阿片能
育亨宾
药理学
化学
甲硫醚
芦丁
(+)-纳洛酮
敌手
5-羟色胺能
受体拮抗剂
类阿片
受体
止痛药
伤害
传统医学
医学
血清素
生物化学
出处
期刊:한국응용생명화학회지
[Springer Nature]
日期:2010-10-01
卷期号:53 (5): 593-597
被引量:8
标识
DOI:10.3839/jksabc.2010.091
摘要
Antinociceptive profiles of Ruta graveolens L extract were examined in ICR mice. R. graveolens L extract administered orally (200 mg/kg) showed an antinociceptive effect as measured by the tailflick and hot-plate tests and attenuated the writhing numbers in the acetic acid-induced writhing test. Cumulative nociceptive response time for intrathecal (i.t.) injection of substance P (0.7 μg) was decreased by the extract. Intraperitoneal (i.p.) pretreatment with naloxone (opioid receptor antagonist) or yohimbine (α2-adrenergic receptor antagonist) attenuated antinociceptive effect induced by the extract in the writhing test. However, methysergide (5-HT serotonergic receptor antagonist) did not affect antinociception induced by the extract in the writhing test. These results suggest that R. graveolens L extract exerts antinociceptive property in various pain models. Furthermore, this antinociceptive effect of R. graveolens L extract may be mediated by opioidergic and α2-adrenergic receptors, but not by serotonergic receptors.
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