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阿片类物质对大鼠纹状体切片中苯丙胺刺激的多巴胺释放及浓度的调节作用。

Opioid modulation of amphetamine-stimulated dopamine release and concentration in rat striatal slices.

作者信息

Kolta M G, Bardo M T

机构信息

College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee 32307.

出版信息

Pharmacol Biochem Behav. 1993 Dec;46(4):819-25. doi: 10.1016/0091-3057(93)90207-a.

Abstract

The effects of morphine and naltrexone on amphetamine-stimulated release and total concentration of dopamine (DA) from rat striatal slices in vitro were examined in this study. Adult male Sprague-Dawley rats were sacrificed and the striata were dissected, sliced, and then incubated in buffer solution at 37 degrees C with amphetamine in the presence or absence of various concentrations of morphine, naltrexone (or both), or the dihydroxyphenylalanine (DOPA) decarboxylase inhibitor (NSD-1015). The concentrations of DOPA, DA, and dihydroxyphenylacetic acid (DOPAC) in the tissue slices and buffer media were measured by HPLC/EC. Amphetamine enhanced DA release and also increased total DA concentrations. However, neither morphine nor naltrexone alone altered DA concentration in the media or tissue slices relative to control (no drug added). Moreover, neither morphine nor naltrexone at 1, 10, or 100 microM altered amphetamine-stimulated DA release. However, morphine (1 or 10 microM) inhibited the amphetamine-stimulated increase in total concentration of DA. This effect of morphine was blocked by naltrexone. NSD-1015 alone or in combination with morphine did not alter amphetamine-stimulated DA release, but significantly reduced DA concentration in striatal slices. NSD-1015 alone also increased DOPA accumulation in both media and tissue slices, and this effect was inhibited by the addition of morphine. These results indicate that morphine inhibits the amphetamine-stimulated increase in total DA content, but not the amphetamine-stimulated release of DA.

摘要

本研究检测了吗啡和纳曲酮对体外培养的大鼠纹状体切片中苯丙胺刺激的多巴胺(DA)释放及多巴胺总浓度的影响。处死成年雄性Sprague-Dawley大鼠,解剖取出纹状体,切片后在37℃的缓冲溶液中与苯丙胺一起孵育,同时存在或不存在不同浓度的吗啡、纳曲酮(或两者),或二羟基苯丙氨酸(DOPA)脱羧酶抑制剂(NSD-1015)。通过高效液相色谱/电化学检测法(HPLC/EC)测定组织切片和缓冲液培养基中DOPA、DA和二羟基苯乙酸(DOPAC)的浓度。苯丙胺增强了DA的释放,同时也增加了DA的总浓度。然而,单独使用吗啡或纳曲酮相对于对照组(未添加药物)均未改变培养基或组织切片中DA的浓度。此外,1、10或100微摩尔的吗啡或纳曲酮均未改变苯丙胺刺激的DA释放。但是,吗啡(1或10微摩尔)抑制了苯丙胺刺激引起的DA总浓度增加。吗啡的这种作用被纳曲酮阻断。单独使用NSD-1015或与吗啡联合使用均未改变苯丙胺刺激的DA释放,但显著降低了纹状体切片中DA的浓度。单独使用NSD-1015也增加了培养基和组织切片中DOPA的积累,而添加吗啡可抑制这种作用。这些结果表明,吗啡抑制了苯丙胺刺激引起的DA总含量增加,但不抑制苯丙胺刺激的DA释放。

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