Abstract

ObjectiveThe aim of this study was to investigate the antiplasmodial effects of the crude aqueous, methanol and chloroform extracts of the leaves of Vernonia adoensis in Plasmodium berghei infected Swiss albino mice using Peters’ 4-day suppressive test.ResultsThe number of mice used for the toxicity test was 20 (5/group) and for each extract and control groups 5 mice per group was used. The aqueous, methanol and chloroform extracts of V. adoensis leaves indicated statistically significant (P < 0.05) suppression of parasitaemia in the treated mice. The highest inhibition was that of the methanol extract treated mice (83.36%) followed by aqueous (72.26%) and chloroform (54.34%) at an oral dose of 600 mg/kg b.wt. Each extract prevented body weight loss and packed cell volume (PCV) reduction as compared to the negative control groups. The survival time of the mice treated with chloroform based on Kaplan–Meir analysis was 12.53 ± 0.37 at 600 mg/kg b.wt, while the negative control was 7.93 ± 0.37 days. The LD50 of the extracts was greater than 3000 mg/kg body weight. In conclusion, the crude leaves extract of V. adoensis have demonstrated antiplasmodial effect in vivo. P. berghei infection is suppressed in a dose-dependent manner showing relevance of the traditional use of the plant.

Highlights

  • Malaria is still a public health problem in many parts of the tropics

  • Antiplasmodial activity The results of this study indicated that the in vivo aqueous, methanol and chloroform leaf extracts of V. adoensis exhibited a potent activity against P. berghei malaria parasite (Table 1)

  • The Parasitaemia suppressive effects produced by all the test extracts were significant (P < 0.05) as compared with their respective negative control groups

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Summary

Results

Toxicity test No death occurred in any of the groups and dose levels during the entire period of 24 h of observation. The Parasitaemia suppressive effects produced by all the test extracts were significant (P < 0.05) as compared with their respective negative control groups. Each result showed that PCV in the respective negative control groups were significantly (P < 0.05) reduced in D­ 4 while in the extracts treated groups significant change was not observed (P > 0.05). Mean survival time All the experimental mice treated with the different extracts had increased dose dependent mean survival days (e.g. the chloroform extract exhibited the maximum MST of 12.53 at 600 mg/kg b.wt) as compared to the respective negative control groups (the maximum MST was 7.93). All the mice treated with CQ survived for 3 months (Additional file 1)

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