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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >L-DOPA elicits non-vesicular releases of serotonin and dopamine in hemiparkinsonian rats in vivo
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L-DOPA elicits non-vesicular releases of serotonin and dopamine in hemiparkinsonian rats in vivo

机译:L-DOPA在体内诱发半帕金森氏病大鼠中非水泡素和多巴胺的释放

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摘要

The control of the secretory activity of serotonergic neurons has been pointed out to reduce motor and non-motor side effects of the antiparkinsonian drug L-DOPA. This strategy deserves further investigation because it is presently unclear whether L-DOPA promotes a non-vesicular release of dopamine and serotonin from serotonergic neurons. To get a full neurochemical picture compatible with the existence of such a mechanism, we combined multisite intracerebral microdialysis, post mortem tissue measurement and single unit extracellular recordings in the dorsal raphe nucleus from hemiparkinsonian rats. L-DOPA (3-100 mg/kg, ip.) non-homogeneously decreased extracellular serotonin levels in the striatum, substantia nigra pars reticulata, hippocampus and prefrontal cortex and homogenously serotonin tissue content in the striatum, cortex and cerebellum. L-DOPA (12 mg/kg) did not modify the firing rate or pattern of serotonergic-like neurons recorded in the dorsal raphe nucleus. When focusing on serotonin release in the prefrontal cortex and the hippocampus, we found that L-DOPA (12 or 100 mg/kg) enhanced serotonin extracellular levels in both regions upon Cat removal. Concomitantly, L-DOPA-stimulated dopamine release partly persisted in the absence of Ca2+ in a region-dependent manner. Local application of the serotonin reuptake inhibitor citalopram (1 mu M) blunted the responses to L-DOPA (3-12 mg/kg), measured as extracellular dopamine levels, most prominently in the hippocampus. These data stress that L-DOPA, already at low to moderate doses, promotes non-vesicular releases of serotonin and dopamine in a region dependent manner. (C) 2016 Elsevier B.V. and ECNP. All rights reserved.
机译:已经指出,控制5-羟色胺能神经元的分泌活性可以减少抗帕金森病药物L-DOPA的运动和非运动副作用。该策略值得进一步研究,因为目前尚不清楚L-DOPA是否会促进5-羟色胺从5-羟色胺能神经元的非囊泡释放。为了获得与这种机制的存在兼容的完整神经化学图谱,我们将多部位脑内微透析,验尸组织测量和半帕金森氏症大鼠背核中的单单位细胞外记录相结合。 L-DOPA(3-100 mg / kg,ip。)非均匀地降低纹状体,黑质,网状海马,海马和前额叶皮层中的细胞外血清素水平,并均匀地降低纹状体,皮质和小脑中的血清素组织含量。 L-DOPA(12 mg / kg)不会改变背ra核中记录的血清素样神经元的放电速率或模式。当着眼于额叶前额叶皮层和海马中5-羟色胺的释放时,我们发现在移除Cat后,L-DOPA(12或100 mg / kg)在两个区域均增强了5-羟色胺的细胞外水平。伴随地,在不存在Ca 2+的情况下,L-DOPA刺激的多巴胺释放部分地以区域依赖的方式持续。血清素再摄取抑制剂西酞普兰(1μM)的局部应用减弱了对L-DOPA(3-12 mg / kg)的反应,以细胞外多巴胺水平衡量,在海马体中最为明显。这些数据强调,低剂量至中等剂量的L-DOPA以区域依赖性方式促进5-羟色胺和多巴胺的非囊泡释放。 (C)2016 Elsevier B.V.和ECNP。版权所有。

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