Antiviral and Cytotoxic Evaluation of Coumarins From Prangos Ferulacea Publisher Pubmed



Shokoohinia Y^{1, 2} ; Sajjadi SE³ ; Gholamzadeh S⁴ ; Fattahi A^{1, 5} ; Behbahani M⁶ Show Affiliations
Source: Pharmaceutical Biology Published:2014

Abstract

Context: Prangos ferulacea (L.) Lindl. (Apiaceae) is a perennial plant found in the Middle-East, where it is commonly used as an antispasmodic and anti-inflammatory agent. It is a rich source of coumarins. Objective: To purify several coumarins from P. ferulacea and to screen their cytotoxicity and anti-herpes activity. Materials and methods: Acetone extract of roots of P. ferulacea was subjected to several chromatographic separations to render pure coumarins (1-8). Anti-herpes virus effects of 1-7 were evaluated at concentration 2.5, 5, and 10gmL-1, on a confluent monolayer of Vero cells infected with 25 PFU of HSV1. Cytotoxic effects of 1 and 2 were evaluated on an A2780S cell line using the MTT assay. The cells were exposed to a series of concentrations of coumarins (0.01-2.5mM, 37°C, 72h). Results: Compounds 1-8 were identified as osthole, isoimperatorin, oxypeucedanin, psoralen, oxypeucedanin hydrate, gosferol, oxypeucedanin methnolate, and pranferol. This is the first report of occurrence of 4 and 7 in this plant. Compound 1 showed a viability of 9.41%±2.4 at 2.5mM on A2780S cells (IC50=0.38mM). The cell survival of 2 at 2.5mM was 46.86%±5.5 with IC50 equal to 1.1mM. Discussion and conclusion: Compound 1 shows cytotoxic effects on the A2780S cell line. Compound 2 is a cyclooxygenase-2 inhibitor and the A2780S cell line does not express COX-2 which may interpret the non-toxic effect of the compound on this cell line. None of the tested compounds showed an anti-HSV effect at non-toxic concentrations. © 2014 Informa Healthcare USA, Inc. All rights reserved: reproduction in whole or part not permitted.