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神经肽S通过选择性激活神经肽S受体降低小鼠在定居者/入侵者测试中的攻击性。

Neuropeptide S reduces mouse aggressiveness in the resident/intruder test through selective activation of the neuropeptide S receptor.

作者信息

Ruzza Chiara, Asth Laila, Guerrini Remo, Trapella Claudio, Gavioli Elaine C

机构信息

Department of Medical Sciences, Section of Pharmacology and National Institute of Neuroscience, University of Ferrara, Via Fossato di Mortara 19, 44121 Ferrara, Italy.

Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, Brazil.

出版信息

Neuropharmacology. 2015 Oct;97:1-6. doi: 10.1016/j.neuropharm.2015.05.002. Epub 2015 May 13.

Abstract

Neuropeptide S (NPS) regulates various biological functions by selectively activating the NPS receptor (NPSR). In particular NPS evokes robust anxiolytic-like effects in rodents together with a stimulant and arousal promoting action. The aim of the study was to investigate the effects of NPS on the aggressiveness of mice subjected to the resident/intruder test. Moreover the putative role played by the endogenous NPS/NPSR system in regulating mice aggressiveness was investigating using mice lacking the NPSR receptor (NPSR(-/-)) and the NPSR selective antagonists [(t)Bu-D-Gly(5)]NPS and SHA 68. NPS (0.01-1 nmol, icv) reduced, in a dose dependent manner, both the time that resident mice spent attacking the intruder mice and their number of attacks, producing pharmacological effects similar to those elicited by the standard anti-aggressive drug valproate (300 mg/kg, ip). This NPS effect was evident in NPSR wild type (NPSR(+/+)) mice but completely disappeared in NPSR(-/-) mice. Moreover, NPSR(-/-) mice displayed a significantly higher time spent attacking than NPSR(+/+) mice. [(t)Bu-D-Gly(5)]NPS (10 nmol, icv) did not change the behavior of mice in the resident/intruder test but completely counteracted NPS effects. SHA 68 (50 mg/kg, ip) was inactive per se and against NPS. In conclusion, this study demonstrated that NPS produces anti-aggressive effects in mice through the selective activation of NPSR and that the endogenous NPS/NPSR system can exert a role in the control of aggressiveness levels under the present experimental conditions.

摘要

神经肽 S(NPS)通过选择性激活 NPS 受体(NPSR)来调节多种生物学功能。特别是,NPS 在啮齿动物中引发强烈的抗焦虑样作用,同时具有刺激和促进觉醒的作用。本研究的目的是调查 NPS 对接受定居者/入侵者测试的小鼠攻击性的影响。此外,使用缺乏 NPSR 受体(NPSR(-/-))的小鼠以及 NPSR 选择性拮抗剂[(t)Bu-D-Gly(5)]NPS 和 SHA 68,研究内源性 NPS/NPSR 系统在调节小鼠攻击性中所起的假定作用。NPS(0.01 - 1 nmol,脑室内注射)以剂量依赖性方式减少了定居小鼠攻击入侵者小鼠的时间及其攻击次数,产生的药理作用与标准抗攻击药物丙戊酸盐(300 mg/kg,腹腔注射)所引发的作用相似。这种 NPS 效应在 NPSR 野生型(NPSR(+/+))小鼠中明显,但在 NPSR(-/-)小鼠中完全消失。此外,NPSR(-/-)小鼠表现出比 NPSR(+/+)小鼠显著更长的攻击时间。[(t)Bu-D-Gly(5)]NPS(10 nmol,脑室内注射)在定居者/入侵者测试中未改变小鼠的行为,但完全抵消了 NPS 的作用。SHA 68(50 mg/kg,腹腔注射)本身无活性,且对 NPS 也无作用。总之,本研究表明 NPS 通过选择性激活 NPSR 在小鼠中产生抗攻击作用,并且在当前实验条件下,内源性 NPS/NPSR 系统可在控制攻击水平中发挥作用。

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