Antiplasmodial Activities of Flavonoids from Leaves of Securidaca longepedunculata Fresen (Polygalaceae)

Issa Karama, M. Compaoré, Abdoulaye Djandé, Orokia Traoré, L. Lagnika, M. Kiendrebeogo
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引用次数: 2

Abstract

The discovery of new molecules for fighting against malaria is still relevant to overcome Plasmodium sp resistance. Phenolic compounds from medicinal plants have shown antiplasmodial properties. In addition, the targets of flavonoids on P. falciparum are multiple. This work aimed to identify the antiplasmodial compounds from methanol extract of Securidaca longepedunculata leaves. The inhibition of β-hematin formation was used to detect antiplasmodial compounds through a bio-guided chromatographic fractionation procedures. W2 strain was inhibited by flavonoids fractions Fc1 and Fb4 with 6.98 and 10.39 µg/mL as IC50 respectively. Also, fractions of phenol acids have shown good activities on the inhibition of β-hematin formation. The HPLC analyze showed that S. longepedunculata leaves extract contained quercetin, 3-β-quercetin, luteolin, chrysin, isorhamnetin, hyperoside, rutin, gallic acid, ellagic acid, chlorogenic acid, tannic acid and ferulic acid. Among these compounds identified, some had shown antiplasmodial and inhibitory activities on the formation of β-hematin. The antimalarial activity of the leaves of S. longepedunculata would be due in part to phenolic acids and flavonoids. The antiplasmodial activity observed in this work would be due in part to the ability of flavonoids from S. longepedunculata leaves to inhibit the formation of β-hematin. This finding could justify partially the S. longepedunculata uses in malaria treatment in Burkina Faso.
长柄松叶黄酮类化合物的抗疟原虫活性研究
抗击疟疾的新分子的发现对克服疟原虫的耐药性仍然具有重要意义。药用植物中的酚类化合物具有抗疟原虫的特性。此外,黄酮类化合物对恶性疟原虫的作用靶点是多种多样的。本研究旨在鉴定长柄松柏叶甲醇提取物中的抗疟原虫化合物。抑制β-血红素形成被用于检测抗疟原虫化合物通过生物引导色谱分离程序。黄酮类化合物Fc1和Fb4对W2菌株的IC50分别为6.98和10.39µg/mL。此外,苯酚酸的组分也显示出良好的抑制β-血红素形成的活性。HPLC分析表明,长柄山楂叶提取物中含有槲皮素、3-β-槲皮素、木犀草素、菊花素、异鼠李素、金丝桃苷、芦丁、没食子酸、鞣花酸、绿原酸、单宁酸和阿魏酸。在这些已鉴定的化合物中,一些已显示出抗疟原虫和抑制β-血红素形成的活性。长柄参叶的抗疟活性可能与酚酸和黄酮类化合物有关。本研究中观察到的抗疟原虫活性部分是由于长柄参叶中的黄酮类化合物能够抑制β-血红素的形成。这一发现可以在一定程度上证明在布基纳法索使用长柄棘球绦虫治疗疟疾是合理的。
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