Immunomodulatory and Antileishmanial Activity of Phenylpropanoid Dimers Isolated from Nectandra leucantha

被引:54
作者
da Costa-Silva, Thais Alves [1 ]
Grecco, Simone S. [2 ]
de Sousa, Fernanda S. [3 ]
Lago, Joao Henrique G. [3 ]
Martins, Euder G. A. [4 ]
Terrazas, Cesar A. [5 ,6 ]
Varikuti, Sanjay [5 ,6 ]
Owens, Katherine L. [7 ]
Beverley, Stephen M. [7 ]
Satoskar, Abhay R. [5 ,6 ]
Tempone, Andre G. [1 ]
机构
[1] Adolfo Lutz Inst, Ctr Parasitol & Mycol, Sao Paulo, Brazil
[2] Fed Univ ABC, Ctr Nat Sci & Humanities, Sao Paulo, Brazil
[3] Univ Fed Sao Paulo, Inst Environm Chem & Pharmaceut Sci, Sao Paulo, Brazil
[4] Univ Sao Paulo, Dept Bot, Inst Biosci, Sao Paulo, Brazil
[5] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[6] Ohio State Univ, Dept Microbiol, Columbus, OH 43210 USA
[7] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2015年 / 78卷 / 04期
基金
巴西圣保罗研究基金会;
关键词
NITRIC-OXIDE; VISCERAL LEISHMANIASIS; CONSTITUENTS; MILTEFOSINE; EXTRACTS; FAILURE; LIGNANS; ASSAY;
D O I
10.1021/np500809a
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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 mu M, 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 mu M, whereas compound 2 demonstrated a CC50 value of 111.2 mu M. 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.
引用
收藏
页码:653 / 657
页数:5
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