Anti-Toxoplasma activity of Sorghum bicolor-derived lipophilic fractions.

BMC Res Notes

Department of Pathobiology, College of Veterinary Medicine, University of Illinois, Urbana-Champaign, IL, 61802, USA.

Published: October 2019

AI Article Synopsis

  • Toxoplasma gondii infects about a third of the global population, and existing treatments have limitations like ineffectiveness and side effects, highlighting the need for new drugs.
  • Research tested oil-like crude extracts from Sorghum bicolor, traditionally used in Africa for treating infections, for their anti-Toxoplasma activity.
  • The study found that these extracts significantly inhibited T. gondii growth with minimal toxicity to human cells, suggesting potential for developing new treatments or nutraceuticals.

Article Abstract

Objective: Toxoplasma gondii, an intracellular zoonotic parasite, infects approximately a third of the world population. Current drugs for treatment of T. gondii infection have been challenged with ineffectiveness and adverse side effects. This necessitates development of new anti-Toxoplasma drugs. Sorghum bicolor [Moench] leaf extract has been used in African traditional medicine for the management of anemia and treatment of infectious diseases. We tested the in vitro anti-Toxoplasma inhibitory activity of S. bicolor's oil-like crude extracts and fractions against T. gondii and determined their cytotoxic effects on human host cells.

Results: Significant inhibitory activities against the growth of T. gondii tachyzoites were observed for the crude extract (IC = 3.65 µg/mL), the hexane-methanol fraction (IC = 2.74 µg/mL), and the hexane fraction (IC50 = 3.55 µg/mL) after 48 h of culture. The minimum cytotoxicity concentrations against HFF were 34.41, 16.92 and 7.23 µg/mL for crude extract, hexane-methanol and hexane fractions, respectively. The crude extract and fractions showed high antiparasitic effects with low cytotoxic effects. Further studies to determine synergistic activities and modes of action would provide impetus for the development of new toxoplasmosis drugs or nutraceuticals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814109PMC
http://dx.doi.org/10.1186/s13104-019-4732-zDOI Listing

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