Characterization of intrathecally administered hemokinin-1-induced nociceptive behaviors in mice

被引:13
作者
Watanabe, Chizuko [1 ]
Mizoguchi, Hirokazu [1 ]
Yonezawa, Akihiko [1 ]
Sakurada, Shinobu [1 ]
机构
[1] Tohoku Pharmaceut Univ, Dept Physiol & Anat, Aoba Ku, Sendai, Miyagi 9818558, Japan
基金
日本学术振兴会;
关键词
Hemokinin-1; Tachykinin; Nociceptive behavior; Pain; Spinal cord; TACHYKININ NK1 RECEPTOR; SUBSTANCE-P; HEMOKININ; ISOFORMS;
D O I
10.1016/j.peptides.2010.04.025
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
Hemokinin-1 is a novel mammalian tachykinin cloned from mouse bone marrow. At present, pharmacological profile and physiological role of hemokinin-1 are still unclear. In the present study, we found that intrathecal (i.t.) administration of hemokinin-1 (0.00625-1.6 nmol) induced nociceptive responses consisting of scratching, biting and licking, which resemble substance P-induced behavioral responses in mice. The behaviors evoked by low-dose of hemokinin-1 (0.0125 nmol) were dose-dependently inhibited by it. co-administration of CP-99,994, a non-peptidic tachykinin NK1 receptor antagonist, whereas high-dose of hemokinin-1 (0.1 nmol)-induced behaviors were not affected. Moreover, sendide, a peptidic tachykinin NK1 receptor antagonist, failed to reduce the behavioral responses of both low- and high-dose of hemokinin-1. In contrast, substance P-induced behaviors were completely suppressed by both CP-99,994 and sendide. These results suggest that hemokinin-1 plays an important role in pain transmission at spinal cord. Moreover, the mechanism of hemokinin-1 -induced nociceptive behaviors may be dose-dependent, and distinct from substance P-induced nociceptive behaviors. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1613 / 1616
页数:4
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