In vitro antiplasmodial activity and identification, using tandem LC-MS, of alkaloids from Aspidosperma excelsum, a plant used to treat malaria in Amazonia

被引:7
作者
do Nascimento, Myrth Soares [1 ]
Vieira Pina, Nayla di Paula [1 ]
Brigida da Silva, Andressa Santa [1 ]
dos Santos Gomes, Luis Fabio [1 ]
de Vasconcellos, Flavio [1 ]
Brandao, Geraldo Celio [2 ]
Alves do Nascimento, Maria Fernanda [3 ]
de Oliveira, Alaide Braga [3 ]
Ramos Barbosa, Wagner Luiz [1 ,4 ]
机构
[1] Fed Univ Para, Grad Program Pharmaceut Sci, R Augusto Correa 01, BR-66075110 Belem, Para, Brazil
[2] Univ Fed Ouro Preto, Fac Pharm, R Diogo Vasconcelos 122, BR-35400000 Ouro Preto, MG, Brazil
[3] Univ Fed Minas Gerais, Fac Pharm, Av Antonio Carlos 6627, BR-31270901 Belo Horizonte, MG, Brazil
[4] Fed Univ Para, Inst Hlth Sci, Fac Pharm, R Augusto Correa 01, BR-66075110 Belem, Para, Brazil
关键词
Apocynaceae; Anti-malarial activity; Plasmodium falciparum; Indole-alkaloids; UPLC-ESI-MS/MS; HPLC-MS MicroTOF; ANTIMALARIAL ACTIVITY; INDOLE ALKALOIDS; MEDICINAL-PLANTS; PLASMODIUM-FALCIPARUM; APOCYNACEAE; CYTOTOXICITY;
D O I
10.1016/j.jep.2018.09.012
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Aspidosperma excelsum Benth. (Apocynaceae), a native tree in the Brazilian Amazonia, is traditionally used to treat various diseases, including malaria. Aim of study: To investigate the chemical constitution, antiplasmodial activity and cytotoxicity of samples obtained from A. excelsum trunk bark by different procedures aiming to evaluate their potential as an antimalarial phytomedicine. Materials and methods: A hydroethanolic extract and alkaloid extracts were prepared and assayed for antiplasmodial activity and cytotoxicity against chloroquine-resistant Plasmodium falciparum (W2 strain) and HepG2 cells, respectively. Taking into account the known occurrence and antimalarial activity of Aspidosperma monoterpene indole alkaloids (MIA), acid-base extractions were carried out and the fractions were assayed for antiplasmodial activity and cytotoxicity. All the samples were analysed by hyphenated chromatographic techniques, such as UPLC-DAD-ESI-MS/MS and HRMS (HPLC-MS MicroTOF), comparing their chemical composition to the literature data. Results: The hydroethanolic extract disclosed a moderate in vitro activity against chloroquine-resistant Plasmodium falciparum (W2 strain) with IC50 23.68 +/- 3.08 mu g/mL), low cytotoxicity to HepG2 cells (> 250 mu g/mL) and good SI (> 10.56). A total of 20 known monoterpene indole alkaloids were identified, seven of which are here firstly described for A. excelsum. Known highly active alkaloids, namely demethylaspidospermine, aspidocarpine, and ochrolifuanine are present in active alkaloid fractions and might contribute to their observed antiplasmodial effect. An alkaloid fraction (Ae-Alk2), obtained directly from trunk bark by extraction with dil. aqueous HCl, pointed out for its activity (IC50 8.75 +/- 2.26 mu g/mL, CC50 185.14 +/- 1.97 mu g/mL, SI 21.16) and should be highlighted as the most promising out of the assayed samples. Conclusion: The present results represent a preliminary support to the alleged antimalarial use of A. excelsum trunk bark and allowed to highlight alkaloid fractions as promising phytomedicines.
引用
收藏
页码:99 / 109
页数:11
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