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N-甲基-D-天冬氨酸对大鼠尾状核壳核切片中多巴胺释放的实时影响:一项使用快速循环伏安法的研究。

Real-time effects of N-methyl-D-aspartic acid on dopamine release in slices of rat caudate putamen: a study using fast cyclic voltammetry.

作者信息

Iravani M M, Kruk Z L

机构信息

Department of Pharmacology, Queen Mary and Westfield College, University of London, England.

出版信息

J Neurochem. 1996 Mar;66(3):1076-85. doi: 10.1046/j.1471-4159.1996.66031076.x.

Abstract

The functional role of N-methyl-D-aspartic acid (NMDA) glutamate receptors in the real-time regulation of single electrical pulse (1 p)-stimulated endogenous dopamine release was investigated in slices of rat caudate putamen using fast cyclic voltammetry at a carbon fibre electrode. In the presence of Mg2+, 20 microM NMDA had a weak effect on background signals but did not affect 1 p-stimulated dopamine release. Removal of Mg2+ increased the background and doubled 1 p-stimulated dopamine release. In the absence of Mg2+, 20 microM NMDA caused a transient "release" of dopamine and decreased the background signal. The 1 p-stimulated dopamine release was subsequently reduced. In the presence of 1 microM (+/-)-3-(2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP), superfusion with 20 microM NMDA did not cause a transient "release" of dopamine, and 1 p-stimulated dopamine release was not subsequently attenuated. In the presence of 1 microM tetrodotoxin, 1 p-stimulated dopamine release was abolished, but 20 microM NMDA still caused a transient "release" of dopamine. Removal of Ca2+ from the artificial CSF abolished 1 p-stimulated dopamine release and resulted in a decline in the baseline but did not affect dopamine "release" when 20 microM NMDA was added. The dopamine release-inducing effect of 20 microM NMDA was less pronounced in sites in the caudate putamen where dopamine release increased with frequency of electrical stimulation (hot spots) than in sites where there was little frequency-dependent dopamine release (cold spots). Subsequent 1 p-stimulated dopamine release was less attenuated in cold spots than in hot spots. We conclude that in the absence of Mg2+, NMDA induces release of dopamine by acting at CPP-sensitive NMDA receptors in a Ca(2+)-independent manner. This transient release depletes dopamine from a storage site from which dopamine is released by 1 p electrical stimulation. These real-time observations of the effects of NMDA on electrical stimulus-independent and -dependent dopamine release may explain the apparently conflicting observations of the effects of NMDA on dopamine release made in previous studies. They also indicate that dopamine release and storage are heterogeneous at different sites in the rat caudate putamen.

摘要

利用碳纤维电极上的快速循环伏安法,在大鼠尾状核壳核切片中研究了N-甲基-D-天冬氨酸(NMDA)谷氨酸受体在单电脉冲(1 p)刺激的内源性多巴胺释放实时调节中的功能作用。在存在Mg2+的情况下,20微摩尔NMDA对背景信号有微弱影响,但不影响1 p刺激的多巴胺释放。去除Mg2+会增加背景信号,并使1 p刺激的多巴胺释放量加倍。在不存在Mg2+的情况下,20微摩尔NMDA会导致多巴胺短暂“释放”,并降低背景信号。随后1 p刺激的多巴胺释放减少。在存在1微摩尔(±)-3-(2-羧基哌嗪-4-基)-丙基-1-膦酸(CPP)的情况下,用20微摩尔NMDA进行灌流不会引起多巴胺的短暂“释放”,随后1 p刺激的多巴胺释放也不会减弱。在存在1微摩尔河豚毒素的情况下,1 p刺激的多巴胺释放被消除,但20微摩尔NMDA仍会导致多巴胺短暂“释放”。从人工脑脊液中去除Ca2+会消除1 p刺激的多巴胺释放,并导致基线下降,但在添加20微摩尔NMDA时不影响多巴胺“释放”。在尾状核壳核中,多巴胺释放随电刺激频率增加的部位(热点),20微摩尔NMDA的多巴胺释放诱导作用不如多巴胺释放很少依赖频率的部位(冷点)明显。随后在冷点处1 p刺激的多巴胺释放减弱程度不如热点处。我们得出结论,在不存在Mg2+的情况下,NMDA通过以不依赖Ca2+的方式作用于对CPP敏感的NMDA受体来诱导多巴胺释放。这种短暂释放会使多巴胺从一个储存部位耗尽,而多巴胺通过1 p电刺激从该部位释放。这些关于NMDA对电刺激非依赖性和依赖性多巴胺释放影响的实时观察结果,可能解释了先前研究中关于NMDA对多巴胺释放影响的明显相互矛盾的观察结果。它们还表明,大鼠尾状核壳核不同部位的多巴胺释放和储存是异质性的。

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