Events7th International Electronic Conference on Medicinal Chemistry
Published
This submission belongs to the session S5. Round table on natural products of the event 7th International Electronic Conference on Medicinal Chemistry
Published date
03 Nov, 2021
Academic Editor
author-avatarJean Jacques Vanden Eynde
Citation
Innocent Uzochukwu Okagu, Victor N Ogugua, Bartholomew O. Okolo, Sunday N. Okafor, In vitro anti-plasmodial and in vivo malaria chemoprotective properties of methanol extract of Zanthoxylum zanthoxyloides root bark and its fractions, in Proceedings of 7th International Electronic Conference on Medicinal Chemistry, 1 November–30 November 2021, MDPI: Basel, Switzerland, doi: 10.3390/ECMC2021-11552
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In vitro anti-plasmodial and in vivo malaria chemoprotective properties of methanol extract of Zanthoxylum zanthoxyloides root bark and its fractions

Victor N Ogugua 2
1. Department of Biochemistry, University of Nigeria, Nsukka, Nigeria, Nigeria
2. Department of Biochemistry, Faculty of Biological Sciences, University of Nigeria, Nsukka, Enugu State, Nigeria.
3. Department of Pharmaceutical and Medicinal Chemistry, University of Nigeria, Nsukka, 410001, Enugu State, Nigeria
Abstract

Rural dwellers in Nigeria and other parts of West Africa use root barks of Zanthoxylum zanthoxyloides L. for treating sickle cell anaemia, cancers, fever and malaria. This study evaluated in vitro anti-plasmodial, and in vivo malaria chemoprotective attributes of methanol extract of Z. zanthoxyloides root bark (ME) and its n-hexane (NHF), ethyl acetate (EAF) and n-butanol (NBF) fractions. The in vitro anti-plasmodial activities against drug-resistant strain (K1) of Plasmodium falciparum and malaria chemoprotective properties against chloroquine-sensitive P. berghei in mice by ME and its fractions were evaluated using standard methods. EAF gave the highest inhibitory activities (IC50 = 2.76 mg/ml) against chloroquine-resistant strain (K1) of P. falciparum, followed by ME (IC50 = 5.54 mg/ml), NBF (IC50 =10.96 mg/ml) and NHF (IC50 = 11.47 mg/ml). Compared to malaria-infected-untreated mice, pre-treatment with 400 mg/kg each of EAF and ME suppressed malaria parasite growth by 92% and 81%, respectively relative to 86% by 28 mg/kg chloroquine phosphate. ME and EAF pre-treatment further prevented malaria associated cytopenia unlike infected-untreated mice. These anti-plasmodial and malaria chemoprotective properties could be attributed to phytochemicals in the herbal drugs whose mechanisms of action should be determined in further studies.

Keywords
Anti-plasmodial activity
malaria
malaria chemoprotection
Zanthoxylum zanthoxyloides L.
Poster
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