痛觉过敏
前列环素
P物质
医学
前列腺素E2
伤害感受器
药理学
前列腺素
外围设备
敌手
伤害
内分泌学
内科学
化学
麻醉
神经肽
受体
作者
Meire Nakamura-Craig,T.W. Smith
出处
期刊:Pain
[Lippincott Williams & Wilkins]
日期:1989-07-01
卷期号:38 (1): 91-98
被引量:94
标识
DOI:10.1016/0304-3959(89)90078-x
摘要
The hyperalgesic effect of substance P (SP) is usually described as presenting short latency. We now report that multiple injections of sub-threshold doses of SP into the foot pad of a hind paw of rats pre-treated with indomethacin induced a long-lasting hyperalgesia, sensitizing the paw to further challenges with small doses of SP, dopamine or prostacyclin. The sensitizing process also occurred after multiple injections of prostacyclin or prostaglandin E2. The sensitizing effect induced by SP, prostaglandin E2 or prostacyclin is inhibited by pre-treatment with the SP antagonist (d-Arg1, d-Pro2, d-Trp7,9, Leu11)-SP. We suggest that SP has an important role as a modulator in peripheral inflammatory pain by sensitizing nociceptors to its own action and to the action of different mediators. This sensitizing process could also be associated with chronic inflammatory pain.
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