Study on the In Vivo Antimalarial Activity of Solvent Fractions of the Leaf of Vernonia Amygdalina (Asteraceae) against Plasmodium Berghei in Mice

Bihonegn, Temesgen (2016) Study on the In Vivo Antimalarial Activity of Solvent Fractions of the Leaf of Vernonia Amygdalina (Asteraceae) against Plasmodium Berghei in Mice. Masters thesis, Addis Ababa University.

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Abstract

Malaria is a mosquito borne infectious disease caused by a protozoan of the genus Plasmodium. Around 44% of world‟s population is at risk from malaria. Malaria is one of the leading causes of morbidity and mortality in Ethiopia. The most important problem associated with the management of malaria are resistant to or are developing resistance to the most widely available, affordable and safest first line treatments. The study was under taken to evaluate the in vivo antimalarial activity of solvent fractions of the leaves of Vernonia amygdalina against P. berghei infection in mice using four day suppressive test and subsequently body temperature, weight, packed cell volume, parasitemia and mean survival time were determined. The plant has been extracted using cold maceration. 80% methanol crude extract of V. amygdalina was subjected to chloroform, butanol and aqueous fraction. Tween 80 2% and distilled water as negative control and chloroquine 25 mg/kg were used as positive control. Acute oral toxicity test showed that both the aqueous and hydroalcolic extracts and solvent fractions of the leaves of Vernonia amygdalina revealed no mortality and signs of toxicities up to 2000mg/kg. The present study indicated that the percentage suppression of hydroalcoholic extract was 32.47%, 35.4% and 37.67% at 200, 400 and 600mg/kg of the extract, respectively and the percentage suppression of aqueous extract was 21.22%, 22.20% and 24.52% at 200 400 and 600mgmkg of the extract respectively. All doses of crude extracts of V. amygdalina prolonged the survival time, shown prevention against weight loss and prevent PCV reduction in a dose dependent manner. Except aqueous fraction, all doses of chloroform and butanol fractions were suppressed parasitemia significantly. The percentage suppression of chloroform fraction was 21.68%, 23.72% and 33.85 % at 100, 200 and400mg/kg of the fraction, respectively. The 100 and 200 mg/kg of butanol fraction resulted in moderate anti-plasmodial activity (18.12%, and 21.03% %, respectively), followed by the 400 mg/kg (26.88%).The mean survival effects of both chloroform and butanol fractions were capable of significantly increasing survival time at all doses compared to negative control. All the tested doses of chloroform and butanol fractions exhibited reduction in rectal temperature of Plasmodium berghei infected mice statistically significant (p <0.05) in a dose-dependent manner. All doses of chloroform, butanol and aqueous fractions had shown prevention against weight loss (p<0.001). The results of the present study indicated that the in vivo administration of both extracts and solvent fractions of the leaf of V. amygdalina possess antimalarial activity and were capable of suppressing parasitemia. This confirms their use in ethnomedicine in the treatment of malaria in local communities. Therefore, there is a need to advance the current status of Vernonia amygdalina to an antimalarial lead drug level through isolation and characterization active antiplasmodial components in the extracts and solvent fractions. Further studies should carried out to determine the mechanism of action(s) responsible for the antimalarial activities.

Item Type: Thesis (Masters)
Uncontrolled Keywords: Antimalarial activity, Four day suppressive test, In vivo, P.berghei, Solvent fractions, Mice, V. amygdalina
Subjects: R Medicine > RA Public aspects of medicine > RA0421 Public health. Hygiene. Preventive Medicine
R Medicine > RM Therapeutics. Pharmacology
R Medicine > RS Pharmacy and materia medica
Divisions: Africana
Depositing User: Emmanuel Ndorimana
Date Deposited: 26 Jul 2018 07:23
Last Modified: 26 Jul 2018 07:23
URI: http://thesisbank.jhia.ac.ke/id/eprint/8169

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