首页> 外文期刊>Biological & pharmaceutical bulletin >Suppressive effects of JCICM-6, the extract of an anti-arthritic herbal formula, on the experimental inflammatory and nociceptive models in rodents.
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Suppressive effects of JCICM-6, the extract of an anti-arthritic herbal formula, on the experimental inflammatory and nociceptive models in rodents.

机译:JCICM-6(一种抗关节炎草药配方的提取物)对啮齿动物实验性炎症和伤害模型的抑制作用。

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摘要

JCICM-6, the extract of an anti-arthritic herbal formula composed of medicinal herbs of Sinomenium acutum, Aconitum carmichaeli DEBX., Curcuma Longa L., Paeonia lactiflora PALL., and Paeonia suffruticosa ANDR., was examined in the effectiveness and mechanism in reducing experimentally-induced inflammation and nociception using nine animal models. JCICM-6 was extracted from herbs and purified with Amberlite XAD-7HP adsorbent resin and analyzed with HPLC-fingerprint for quality consistency. In acute inflammatory models, the paw edema of rats was induced by subcutaneous injection of carrageenan or pro-inflammatory mediators, including histamine, serotonin, bradykinin, and prostaglandin E(2) (PGE(2)) into the right hind paws of animals; while the ear edema of mice was induced by applying arachidonic acid or 12-O-tetradecanoylphorbol 13-acetate (TPA) on the ear surface. In nociceptive models, the tail-flick response induced by radiant heat stimulation was measured and the numbers of abdominal writhing episodes of mice induced by intraperitoneal injection of acetic acid were recorded. JCICM-6 orally administered in a range of dosages from 0.438 g to 1.75 g/kg significantly and dose-dependently suppressed the paw edema of rats induced by carrageenan or various pro-inflammatory mediators and the ear edema of mice induced by arachidonic acid or TPA. JCICM-6 also significantly prolonged the reaction time of rats to radiant heat stimulation and reduced the numbers of writhing episodes of mice. These results indicated that JCICM-6 possesses significant anti-inflammatory and analgesic effects, which implies that it would be a potential candidate for further investigation as a new anti-arthritic botanical drug for humans.
机译:研究了JCICM-6(一种抗关节炎草药配方的提取物)的功效和作用机理,该草药配方由尖竹,刺乌头,姜黄,Cur药和Pa药组成。使用九种动物模型减少实验性炎症和伤害感受。从草药中提取JCICM-6,并用Amberlite XAD-7HP吸附树脂纯化,并用HPLC指纹分析质量一致性。在急性炎症模型中,通过向动物右后爪皮下注射角叉菜胶或促炎介质,包括组胺,5-羟色胺,缓激肽和前列腺素E(2)(PGE(2))诱导大鼠的爪水肿。而通过在耳朵表面施加花生四烯酸或12-O-十四烷酰佛波醇13-乙酸盐(TPA)诱导小鼠的耳朵水肿。在伤害模型中,测量了辐射热刺激引起的甩尾反应,并记录了腹膜内注射乙酸引起的小鼠腹部扭动发作的次数。 JCICM-6的口服剂量范围从0.438 g至1.75 g / kg,显着剂量依赖性地抑制了角叉菜胶或各种促炎介质诱导的大鼠爪水肿以及花生四烯酸或TPA诱导的小鼠耳部水肿。 JCICM-6还显着延长了大鼠对辐射热刺激的反应时间,并减少了小鼠扭体发作的次数。这些结果表明,JCICM-6具有显着的抗炎和止痛作用,这意味着它可能作为一种新型的人类抗关节炎植物药而进一步研究。

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