Leishmanicidal activity of polysaccharides and their oxovanadium(IV/V) complexes
- PMID: 25506811
- DOI: 10.1016/j.ejmech.2014.12.003
Leishmanicidal activity of polysaccharides and their oxovanadium(IV/V) complexes
Abstract
The parasites of the genus Leishmania cause a range of leishmaniasis diseases, whose treatment is impaired due to intramacrophage parasites living in the mammalian host. Immunostimulation has been considered an important strategy to leishmaniasis treatment. The immunomodulatory effects of the polysaccharides arabinogalactan (ARAGAL), galactomannan (GMPOLY), and xyloglucan (XGJ), as well as their oxovanadium (IV/V) complexes (ARAGAL:VO, GMPOLY:VO, and XGJ:VO) were evaluated on peritoneal macrophages. At 25 μg/mL of GMPOLY:VO and of XGJ:VO, and 10 μg/mL of ARAGAL:VO, nitric oxide (NO) production by the macrophages was not altered compared with the control group. All polymers increased the production of interleukins 1 beta and 6 (IL-1β and IL-6), but the oxovanadium complexes were more potent activators of these mediators. ARAGAL:VO 10 μg/mL, GMPOLY:VO and XGJ:VO 25 μg/mL led to an increase of 562%, 1054%, and 523% for IL-1β, respectively. For IL-6 at the same concentration, the levels increased by 539% and 794% for ARAGAL:VO and GMPOLY:VO, respectively. Polysaccharides and their oxovanadium complexes exhibited important leishmanicidal effects on amastigotes of Leishmania (L.) amazonensis. The native and complexed polymers reduced the growth of promastigote-form Leishmania by ∼60%. This effect was reached at concentrations 12 times lower than that observed for Glucantime (300 μg/mL promoted an inhibition of ∼60%). The 50% inhibitory concentration (IC50) values for the complexes were determined. XGJ:VO showed the lowest IC50 value (6.2 μg/mL; 0.07 μg/mL of vanadium), which for ARAGAL:VO was 6.5 μg/mL (0.21 μg/mL of vanadium) and 7.3 μg/mL (0.06 μg/mL of vanadium) for GMPOLY:VO. The upregulation of IL-1β and IL-6 release and downregulation of NO production by macrophages and the important leishmanicidal effect are essential to stablish their potential use against this pathology.
Keywords: Immunomodulators; Leishmaniasis; Oxovanadium(IV/V) complexes; Polysaccharides.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.
Similar articles
-
Macrophage activation and leishmanicidal activity by galactomannan and its oxovanadium (IV/V) complex in vitro.J Inorg Biochem. 2014 Mar;132:45-51. doi: 10.1016/j.jinorgbio.2013.09.017. Epub 2013 Oct 9. J Inorg Biochem. 2014. PMID: 24169303
-
Effects of a lichen galactomannan and its vanadyl (IV) complex on peritoneal macrophages and leishmanicidal activity.Mol Cell Biochem. 2002 Apr;233(1-2):73-83. doi: 10.1023/a:1015566312032. Mol Cell Biochem. 2002. PMID: 12083382
-
Acid heteropolysaccharides with potent antileishmanial effects.Int J Biol Macromol. 2015 Nov;81:165-70. doi: 10.1016/j.ijbiomac.2015.07.006. Epub 2015 Jul 7. Int J Biol Macromol. 2015. PMID: 26162246
-
A comprehensive review of chalcone derivatives as antileishmanial agents.Eur J Med Chem. 2018 Apr 25;150:920-929. doi: 10.1016/j.ejmech.2018.03.047. Epub 2018 Mar 22. Eur J Med Chem. 2018. PMID: 29602038 Review.
-
A "Golden Age" for the discovery of new antileishmanial agents: Current status of leishmanicidal gold complexes and prospective targets beyond the trypanothione system.ChemMedChem. 2021 Jun 7;16(11):1681-1695. doi: 10.1002/cmdc.202100022. Epub 2021 Mar 22. ChemMedChem. 2021. PMID: 33615725 Review.
Cited by
-
Hypoxia protects against the cell death triggered by oxovanadium-galactomannan complexes in HepG2 cells.Cell Mol Biol Lett. 2019 Mar 22;24:18. doi: 10.1186/s11658-019-0135-3. eCollection 2019. Cell Mol Biol Lett. 2019. PMID: 30949212 Free PMC article.
-
Nanostructured delivery systems with improved leishmanicidal activity: a critical review.Int J Nanomedicine. 2017 Jul 26;12:5289-5311. doi: 10.2147/IJN.S140363. eCollection 2017. Int J Nanomedicine. 2017. PMID: 28794624 Free PMC article. Review.
-
Sources, Extraction and Biomedical Properties of Polysaccharides.Foods. 2019 Aug 1;8(8):304. doi: 10.3390/foods8080304. Foods. 2019. PMID: 31374889 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical