胺(DA)受体激动剂SKF 82958的脉冲给药,而另外三只接受相同剂量SKF 82958的持续输注。给另外三只动物给予长效D2 DA受体激动剂卡麦角林。还纳入了未处理的MPTP猴子以及未处理的对照动物。脉冲式给予SKF 82958可缓解帕金森症状,但三只动物中有两只出现了运动障碍,而持续接受SKF 82958治疗的动物仍与未处理的MPTP猴子情况相同。长期给予卡麦角林可改善运动反应且无持续性运动障碍。MPTP处理导致尾状核-壳核内侧前部的3H-氟硝西泮结合减少,苍白球内侧段(GPi)增加,而脉冲式或持续给予SKF 82958对此一般无影响。在整个纹状体内,接受卡麦角林治疗的MPTP猴子的3H-氟硝西泮结合仍降低,但并不显著低于未处理的MPTP猴子。此外,卡麦角林治疗逆转了MPTP诱导的GPi中3H-氟硝西泮结合增加。MPTP去神经支配后,纹状体、苍白球外侧段和GPi中的GABA浓度保持不变。脉冲式而非持续给予SKF 82958可降低壳核GABA含量,而卡麦角林治疗可降低尾状核GABA含量。实验处理后,GPe和GPi中的GABA水平未观察到改变。这些结果表明:(1)用卡麦角林刺激D2样受体可调节与联合皮质传入相关的纹状体亚区的GABA(A)受体密度;(2)多巴胺模拟物处理的猴子中无运动障碍可能与MPTP诱导的Gpi中GABA(A)/苯二氮䓬受体复合物上调的逆转有关。

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