首页> 外文期刊>Peptides: An International Journal >Possible involvement of endogenous nociceptin/orphanin FQ in the pain-related behavioral responses induced by its own metabolite, nociceptin/orphanin FQ(14-17).
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Possible involvement of endogenous nociceptin/orphanin FQ in the pain-related behavioral responses induced by its own metabolite, nociceptin/orphanin FQ(14-17).

机译:内源性伤害感受器/孤啡肽FQ可能参与其自身代谢产物伤害感受器/孤啡肽FQ引起的疼痛相关行为反应(14-17)。

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Nociceptin/orphanin FQ(14-17) (N/OFQ(14-17)) is one of the major fragments that are released from N/OFQ, an endogenous ligand for the opioid receptor like-1 (ORL-1) receptor by endopeptidase 24.11. In the present study, we determined the pharmacological profiles of N/OFQ(14-17) on pain-related behavioral responses in the mouse. Intrathecal (i.t.) administration of N/OFQ(14-17) (5-160 pmol) evoked pain-related behaviors, and these behavioral responses were reduced by i.t. co-administration of an ORL-1 receptor antagonist, [Nphe(1)]N/OFQ(1-13)NH2 (4 pmol). However, in the ligand-binding receptor assay, N/OFQ(14-17) had no affinity for the ORL-1 receptor. Furthermore, i.t. pretreatment with an antiserum against N/OFQ (1:50) diminished the N/OFQ(14-17)-induced pain-related behaviors, suggesting that endogenous N/OFQ is involved in their expression. Therefore, N/OFQ(14-17)-induced pain-related behaviors may be mediated through the release of endogenous N/OFQ in the mouse spinal cord.
机译:Nociceptin / orphanin FQ(14-17)(N / OFQ(14-17))是从N / OFQ释放的主要片段之一,N / OFQ是阿片受体样1(ORL-1)受体的内源性配体内肽酶24.11。在本研究中,我们确定了N / OFQ(14-17)对小鼠疼痛相关行为反应的药理作用。鞘内(i.t.)施用N / OFQ(14-17)(5-160 pmol)引起疼痛相关行为,并且这些行为反应因i.t.而降低。 ORL-1受体拮抗剂[Nphe(1)] N / OFQ(1-13)NH2(4 pmol)的共同给药。但是,在配体结合受体测定中,N / OFQ(14-17)对ORL-1受体没有亲和力。此外,用抗N / OFQ的抗血清(1:50)进行预处理可减少N / OFQ(14-17)诱导的疼痛相关行为,表明内源性N / OFQ参与其表达。因此,N / OFQ(14-17)诱导的疼痛相关行为可能是通过在小鼠脊髓中释放内源性N / OFQ介导的。

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