Benzoic acid derivatives of Ifloga spicata (Forssk.) Sch.Bip. as potential anti-leishmanial against Leishmania tropica

• Main Authors: Ayaz, M. (Author), Hussain, S. (Author), Nadhman, A. (Author), Sadiq, A. (Author), Shah, A.-H.A (Author), Shah, S.A.A (Author), Shah, S.M (Author), Ullah, F. (Author), Ullah, I. (Author), Ullah, N. (Author)
• Format: Article
• Language: English
• Published: MDPI AG 2019
• Subjects: Apoptosis; Benzoic acid derivatives; DNA interaction; Docking; Ifloga spicata; Leishmania tropica
• Online Access: View Fulltext in Publisher; View in Scopus
• ISBN: 22279717 (ISSN)
• ISSN: 22279717 (ISSN)
• DOI: 10.3390/pr7040208

This study aimed to appraise the anti-leishmanial potentials of benzoic acid derivatives, including methyl 3,4-dihydroxybenzoate (compound 1) and octadecyl benzoate (compound 2), isolated from the ethnomedicinally important plant Ifloga spicata (I. spicata). Chemical structures were elucidated via FT-IR, mass spectrometry, and multinuclear (1H and 13C) NMR spectroscopy. Anti-leishmanial potentials of the compounds were assessed using Leishmania tropica promastigotes. Moreover, acridine orange fluorescent staining was performed to visualize the apoptosis-associated changes in promastigotes under a fluorescent microscope. A SYTOX assay was used to check rupturing of Leishmania promastigote cell membranes using 0.1% Triton X-100 as positive control. A DNA interaction assay was carried out to assess DNA attachment potential. AutoDock software was used to check the binding affinity of compounds with surface enzyme leishmanolysin gp63 (1LML). Both compounds exhibited considerable anti-leishmanial potential, with LD50 values of 10.40 ± 0.09 and 14.11 ± 0.11 μg/mL for compound 1 and compound 2, respectively. Both compounds showed higher binding affinity with the leishmanolysin (gp63) receptor/protease of Leishmania, as assessed using computational analysis. The binding scores of compounds 1 and 2 with target gp63 were -5.3 and -5.6, respectively. The attachment of compounds with this receptor resulted in their entry into the cell where they bound with Leishmania DNA, causing apoptosis. The results confirmed that the investigated compounds have anti-leishmanial potential and are potential substitutes as natural anti-leishmanial agents against L. tropica. © 2019 by the authors.