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孤啡肽受体敲除大鼠:体内外研究。

Nociceptin/orphanin FQ receptor knockout rats: in vitro and in vivo studies.

机构信息

Department of Experimental and Clinical Medicine, University of Ferrara, Ferrara, Italy.

出版信息

Neuropharmacology. 2011 Mar;60(4):572-9. doi: 10.1016/j.neuropharm.2010.12.010. Epub 2010 Dec 22.

Abstract

Nociceptin/orphanin FQ (N/OFQ) regulates several biological functions via selective activation of the N/OFQ peptide (NOP) receptor. Recently knockout rats for the NOP receptor gene (NOP(-/-)) have been generated; these animals were used in the present study to investigate their emotional (open field, elevated plus maze, and forced swimming test), locomotor (drag and rotarod test), and nociceptive (plantar and formalin test) phenotypes in comparison with their NOP(+/+) littermates. In addition, N/OFQ sensitivity has been assessed in electrically stimulated vas deferens tissues taken from NOP(+/+) and NOP(-/-) rats. In the elevated plus maze and forced swimming tests NOP(-/-) rats showed anxiety- and anti-depressant-like phenotype, respectively. No differences were found in the open field test. NOP(-/-) rats outperformed their NOP(+/+) littermates in two motor behaviour assays. Genetic ablation of the NOP receptor gene produced a statistically significant increase in nociceptive behaviour of the mutant rats in the formalin test. Finally, in the electrically stimulated rat vas deferens taken from NOP(+/+) tissues, N/OFQ inhibited in a concentration-dependent manner the electrically induced twitches while the peptide was inactive in tissues taken from NOP(-/-) animals. These results, in line with previous findings obtained with selective NOP receptor antagonists in mice and rats and with mouse knockout studies, clearly indicate that endogenous N/OFQ-NOP receptor signalling plays an important role in controlling anxiety- and mood-related behaviours, exercise-driven locomotor activity and nociception. These observations are relevant for defining the therapeutic indications (and contraindications) of NOP receptor antagonists.

摘要

孤啡肽(Nociceptin/orphanin FQ,N/OFQ)通过选择性激活孤啡肽肽(NOP)受体来调节多种生物学功能。最近,已经产生了 NOP 受体基因敲除大鼠(NOP(-/-));在本研究中,将这些动物与它们的 NOP(+/+)同窝仔鼠进行比较,以研究它们的情感(旷场、高架十字迷宫和强迫游泳试验)、运动(拖拽和旋转棒试验)和痛觉(足底和福尔马林试验)表型。此外,还评估了来自 NOP(+/+)和 NOP(-/-)大鼠的电刺激输精管组织中 N/OFQ 的敏感性。在高架十字迷宫和强迫游泳试验中,NOP(-/-)大鼠分别表现出焦虑和抗抑郁样表型。在旷场试验中未发现差异。在两项运动行为测定中,NOP(-/-)大鼠的表现优于它们的 NOP(+/+)同窝仔鼠。NOP 受体基因的遗传缺失导致突变大鼠在福尔马林试验中的痛觉行为显著增加。最后,在来自 NOP(+/+)组织的电刺激大鼠输精管中,N/OFQ 以浓度依赖性方式抑制电诱导的抽搐,而该肽在来自 NOP(-/-)动物的组织中无活性。这些结果与先前在小鼠和大鼠中使用选择性 NOP 受体拮抗剂以及小鼠敲除研究获得的结果一致,清楚地表明内源性 N/OFQ-NOP 受体信号在控制焦虑和情绪相关行为、运动驱动的运动活动和痛觉方面发挥着重要作用。这些观察结果对于确定 NOP 受体拮抗剂的治疗适应症(和禁忌症)具有重要意义。

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