Possible involvement of endogenous nociceptin/orphanin FQ in the pain-related behavioral responses induced by its own metabolite, nociceptin/orphanin FQ(14-17)

被引:5
|
作者
Watanabe, Hiroyuki
Mizoguchi, Hirokazu
Orito, Tohru
Katsuyama, Sou
Yonezawa, Akihiko
Watanabe, Chizuko
Sakurada, Tsukasa
Sakurada, Shinobu
机构
[1] Tohoku Pharmaceut Univ, Dept Physiol & Anat, Aoba Ku, Sendai, Miyagi 9818558, Japan
[2] Daiichi Coll Pharmaceut Sci, Dept Biochem, Fukuoka 8158511, Japan
基金
日本学术振兴会;
关键词
nociceptin; orphanin FQ; ORL-1; receptor; pain; endopeptidase; spinal cord;
D O I
10.1016/j.peptides.2006.11.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 NI 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 maybe mediated through the release of endogenous N/OFQ in the mouse spinal cord. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:670 / 677
页数:8
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