Role of N-methyl-D-aspartate receptors and the nitric oxide pathway in nociception/hyperalgesia elicited by protease-activated receptor-2 activation in mice and rats

被引:23
作者
Kawabata, A [1 ]
Kawao, N
Itoh, H
Shimada, C
Takebe, K
Kuroda, R
Masuko, T
Kataoka, K
Ogawa, S
机构
[1] Kinki Univ, Sch Pharmaceut Sci, Dept Pathophysiol & Therapeut, Higashiosaka, Osaka 5778502, Japan
[2] Kinki Univ, Sch Pharmaceut Sci, Dept Cell Biol, Higashiosaka, Osaka 5778502, Japan
[3] Kinki Univ, Sch Med, Dept Neurosurg, Osaka 5898511, Japan
[4] Sumitomo Pharmaceut Res Ctr, Osaka 5540022, Japan
关键词
protease (proteinase)-activated receptor-2; N-methyl-D-aspartate; nitric oxide; pain; thermal hyperalgesia;
D O I
10.1016/S0304-3940(02)00702-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activation of the peripheral protease-activated receptor-2 (PAR-2) triggers nociceptive behaviour and thermal hyperalgesia in rats. The present study created a novel mouse model for PAR-2-triggered nociception, and then examined the roles of NMIDA receptors and the nitric oxide (NO) pathway in nociceptive processing by PAR-2. Intraplantar administration of the PAR-2 agonist SLIGRL-NH2 elicited nociceptive responses in mice, an effect being more specific in mast cell-depleted mice. This PAR-2-triggered nociception was abolished by the NMDA receptor antagonist MK-801, but not the neuronal NO synthase inhibitor 7-nitro indazole. In contrast, the PAR-2-triggered thermal hyperalgesia in rats was blocked by both agents. Our study thus provides a novel mouse model for PAR-2-mediated nociception, and suggests that NMDA receptors are involved in PAR-2-triggered nociception and hyperalgesia, while NO contributes only to the latter. (C) 2002 Published by Elsevier Science Ireland Ltd.
引用
收藏
页码:349 / 353
页数:5
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