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Article ; Online: Antimalarial Activities of a Therapeutic Combination of Azadirachta indica, Mangifera indica and Morinda lucida Leaves: A Molecular View of its Activity on Plasmodium falciparum Proteins.

Abdulai, Suliat Iyabode / Ishola, Ahmed Adebayo / Bewaji, Clement Olatunbosun

Acta parasitologica

2023  Volume 68, Issue 3, Page(s) 659–675

Abstract: Background: The search for new antimalarial drugs remains elusive prompting research into antimalarial combinations from medicinal plants due to their cheapness, efficacy and availability. Azadirachta indica (AI), Morinda lucida (ML) and Mangifera ... ...

Abstract Background: The search for new antimalarial drugs remains elusive prompting research into antimalarial combinations from medicinal plants due to their cheapness, efficacy and availability. Azadirachta indica (AI), Morinda lucida (ML) and Mangifera indica (MI) have all been reported as potent antimalarial plants.
Purpose: This study evaluated the efficacy of an antimalarial combination therapeutics prepared from leaves of AI, ML and MI using in vitro, in vivo and molecular methods.
Methods: Refined extracts of the plants combination was made by partitioning the aqueous extract of plants combinations (AI + MI, AI + ML, MI + ML, AI + MI + ML) using methanol and ethyl acetate consecutively. The resulting ethyl acetate partitioned fraction was evaluated for its antimalarial activity. Molecular docking and molecular dynamics simulation were employed to determine the possible mechanism of action of the constituent of the most active combination against four important P. falciparum proteins.
Results: The result revealed that the refined extract from combinations AI + ML and MI + ML at 16 mg/kg bodyweight have the highest chemo-suppressive effect of 90.7% and 91.0% respectively compared to chloroquine's 100% at 10 mg/kg. Also, refined extract from MI + ML combination improved PCV levels significantly (p < 0.05) compared to controls. Molecular docking revealed oleanolic acid and ursolic acid as multiple inhibitors of plasmepsin II, hiso-aspartic protease, falcipain-2 and P. falciparum Eonyl acyl-carrier protein reductase with relative stability during 100 ns of simulation.
Conclusion: The study unveiled the potentials of ML and MI as good candidates for antimalarial combination therapy and further established their use together as revealed in folklore medicine.
MeSH term(s) Antimalarials/pharmacology ; Antimalarials/therapeutic use ; Azadirachta ; Plasmodium falciparum ; Morinda ; Mangifera ; Malaria ; Plant Extracts/pharmacology ; Molecular Docking Simulation ; Plant Leaves
Chemical Substances Antimalarials ; ethyl acetate (76845O8NMZ) ; Plant Extracts
Language English
Publishing date 2023-07-21
Publishing country Switzerland
Document type Journal Article
ZDB-ID 1132735-2
ISSN 1896-1851 ; 0065-1478 ; 1230-2821
ISSN (online) 1896-1851
ISSN 0065-1478 ; 1230-2821
DOI 10.1007/s11686-023-00698-7
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