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首页> 外文期刊>Peptides: An International Journal >Neuropeptide S inhibits the acquisition and the expression of conditioned place preference to morphine in mice.
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Neuropeptide S inhibits the acquisition and the expression of conditioned place preference to morphine in mice.

机译:神经肽S抑制了小鼠中吗啡的获得和条件位置偏爱的表达。

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Neuropeptide S (NPS), a recently identified bioactive peptide, was reported to regulate arousal, anxiety, motoring and feeding behaviors. NPS precursor and NPS receptor mRNA were found in the amygdala, the ventral tegmental area (VTA) and the substantia nigra, the area thought to modulate rewarding properties of drugs. In the present study, we examined the influence of NPS on the rewarding action of morphine, using the unbiased conditioned place preference (CPP) paradigm. Morphine (1, 3 and 6nmol, i.c.v.) induced a significant place preference. For testing the effect of NPS on the acquisition of morphine CPP, mice were given the combination of NPS and morphine on the conditioning days, and without drug treatment on the followed test day. To study the effect of NPS on the expression of morphine CPP, mice received the treatment of saline/morphine on the conditioning days, and NPS on the test day, 15min before the placement in the CPP apparatus. Our results showed that NPS (0.3-10nmol) alone neither induced place preference nor aversion, however, NPS (1 and 3nmol) blocked the acquisition of CPP induced by 3nmol morphine, and acquisition of 6nmol morphine-induced CPP was also reduced by NPS (6 and 10nmol). Moreover, the expression of CPP induced by 6nmol morphine was also inhibited by NPS (0.1, 1 and 10nmol). These results revealed the involvement of NPS in rewarding activities of morphine, and demonstrated the interaction between NPS system and opioid system for the first time.
机译:据报道,神经肽S(NPS)是最近发现的一种生物活性肽,可调节唤醒,焦虑,运动和进食行为。 NPS前体和NPS受体mRNA在杏仁核,腹侧被膜区(VTA)和黑质中被发现,该区域被认为可调节药物的奖励特性。在本研究中,我们使用无偏的条件性位置偏爱(CPP)范式检查了NPS对吗啡奖励作用的影响。吗啡(1、3和6nmol,i.c.v。)引起明显的位置偏爱。为了测试NPS对获得吗啡CPP的作用,在调理日给小鼠NPS和吗啡的组合,在随后的测试日不给予药物治疗。为了研究NPS对吗啡CPP表达的影响,小鼠在条件日接受生理盐水/吗啡的治疗,在测试日(放置于CPP仪器之前15分钟)接受NPS的处理。我们的结果表明,单独的NPS(0.3-10nmol)既不引起位置偏爱也不引起厌恶,但是NPS(1和3nmol)阻止了3nmol吗啡诱导的CPP的获得,并且6nmol吗啡诱导的CPP的获得也被NPS减少了6和10nmol)。此外,NPS(0.1、1和10nmol)也抑制了6nmol吗啡诱导的CPP表达。这些结果揭示了NPS参与吗啡的奖励活动,并首次证明了NPS系统与阿片样物质系统之间的相互作用。

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