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血清素-γ-氨基丁酸相互作用调节摇头丸诱导的中脑边缘多巴胺释放。

Serotonin-GABA interactions modulate MDMA-induced mesolimbic dopamine release.

作者信息

Bankson Michael G, Yamamoto Bryan K

机构信息

Laboratory of Neurochemistry, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, Massachusetts 02118, USA.

出版信息

J Neurochem. 2004 Nov;91(4):852-9. doi: 10.1111/j.1471-4159.2004.02763.x.

DOI:10.1111/j.1471-4159.2004.02763.x
PMID:15525339
Abstract

3,4,-Methylenedioxymethamphetamine (MDMA; 'ecstasy') acts at monoamine nerve terminals to alter the release and re-uptake of dopamine and 5-HT. The present study used microdialysis in awake rats to measure MDMA-induced changes in extracellular GABA in the ventral tegmental area (VTA), simultaneous with measures of extracellular dopamine (DA) in the nucleus accumbens (NAC) shell. (+)-MDMA (0, 2.5, 5 and 10 mg/kg, i.p.) increased GABA efflux in the VTA with a bell-shaped dose-response. This increase was blocked by application of TTX through the VTA probe. MDMA (5 mg/kg) increased 5-HT efflux in VTA by 1037% (p < 0.05). The local perfusion of the 5-HT(2B/2C) antagonist SB 206553 into the VTA reduced VTA GABA efflux after MDMA from a maximum of 229% to a maximum of 126% of basal values (p < 0.05), while having no effect on basal extracellular GABA concentrations. DA concentrations measured simultaneously in the NAC shell were increased from a maximum of 486% to 1320% (p < 0.05). The selective DA releaser d-amphetamine (AMPH) (4 mg/kg) also increased VTA GABA efflux (180%), did not alter 5-HT and increased NAC DA (875%) (p < 0.05), but the perfusion of SB 206553 into the VTA failed to alter these effects. These results suggest that MDMA-mediated increases in DA within the NAC shell are dampened by increases in VTA GABA subsequent to activation of 5-HT(2B/2C) receptors in the VTA.

摘要

3,4-亚甲基二氧甲基苯丙胺(摇头丸;“摇头丸”)作用于单胺能神经末梢,改变多巴胺和5-羟色胺的释放及再摄取。本研究采用微透析技术,在清醒大鼠中测量摇头丸诱导的腹侧被盖区(VTA)细胞外γ-氨基丁酸(GABA)的变化,同时测量伏隔核(NAC)壳层细胞外多巴胺(DA)的变化。(+)-摇头丸(0、2.5、5和10毫克/千克,腹腔注射)以钟形剂量反应增加VTA中的GABA流出。通过VTA探针应用河豚毒素(TTX)可阻断这种增加。摇头丸(5毫克/千克)使VTA中的5-羟色胺流出增加1037%(p<0.05)。将5-羟色胺(2B/2C)拮抗剂SB 206553局部灌注到VTA中,可使摇头丸作用后的VTA GABA流出从基础值的最大229%降至最大126%(p<0.05),而对基础细胞外GABA浓度无影响。同时在NAC壳层测量的DA浓度从最大486%增加到1320%(p<0.05)。选择性DA释放剂右旋苯丙胺(AMPH)(4毫克/千克)也增加了VTA GABA流出(180%),不改变5-羟色胺,并增加了NAC DA(875%)(p<0.05),但将SB 206553灌注到VTA中未能改变这些作用。这些结果表明,摇头丸介导的NAC壳层中DA的增加被VTA中5-羟色胺(2B/2C)受体激活后VTA中GABA的增加所抑制。

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