Koga Kazumi, Ichikawa Daisuke, Nambu Hirohide, Azuma-Kanoh Tomoko, Sakai Naoko, Takaki-Kawagoe Hiroko, Ozaki Satoshi, Ohta Hisashi
Pharmacology, Tsukuba Research Institute, Banyu Pharmaceutical Co., Ltd., 3 Okubo, Tsukuba, Ibaraki 300-2611, Japan.
Genes Genet Syst. 2009 Oct;84(5):319-25. doi: 10.1266/ggs.84.319.
We succeeded in cloning the rhesus monkey nociceptin/orphanin FQ peptide (NOP) receptor. The nucleotide sequence and amino acid sequence of the rhesus monkey NOP receptor were 95.9% and 97.8%, respectively, identical to the human NOP receptor. There was no significant difference between the rhesus monkey NOP receptor and the human NOP receptor in the binding affinity of [(125)I] [Thy(14)]nociceptin and the binding of [(35)S]guanosine 5'-O-(gamma thio)triphospate ([(35)S]GTPgammaS) stimulated by nociceptin/orphanin FQ (N/OFQ). A selective NOP receptor antagonist, 1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one ((+)-J-113397) inhibited the [(35)S]GTPgammaS binding activated by N/OFQ using the membrane of the rhesus monkey NOP receptor. The antagonistic activity of (+)-J-113397 to the rhesus monkey NOP receptor was comparable to that to the human NOP receptor. Thus, N/OFQ acts via activation of the NOP receptor in both human and rhesus monkeys without significant species differences.
我们成功克隆了恒河猴孤啡肽/孤啡肽FQ肽(NOP)受体。恒河猴NOP受体的核苷酸序列和氨基酸序列分别与人类NOP受体有95.9%和97.8%的同源性。在[(125)I][Thy(14)]孤啡肽的结合亲和力以及孤啡肽/孤啡肽FQ(N/OFQ)刺激的[(35)S]鸟苷5'-O-(γ硫代)三磷酸([(35)S]GTPγS)结合方面,恒河猴NOP受体与人类NOP受体之间没有显著差异。一种选择性NOP受体拮抗剂1-[(3R,4R)-1-环辛基甲基-3-羟甲基-4-哌啶基]-3-乙基-1,3-二氢-2H-苯并咪唑-2-酮((+)-J-113397)使用恒河猴NOP受体膜抑制了N/OFQ激活的[(35)S]GTPγS结合。(+)-J-113397对恒河猴NOP受体的拮抗活性与人NOP受体相当。因此,N/OFQ通过激活NOP受体在人类和恒河猴中发挥作用,且无明显种属差异。