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Quantification of Antinociceptive and Antiinflammatory Potentials of Different Ocimum gratissimum Linn. Leaf Extracts in Male Whistar Albino Rats

机译:定量的不同的免费Ocimum grasimsimum Linn的抗伤害感受和抗炎潜力的量化。雄性Whistar白化病大鼠的叶提取物

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Aim: This study was aimed at quantifying the antinociceptive and anti-inflammatory potency and efficacy of aqueous (AQ) and ethanolic leaf extracts of O. gratissimum (ET) in Whistar rats. Methodology: Inflammation (paw edema) was induced in rats (n=5 per group) with fresh egg albumin (0.1 ml); groups for anti-inflammatory experiment were pretreated (0.5 h), while those for anti-nociceptive experiment were post-treated (2.5 h) with AQ (200, 400 or 800 mg/kg, p.o.), ET (200, 400 or 800 mg/kg, p.o.), piroxicam (20 mg/kg, i.p.), or normal saline (1 mL/kg, i.p.). Paw sizes of anti-inflammatory group rats were measured at 0 and 2 h after injection of phlogistic agent using plethysmometer, whereas mechanical nociceptive thresholds were measured in anti-nociceptive group rats before and 2 h after test agent treatments using analgesymeter. Results: There was neither change in inflammatory reaction (after egg albumin injection at time 0 or 2 h) nor threshold in control rats before or after normal saline treatment. AQ inhibited ( P = .05) paw edema at 400 mg/kg (26%) and 800 mg/kg (64%); whereas all three doses of ET caused inhibitions (35, 39 and 32%, respectively) compared to the egg albumin induced values. AQ and ET treatments increased ( P = .05) mechanical nociceptive thresholds, but maximum effects were observed at 400 mg/kg for both extracts (144 and 270%, respectively) compared to values obtained before extract treatment. Piroxicam produced significant inhibitions in inflammation (20%) and nociception (100%). Conclusion: ET is more potent, but AQ is about twice as efficacious as ET in anti-inflammatory activity. Also, ET is more potent and has a higher analgesic efficacy than AQ.
机译:目的:本研究旨在定量评估Whistar大鼠中O. gratissimum(ET)的水(AQ)和乙醇叶提取物的抗伤害感受和抗炎作用以及功效。方法:用新鲜鸡蛋清蛋白(0.1 ml)诱导大鼠发炎(爪水肿)(每组n = 5);抗炎实验组进行了0.5小时的预处理,而抗伤害性实验组则进行了AQ(200、400或800 mg / kg,口服),ET(200、400或800)后处理(2.5 h)毫克/千克,口服),吡罗昔康(20毫克/千克,腹腔注射)或生理盐水(1毫升/千克,腹腔注射)。抗炎组大鼠的足爪大小在注射消炎剂后0和2小时使用体积描记器进行测量,而抗伤害感受性组大鼠在使用止痛剂治疗之前和之后2小时测量机械伤害感受性阈值。结果:正常生理盐水治疗前后,对照组大鼠的炎症反应(注射卵清蛋白在0或2 h后)均没有变化,也没有阈值。在400 mg / kg(26%)和800 mg / kg(64%)时,AQ抑制(P = .05)爪水肿;而与鸡蛋清蛋白诱导值相比,三剂ET均引起抑制(分别为35%,39%和32%)。 AQ和ET处理提高了机械伤害阈值(P = .05),但是与提取物处理之前获得的值相比,两种提取物在400 mg / kg时均观察到最大效果(分别为144%和270%)。吡罗昔康对炎症(20%)和伤害感受(100%)产生显着抑制作用。结论:ET更有效,但AQ的抗炎活性约为ET的两倍。而且,ET比AQ更有效并且具有更高的止痛效果。

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