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首页> 外文期刊>European Journal of Pharmacology: An International Journal >The dopamine D3 receptor antagonist PNU-99194A fails to block (+)-7-OH-DPAT substitution for D-amphetamine or cocaine.
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The dopamine D3 receptor antagonist PNU-99194A fails to block (+)-7-OH-DPAT substitution for D-amphetamine or cocaine.

机译:多巴胺D3受体拮抗剂PNU-99194A无法阻止D-苯异丙胺或可卡因的(+)-7-OH-DPAT取代。

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The present study examined the role of dopamine D3 receptor actions in the stimulus generalization produced by (+)-7-OH-DPAT in rats trained to discriminate either D-amphetamine or cocaine from saline. Twelve male Sprague-Dawley rats were trained to discriminate D-amphetamine (1.0 mg/kg) and 12 rats were trained to discriminate cocaine (5.0 mg/kg) from saline in a two-choice, water-reinforced operant procedure. Stimulus generalization tests were administered with the D3 receptor-preferring agonist, (+)-7-hydroxy-N, N-di-n-propyl-2-aminotetralin ((+)-7-OH-DPAT, 0.01-1.0 mg/kg) as well as the D3-preferring antagonist, 5,6-di-methoxy-2-(dipropylamino)indan-hydrochloride (PNU-99194A, 5-40 mg/kg). PNU-99194A (10-40 mg/kg) was also administered in combination with the training dose of D-amphetamine or cocaine to test for antagonism of each training drug cue. Finally, to assess the role of D3 receptor actions in the stimulus generalization produced by (+)-7-OH-DPAT (0.1 mg/kg), PNU-99194A (10, 20 mg/kg) was tested in combination with this compound in each training group. The results showed complete stimulus generalization with (+)-7-OH-DPAT in rats trained to discriminate D-amphetamine, although only partial stimulus generalization was observed with this compound in rats trained to discriminate cocaine. PNU-99194A produced partial substitution for both training drugs, and failed to block the discriminative stimulus effects of either D-amphetamine or cocaine. Moreover, this compound failed to block the stimulus generalization produced by (+)-7-OH-DPAT in rats trained to discriminate D-amphetamine. These results question the importance of D3 receptor actions in the discriminative stimulus effects of psychostimulants and their similarities to (+)-7-OH-DPAT.
机译:本研究检查了多巴胺D3受体作用在由(+)-7-OH-DPAT产生的刺激泛化中的作用,该大鼠受过训练以从盐水中区分D-苯异丙胺或可卡因。训练了十二只雄性Sprague-Dawley大鼠以区分D-苯异丙胺(1.0 mg / kg),训练了十二只大鼠以盐水进行了二选一水强化操作,以将可卡因(5.0 mg / kg)与盐水区分开。给予D3受体优先激动剂(+)-7-羟基-N,N-二-正丙基-2-氨基四氢萘((+)-7-OH-DPAT,0.01-1.0 mg /公斤)以及D3首选拮抗剂5,6-二甲氧基-2-(二丙基氨基)茚满盐酸盐(PNU-99194A,5-40 mg / kg)。也将PNU-99194A(10-40 mg / kg)与D-苯异丙胺或可卡因的训练剂量结合使用,以测试每种训练药物提示的拮抗作用。最后,为了评估D3受体作用在(+)-7-OH-DPAT(0.1 mg / kg)产生的刺激泛化中的作用,将PNU-99194A(10,20 mg / kg)与该化合物组合进行了测试在每个培训小组中。结果表明,在训练区分D-苯异丙胺的大鼠中,用(+)-7-OH-DPAT完全刺激了泛滥,尽管在训练中区分可卡因的大鼠中只观察到了该化合物的部分刺激泛化。 PNU-99194A产生了两种训练药的部分替代,并且未能阻止D-苯异丙胺或可卡因的歧视性刺激作用。此外,该化合物不能阻止由(+)-7-OH-DPAT产生的刺激作用在训练为区分D-苯异丙胺的大鼠中产生。这些结果质疑D3受体作用在精神刺激药的歧视性刺激作用中的重要性及其与(+)-7-OH-DPAT的相似性。

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