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首页> 外文期刊>Life sciences >(-)-STEPHOLIDINE ACTS AS A D-1 PARTIAL AGONIST ON FIRING ACTIVITY OF SUBSTANTIA NIGRA PARS RETICULATA NEURONS IN 6-HYDROXYDOPAMINE-LESIONED RATS
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(-)-STEPHOLIDINE ACTS AS A D-1 PARTIAL AGONIST ON FIRING ACTIVITY OF SUBSTANTIA NIGRA PARS RETICULATA NEURONS IN 6-HYDROXYDOPAMINE-LESIONED RATS

机译:(-)-甜菊碱作为D-1局部激动剂对6-羟基多巴胺致病大鼠黑质黑质网状神经元放电活性的影响

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(-)-Stepholidine (SPD), a novel dopamine (DA) D-1 and/or D-2 receptor antagonist in normosensitive animals, shows agonistic effects on D-1 receptors in rotational behavior of 6-hydroxydopamine (6-OHDA)-lesioned rats. To further characterize the pharmacological properties of SPD, we investigated the effects of SPD on firing activity of substantia nigra pars reticulata (SNR) neurons in different sensitive models. In control rats, the selective D-1 agonist SKF38393 (4 mg/kg, i.v.) induced inconsistent. changes (i.e. increase, decrease or no change) in firing of SNR neurons. These effects were completely antagonized by SPD (i.v.), regardless of the changes induced by SKF38393. SPD (4 mg/kg), per se, increased firing by 30.9 +/- 14.4%. In reserpinized rats, SKF38393 also induced SPD-reversible inconsistent changes as in control rats. Nevertheless, SPD per se produced no alteration in firing of SNR neurons. In 6-OHDA-lesioned rats, 5/6 SNR neurons were inhibited by SKF38393. The inhibition was completely abolished by Sch23390, a selective D-1 antagonist (0.5-2 mg/kg), but partially reversed by SPD (1-16 mg/kg). Moreover, SPD (4 mg/kg) itself caused SNR increased or decreased neuron firing, and these effects were completely reversed by Sch23390 (0.5-2 mg/kg) in 8/12 neurons recorded. These results suggest that SPD acts as a partial agonist to D-1 receptors in 6-OHDA-lesioned rats, but as an antagonist to D-1 receptors in normal and reserpinized rats. [References: 26]
机译:(-)-Stepholidine(SPD)是常感性动物中的新型多巴胺(DA)D-1和/或D-2受体拮抗剂,在6-羟基多巴胺(6-OHDA)的旋转行为中对D-1受体具有激动作用病变的大鼠。为了进一步表征SPD的药理特性,我们研究了SPD对不同敏感性模型中黑质网状(SNR)神经元放电活性的影响。在对照大鼠中,选择性D-1激动剂SKF38393(4mg / kg,静脉内)诱导不一致。 SNR神经元放电的变化(即增加,减少或没有变化)。不论SKF38393引起的变化如何,SPD(i.v.)都完全拮抗了这些作用。 SPD(4 mg / kg)本身可提高30.9 +/- 14.4%的发射率。在再固定化的大鼠中,SKF38393还诱导SPD可逆的不一致变化,就像在对照大鼠中一样。尽管如此,SPD本身在SNR神经元放电方面并未产生任何改变。在6-OHDA损伤的大鼠中,SKF38393抑制了5/6 SNR神经元。选择性D-1拮抗剂(0.5-2 mg / kg)Sch23390完全消除了抑制作用,但SPD(1-16 mg / kg)则部分抵消了抑制作用。此外,SPD(4 mg / kg)本身会导致SNR增加或减少神经元放电,而在记录的8/12神经元中,Sch23390(0.5-2 mg / kg)完全抵消了这些影响。这些结果表明,SPD在6-OHDA损伤的大鼠中充当D-1受体的部分激动剂,但在正常和再固定化的大鼠中充当D-1受体的拮抗剂。 [参考:26]

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