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Am. J. Biomed. Sci. 2022,14(3), 136-145; doi:10.5099/aj220300136 |
Amodiaquine-Azithromycin Eradicates Blood and Liver Stages of Plasmodium berghei Infection in Mice |
Elias Adikwu
1, Igono Simeon Ajeka
2, Confidence Ogechi Nworgu
2 |
1 Department of Pharmacology
/Toxicology, Faculty of Pharmacy, Niger Delta University, Bayelsa State,
Nigeria |
2 Department of Biology, Faculty of Natural and Applied
Sciences, Ignatius Ajuru University of Education, Rumuolumeni, Port Harcourt, Rivers State, Nigeria |
*Corresponding
Author |
Elias Adikwu |
Department of Pharmacology
/Toxicology, Faculty of Pharmacy, Niger Delta University |
Bayelsa State |
Nigeria |
Email: adikwuelias@gmail.com |
Tel: +2347068568868 |
Abstract Amodiaquine (AQ) is used as a
partner drug with artemisinins for malaria treatment.
Azithromycin (AZ) is a macrolide antibiotic with potential antiplasmodial
activity. This study assessed
whether AZ can be used as a partner drug with AQ for malaria treatment in Plasmodium
berghei-infected mice. Adult Swiss albino mice
(30-35g) of both sexes were randomly grouped and used. The mice were inoculated
with Plasmodium berghei and orally treated with AQ (10 mg/kg), AZ (10 mg/kg) and AQ-AZ,
respectively. Chloroquine CQ (10mg/kg) was used as the standard. At the
termination of treatment, blood samples were collected and assessed for
percentage parasitamia, inhibition and hematological
markers. Liver samples were examined for histological changes. The mice were
also observed for mean survival time (MST). In the curative, prophylactic and
suppressive tests, AQ-AZ significantly decreased percentage parasitamia
with difference observed at p<0.05 when compared to AQ or AZ. Curatively,
AQ, AZ and AQ-AZ produced 71.41 %, 66. 80% and 92.60% parasitamia
inhibitions, respectively when compared to 88.20% produced by CQ. The curative,
prophylactic and suppressive tests showed significant prolongation of MST by
AQ-AZ with difference observed at p<0.05 when compared to AQ or AZ. AQ-AZ
inhibitions of Plasmodium berghei-induced
alterations in hematological makers were characterized by increased red blood
cells, packed cell volume, hemoglobin and decreased white blood cells with
difference observed at p<0.05 when compared to AQ, or AZ. AQ-AZ eradicates
vascular congestion and inflammatory cells observed in the liver of Plasmodium
berghei-infected mice. AZ can be used as a
partner drug with AQ for the treatment of malaria. |
Keywords: Amodiaquine, Azithromycin, Partner-Drug, Plasmodium, mice |
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