W. Belem-Kabré, B. Kaboré, Adjaratou Compaoré-Coulibaly, Tata Kadiatou Traoré, Emmanuel A. M. Thiombiano, Mariam Nebié-Traoré, Moussa, Compaoré, F. Kini, S. Ouédraogo, M. Kiendrebeogo, N. Ouedraogo
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引用次数: 4
摘要
和番木瓜Carica papaya L.(加勒比科)是两种用于治疗几种人类疾病如氧化应激和炎症性疾病的植物。本研究旨在通过适当的实验模型,研究金针菇和木瓜的水提液和甲醇提液的抗炎活性、抗氧化活性和急性口服毒性。采用经济合作与发展(OECD)指南423对小鼠急性口服毒性试验进行评价。体外实验考察其对15-脂氧合酶、磷脂酶a2、环氧合酶1和环氧合酶2等关键炎症酶的抑制能力。采用四种方法(抑制脂质过氧化、FRAP、DPPH和ABTS试验)评估其体外抗氧化活性。植物化学筛选结果显示其含有甾醇、三萜、皂苷、黄酮类化合物、酚类物质和单宁。醇提物的酚类、缩合单宁、水解单宁和类黄酮含量分别为855.06±1.71 mg GAE/ g、418.22±1.92 mg CE / g、19.31±0.6 mg GAE/ g和20.6±0.36 mg QE / g。该提取物具有抗氧化能力,抑制促炎酶的潜力,致死剂量(ld50)估计为5000 mg/kg b.w。该研究结果为证明这些植物的传统用途提供了坚实的科学依据。
Phytochemical and biological investigations of extracts from the roots of Cocos nucifera L. (Arecaceae) and Carica papaya L. (Caricaceae), two plants used in traditional medicine
and Carica papaya L. (Caricaceae) are two plants used to treat several human pathologies such as oxidative stress and inflammatory diseases. The aim of this study is to assess anti-inflammatory activity, antioxidant activity and acute oral toxicity, of aqueous and methanolic extracts from C. nucifera L. and C. papaya L. using appropriate experimental models. The acute oral toxicity test of extracts on mice was evaluated using Economic Cooperation and Development (OECD) guidelines 423. The capacity of extracts to inhibit key inflammation enzymes such as 15-lipoxygenase, phospholipase A 2 , cyclooxygenases 1 and 2 was evaluated in vitro . The antioxidant activity was assessed in vitro using four methods (inhibition of lipid peroxidation, FRAP, DPPH and ABTS tests). The phytochemical screening showed the presence of sterols and triterpenes, saponins, flavonoids, phenolics and tannins. Methanolic extract from C. nucifera exhibited higher values of 855.06 ± 1.71 mg GAE/ g, 418.22 ± 1.92 mg CE / g, 19.31 ± 0.6 mg GAE / g, 20.6 ± 0.36 mg QE / g dry extract respectively for phenolics, condensed tannins, hydrolysable tannins and flavonoid content. The extracts demonstrated antioxidant capacity, potential to inhibit pro-inflammatory enzymes and a lethal dose (LD 50 ) was estimated to 5000 mg/kg b.w. The results of this study constitute a solid scientific basis that can justify the traditional uses of these plants.