da Costa-Silva Thais Alves, Grecco Simone S, de Sousa Fernanda S, Lago João Henrique G, Martins Euder G A, Terrazas César A, Varikuti Sanjay, Owens Katherine L, Beverley Stephen M, Satoskar Abhay R, Tempone Andre G
†Center for Parasitology and Mycology, Instituto Adolfo Lutz, São Paulo, Brazil.
‡Center of Natural Sciences and Humanities, Federal University of ABC, São Paulo, Brazil.
J Nat Prod. 2015 Apr 24;78(4):653-7. doi: 10.1021/np500809a. Epub 2015 Apr 2.
Three phenylpropanoid dimers (1-3) including two new metabolites were isolated from the extract of the twigs of Nectandra leucantha using antileishmanial bioassay-guided fractionation. The in vitro antiparasitic activity of the isolated compounds against Leishmania donovani parasites and mammalian cytotoxicity and immunomodulatory effects were evaluated. Compounds 1-3 were effective against the intracellular amastigotes within macrophages, with IC50 values of 26.7, 17.8, and 101.9 μM, respectively. The mammalian cytotoxicity, given by the 50% cytotoxic concentration (CC50), was evaluated against peritoneal macrophages. Compounds 1 and 3 were not toxic up to 290 μM, whereas compound 2 demonstrated a CC50 value of 111.2 μM. Compounds 1-3 also suppressed production of disease exacerbatory cytokines IL-6 and IL-10 but had minimal effect on nitric oxide production in L. donovani-infected macrophages, indicating that antileishmanial activity of these compounds is mediated via an NO-independent mechanism. Therefore, these new natural products could represent promising scaffolds for drug design studies for leishmaniasis.
采用抗利什曼原虫生物测定导向分馏法,从白楠细枝提取物中分离出三种苯丙素二聚体(1-3),其中包括两种新的代谢产物。评估了分离出的化合物对杜氏利什曼原虫的体外抗寄生虫活性以及对哺乳动物的细胞毒性和免疫调节作用。化合物1-3对巨噬细胞内的无鞭毛体有效,IC50值分别为26.7、17.8和101.9μM。通过50%细胞毒性浓度(CC50)评估了对腹膜巨噬细胞的哺乳动物细胞毒性。化合物1和3在高达290μM时无毒,而化合物2的CC50值为111.2μM。化合物1-3还抑制了疾病加重细胞因子IL-6和IL-10的产生,但对杜氏利什曼原虫感染的巨噬细胞中一氧化氮的产生影响最小,表明这些化合物的抗利什曼原虫活性是通过非一氧化氮依赖机制介导的。因此,这些新的天然产物可能是利什曼病药物设计研究的有前景的支架。