首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Dynorphin modulates dopamine D1-receptor mediated turning behavior in 6-hydroxydopamine-lesioned rats.
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Dynorphin modulates dopamine D1-receptor mediated turning behavior in 6-hydroxydopamine-lesioned rats.

机译:强啡肽在6-羟基多巴胺损伤的大鼠中调节多巴胺D1受体介导的转弯行为。

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We investigated if the potentiated turning response to a challenge with the partial dopamine D1 receptor agonist SKF-38393, as seen after priming with L-dihydroxyphenylalanine (DOPA) of unilaterally 6-hydroxydopamine-lesioned rats, can be modulated by infusion of dynorphin A (1-17) in the striatum. Seventeen days after the 6-hydroxydopamine lesion, rats received intrastriatal dynorphin (0. 08 or 3.85 microg) followed by L-DOPA (50 mg/kg i.p.) and were challenged 3 days later with SKF-38393 (3.0 mg/kg s.c.). Compared to controls, the lower dose of dynorphin caused an earlier onset of turning, while the higher dose decreased the response to SKF-38393. These findings suggest a dose-dependent modulatory role for striatal dynorphin in L-DOPA-priming of a D1-mediated behavioral response.
机译:我们调查了用多巴胺D1受体激动剂SKF-38393对L-二羟基苯丙氨酸(DOPA)引发的单侧6-羟基多巴胺损伤大鼠的激发后增强的转弯反应是否可以通过输注强啡肽A( 1-17)在纹状体中。 6-羟基多巴胺损伤后第17天,大鼠接受纹状体内强啡肽(0. 08或3.85 microg),然后接受L-DOPA(50 mg / kg腹膜内),并在3天后用SKF-38393(3.0 mg / kg sc)攻击。与对照组相比,较低剂量的强啡肽导致更早发作,而较高剂量则降低了对SKF-38393的反应。这些发现表明在D1介导的行为反应的L-DOPA启动中,纹状体强啡肽的剂量依赖性调节作用。

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