Substance P augments nitric oxide production and gene expression in murine macrophages

被引:26
作者
Jeon, HK
Jung, NP
Choi, IH
Oh, YK
Shin, HC
Gwag, BJ
机构
[1] Yonsei Univ, Dept Biol, Seodaemun Gu, Seoul 120749, South Korea
[2] Yonsei Univ, Dept Biol Sci, Wonju, South Korea
[3] Hallym Univ, Dept Physiol, Chunchun, South Korea
[4] Ajou Univ, Sch Med, Dept Pharmacol, Suwon 441749, South Korea
来源
IMMUNOPHARMACOLOGY | 1999年 / 41卷 / 03期
关键词
substance P; nitric oxide; macrophages; cold stress;
D O I
10.1016/S0162-3109(99)00033-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated the effects of substance P (SP) on nitric oxide (NO) synthase activity in macrophages by measuring the production of nitrite and the expression of inducible NO synthase (iNOS) mRNA and protein. In LPS-activated macrophages, SP stimulated NO production in time and concentration dependent manners. These SP effects were blocked by a specific NX-l receptor antagonist. Furthermore, SP stimulation increased the levels of both iNOS mRNA and iNOS protein. These results demonstrate that SP can increase LPS induced NO production in macrophages by augmenting the induction of iNOS expression. We also examined the role of SP on acute-cold stress induced altered production of NO by mouse peritoneal macrophages. SP enhanced the LPS-induced macrophages NO production from stressed mice relative to the non-stressed mice. These results suggest that SP may have an important modulatory role in production of NO by macrophages. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:219 / 226
页数:8
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