Neolignans isolated from Saururus cernuus L. (Saururaceae) exhibit efficacy against Schistosoma mansoni

被引:17
作者
Brito, Juliana R. [1 ]
Wilairatana, Polrat [2 ]
Roquini, Daniel B. [3 ]
Parra, Beatriz C. [3 ]
Goncalves, Marina M. [4 ]
Souza, Dalete Christine S. [4 ]
Ferreira, Edgard A. [5 ]
Salvadori, Maria C. [6 ]
Teixeira, Fernanda S. [6 ]
Lago, Joao Henrique G. [4 ]
de Moraes, Josue [3 ]
机构
[1] Univ Fed Sao Paulo, Inst Environm Chem & Pharmaceut Sci, BR-09972270 Diadema, SP, Brazil
[2] Mahidol Univ, Fac Trop Med, Dept Clin Trop Med, Bangkok 10400, Thailand
[3] Univ Guarulhos, Res Ctr Neglected Dis, BR-07023070 Guarulhos, SP, Brazil
[4] Fed Univ ABC, Ctr Nat & Human Sci, BR-09210180 Santo Andre, SP, Brazil
[5] Univ Prebiteriana Mackenzie, Sch Engn, BR-01302907 Sao Paulo, SP, Brazil
[6] Univ Sao Paulo, Inst Phys, BR-05508090 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
ANTISCHISTOSOMAL ACTIVITY; ANTIPARASITIC ACTIVITY; LIGNANS; DRUG; PRAZIQUANTEL; AGENTS; ANTIBACTERIAL; CYTOTOXICITY; MECHANISMS; PIPLARTINE;
D O I
10.1038/s41598-022-23110-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Schistosomiasis, a parasitic disease caused by the blood fluke of the genus Schistosoma, affects over 230 million people, especially in developing countries. Despite the significant economic and public health consequences, only one drug is currently available for treatment of schistosomiasis, praziquantel. Thus, there is an urgent demand for new anthelmintic agents. Based on our continuous studies involving the chemical prospection of floristic biodiversity aiming to discover new bioactive compounds, this work reports the in vitro antiparasitic activity against Schistosoma mansoni adult worms of neolignans threo-austrobailignan-6 and verrucosin, both isolated from Saururus cernuus L. (Saururaceae). These neolignans showed a significant in vitro schistosomicidal activity, with EC50 values of 12.6-28.1 mu M. Further analysis revealed a pronounced reduction in the number of S. mansoni eggs. Scanning electron microscopy analysis revealed morphological alterations when schistosomes were exposed to either threo-austrobailignan-6 or verrucosin. These relevant antischistosomal properties were accompanied by low cytotoxicity potential against the animal (Vero) and human (HaCaT) cell lines, resulting in a high selectivity index. Considering the promising chemical and biological properties of threo-austrobailignan-6 and verrucosin, this research should be of interest to those in the area of neglected diseases and in particular antischistosomal drug discovery.
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页数:12
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