In vitro antiviral activity of piperidine alkaloids from Senna spectabilis flowers on Chikungunya virus infection

被引:9
作者
Freitas, Thamires Rodrigues [1 ]
Novais, Raul Marques [1 ]
Santos, Igor Andrade [2 ]
Silva Martins, Daniel Oliveira [2 ,3 ]
Danuello, Amanda [1 ]
Bolzani, Vanderlan da Silva [4 ]
Gomes Jardim, Ana Carolina [2 ,3 ]
Pivatto, Marcos [1 ]
机构
[1] Univ Fed Uberlandia, Inst Quim, Nucleo Pesquisa Compostos Bioativos NPCBio, BR-38400902 Uberlandia, MG, Brazil
[2] Univ Fed Uberlandia, Inst Ciencias Biomed ICBIM, Lab Pesquisa Antivirais, BR-38405317 Uberlandia, MG, Brazil
[3] Univ Estadual Paulista, BR-15054000 Sao Jose Do Rio Preto, SP, Brazil
[4] Univ Estadual Paulista, Inst Quim, Dept Quim Organ, Nucleo Bioensaios Biossintese & Ecofisiol Prod Na, POB 355, BR-14801970 Araraquara, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Senna spectabilis; Fabaceae; Piperidine alkaloids; Neglected tropical diseases; Chikungunya fever; Chikungunya virus; Antiviral; MEDICINAL CHEMISTRY; EXTRACTS;
D O I
10.1007/s43440-022-00381-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Chikungunya fever is an endemic disease caused by the Chikungunya virus (CHIKV). To date there is no antiviral treatment against this infection or licensed vaccine to prevent it. Our study aims to evaluate whether (-)-cassine (1) and (-)-spectaline (2), the main alkaloids of Senna spectabilis, display anti-CHIKV activity. Both compounds have been described to be biologically active against neglected tropical diseases, including malaria, leishmaniasis, and schistosomiasis, which emphasizes that these molecules could be repurposed for chikungunya fever treatment. Methods The structures of the isolated compounds 1 and 2 were identified by NMR and HRESIMS analyses, and their antiviral activity against CHIKV was assessed by a dose-response assay employing BHK-21 cells and CHIKV-nanoluc, a recombinant virus carrying the nanoluciferase gene reporter. Results Compound 1 presented CC50 of 126.5 mu M and EC50 of 14.9 mu M, while compound 2 presented CC50 of 91.9 mu M and EC50 of 8.3 mu M. The calculated selectivity index (SI) was 8.5 for 1 and 11.3 for 2. Conclusion The data presented herein show that compounds 1 and 2 have potential for being repurposed as anti-CHIKV drug. Our promising in vitro results encourage further in vitro and in vivo assays. This is the first description of the antiviral activity of compounds 1 and 2 against CHIKV infection, which can impact the development of antiviral drug candidates against chikungunya fever, which sometimes can be debilitating.
引用
收藏
页码:752 / 758
页数:7
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