Arzi A, Namjouyan F, Sarahroodi S, Khorasgani Z Nazari, Macvandi E
Department of Pharmacology and Toxicology, School of Pharmacy, Ahwaz Jundishapur University of Medical Sciences, Golestan Blvd., Ahwaz, Iran.
Pak J Biol Sci. 2011 Dec 1;14(23):1066-9. doi: 10.3923/pjbs.2011.1066.1069.
Antinociceptive and anti-inflammatory activities of hydroalcoholic extract of Teucrium Oliverianum were investigated by formalin test model. This study was conducted in on the male Wistar rats, weighting 150-180 g. The animals were divided into seven groups (n = 7) and received 200, 400, 600 and 800 mg kg(-1) of hydroalcoholic extract of teucrium oliverianum intraperitoneally, respectively. Negative control group received normal saline (5 mL kg(-1)) and the positive control groups received 2.5 mg kg(-1) morphine and 300 mg kg(-1) aspirin, intraperitoneally respectively. The results showed that all doses of extract have significant analgesic effect (p < 0.05) in all studies times in comparison with negative control. The best result achieved with 600 mg kg(-1) of extract. The result revealed that the analgesic effect of the extract (600 mg kg(-1)) \was less than aspirin (300 mg kg(-1)) on the second phase of pain and less than morphine (2.5 mg kg(-1)) in both phases of the pain, more than aspirin in first phase of pain. One group of animals was treated with naloxone (1 mg kg(-1), i.p.) and suitable dose of extract (600 mg kg(-1), i.p.). Also, Naloxone inhibited analgesic effect of alcoholic extract of Teucrium Oliverianum. It can be concluded that the alcoholic extract of Teucrium oliverianum may exert its effect through opioid receptors, stimulating GABAergic system or promotes the release of endogenous opipeptides or decreasing free radicals.
通过福尔马林试验模型研究了奥利维香科叶草水醇提取物的抗伤害感受和抗炎活性。本研究以体重150 - 180 g的雄性Wistar大鼠为对象。将动物分为七组(n = 7),分别腹腔注射200、400、600和800 mg/kg的奥利维香科叶草水醇提取物。阴性对照组给予生理盐水(5 mL/kg),阳性对照组分别腹腔注射2.5 mg/kg吗啡和300 mg/kg阿司匹林。结果表明,与阴性对照组相比,所有剂量的提取物在所有研究时间均具有显著的镇痛作用(p < 0.05)。提取物600 mg/kg时效果最佳。结果显示,提取物(600 mg/kg)在疼痛第二阶段的镇痛效果小于阿司匹林(300 mg/kg),在疼痛两个阶段的镇痛效果均小于吗啡(2.5 mg/kg),但在疼痛第一阶段大于阿司匹林。一组动物用纳洛酮(1 mg/kg,腹腔注射)和合适剂量的提取物(600 mg/kg,腹腔注射)进行处理。此外,纳洛酮抑制了奥利维香科叶草醇提取物的镇痛作用。可以得出结论,奥利维香科叶草醇提取物可能通过阿片受体发挥作用,刺激GABA能系统或促进内源性阿片肽的释放或减少自由基。