Nishi M, Houtani T, Noda Y, Mamiya T, Sato K, Doi T, Kuno J, Takeshima H, Nukada T, Nabeshima T, Yamashita T, Noda T, Sugimoto T
Department of Neurochemistry, Tokyo Institute of Psychiatry, Kamikitazawa, Japan.
EMBO J. 1997 Apr 15;16(8):1858-64. doi: 10.1093/emboj/16.8.1858.
In the G-protein-coupled receptor superfamily, the opioid receptor subfamily is constituted of the three distinct opioid receptors (namely delta-, mu- and kappa-subtypes) and the receptor for nociceptin (also designated orphaninFQ). The members of the opioid receptor subfamily were known to mediate a variety of cellular inhibitory effects. The three opioid receptors are known to play central roles in mediating analgesia and many other physiological activities; however, the nociceptin receptor was identified recently and less is known about its physiological roles. Here we report the generation and characterization of mice lacking the nociceptin receptor. The knockout mice showed no significant differences in nociceptive threshold and locomotor activity compared with control mice, but they lost nociceptin-induced behavioral responses. These results indicate that the nociceptin system is not essential for regulation of nociception or locomotor activity. On the other hand, we found insufficient recovery of hearing ability from the adaptation to sound exposure in the mutant mice. Thus, the nociceptin system appears to participate in the regulation of the auditory system.
在G蛋白偶联受体超家族中,阿片受体亚家族由三种不同的阿片受体(即δ、μ和κ亚型)以及孤啡肽受体(也称为孤啡肽FQ)组成。已知阿片受体亚家族的成员介导多种细胞抑制作用。已知这三种阿片受体在介导镇痛和许多其他生理活动中起核心作用;然而,孤啡肽受体是最近才被鉴定出来的,对其生理作用了解较少。在此,我们报告了缺乏孤啡肽受体的小鼠的产生和特性。与对照小鼠相比,基因敲除小鼠在痛觉阈值和运动活性方面没有显著差异,但它们失去了孤啡肽诱导的行为反应。这些结果表明,孤啡肽系统对于痛觉或运动活性的调节并非必不可少。另一方面,我们发现突变小鼠从声音暴露适应中恢复听力的能力不足。因此,孤啡肽系统似乎参与了听觉系统的调节。