Phytochemical characterization, Antioxidant and Analgesic potentials of Aerial Parts of Eruca vesicaria

S. Halmi, Madi Aicha, Cherfia Radia, Zeghad Nadia, Beroual Katiba
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Abstract

Our work is based on the phytochemical study, the antioxidant and the analgesic activities of a hydroalcoholic extract of Eruca vesicaria aerial part very used in traditional medicine. The phytochemical screening highlighted the presence of tannins, flavonoids, sterols, flavonoid glucosides, saponins, phenols and alkaloids. The determination of total phenols of hydromethanolic extract by the Folin-ciocalteu method revealed a content equal to 4.63 ± 0.017 mg GAE / g extract. The amount of flavonoids by AlCl3 method achieved a content equal to 2.14 ± 0.025 mg QE/ g extract. The antiradical activities were evaluated by two chemical tests ; DPPH and FRAP. The obtained results showed a high reducing activity. Besides, the acute toxicity and the analgesic activity of the plant extract was evaluated on rats, using a pain model induced by chemical stimuli, hot plate and tail immersion methods. The extract was used at various doses 100, 200 and 300 mg/kg, whereas acetylsalicylic acid was used as the standard drug (200 mg/kg). In the acetic acid-induced model, the plant extracts and the standard drug significantly (p<0.05) reduced the abdominal writhing in rats compared to the control group by increasing the percentage of writhing inhibition in a dose-dependent manner. In the hot plate and the tail immersion models, the plant extracts and the standard drug acetylsalicylic acid demonstrated a good analgesic activity and significantly (p<0.05) increasing the pain reaction time. These results indicate that the E. vesicaria plant has a significant analgesic potential that can act through peripheral and central mechanisms.
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云杉地上部位的植物化学性质、抗氧化和镇痛作用
本研究是基于对传统医学常用部位的水醇提取物的植物化学、抗氧化和镇痛活性的研究。植物化学筛选突出了单宁、类黄酮、甾醇、类黄酮苷、皂苷、酚类和生物碱的存在。采用Folin-ciocalteu法测定水甲醇提取物总酚含量为4.63±0.017 mg GAE / g提取物。AlCl3法提取的黄酮含量为2.14±0.025 mg QE/ g提取物。通过两种化学试验对其抗自由基活性进行了评价;DPPH和FRAP。所得结果显示出较高的还原活性。采用化学刺激、热板法和尾浸法建立大鼠疼痛模型,评价其急性毒性和镇痛活性。以乙酰水杨酸为标准药(200 mg/kg),以100、200和300 mg/kg的不同剂量使用提取物。在乙酸诱导模型中,植物提取物和标准药物通过增加扭体抑制率,显著降低大鼠腹部扭体,且呈剂量依赖性(p<0.05)。在热板和尾浸泡模型中,植物提取物和标准药物乙酰水杨酸均表现出良好的镇痛活性,并显著(p<0.05)延长了疼痛反应时间。这些结果表明,荆芥具有明显的镇痛潜能,可通过外周和中枢机制发挥作用。
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