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首页> 外文期刊>Japanese Journal of Pharmacology >Effects of Neurotransmitters or Drugs on the in Vivo Release of Dopamine and Its Metabolites
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Effects of Neurotransmitters or Drugs on the in Vivo Release of Dopamine and Its Metabolites

机译:神经递质或药物对多巴胺及其代谢物体内释放的影响

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References(39) Cited-By(15) The effects of neurotransmitters or drugs on the release of endogenous dopamine (DA) and extracellular levels of its metabolites, 3, 4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), were examined in vivo by intracerebral dialysis. A dialysis tube was implanted stereotaxically through bilateral caudate nuclei of rats and perfused with the Ringer solution. Amounts of DA, DOPAC and HVA in the perfusates were measured by high performance liquid chromatography (HPLC) with electrochemical detection. The basal level of DA was 2.76±0.64 pg/min, whereas the levels of DOPAC and HVA were 218.7±20.7 and 142.4±10.6 pg/min, respectively. Apomorphine (4 mg/kg, i.v.) reduced the efflux of DA and its metabolites. Haloperidol (0.4 mg/kg, i.v.) did not change DA release and produced only a minor increase of its metabolites. This increase of metabolites was inhibited by pargyline. Met-enkephalin (10-4 M), substance P (10-4 M) and acetylcholine chloride (10-4 M) added to the perfusing medium increased the release of DA. Met-enkephalin also increased the release of DOPAC. γ-Amino-n-butyric acid (GABA, 10-4 M) reduced the release of DOPAC and HVA when added to the perfusing medium. Thyrotropin releasing hormone (TRH, 5 mg/kg, i.v.) increased the release of HVA. These findings indicated that different mechanisms mediated effects of neurotransmitters or drugs on the release and metabolism of DA in the rat striatum.
机译:参考文献(39)被引用的文献(15)研究了神经递质或药物对内源多巴胺(DA)释放及其代谢产物3,4-二羟基苯乙酸(DOPAC)和高香草酸(HVA)的细胞外水平的影响在体内通过脑内透析。将透析管通过大鼠的双侧尾状核进行立体定位植入,并灌注林格液。通过高效液相色谱(HPLC)进行电化学检测,测定灌注液中DA,DOPAC和HVA的含量。 DA的基础水平是2.76±0.64 pg / min,而DOPAC和HVA的水平分别是218.7±20.7和142.4±10.6 pg / min。阿扑吗啡(4 mg / kg,静脉内)降低了DA及其代谢产物的外排量。氟哌啶醇(0.4 mg / kg,静脉内)不会改变DA的释放,只会产生少量的代谢产物。代谢产物的这种增加被精氨酸抑制。添加到灌注培养基中的脑啡肽(10-4 M),物质P(10-4 M)和乙酰胆碱(10-4 M)增加了DA的释放。 Met-脑啡肽还增加了DOPAC的释放。当添加到灌注介质中时,γ-氨基正丁酸(GABA,10-4 M)减少了DOPAC和HVA的释放。促甲状腺激素释放激素(TRH,5 mg / kg,i.v.)增加了HVA的释放。这些发现表明,不同的机制介导了神经递质或药物对大鼠纹状体中DA的释放和代谢的影响。

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