Brain antioxidant activities of six artemisinin-based combination therapies (acts) in experimental malaria model bi | Blazingprojects Postgraduate Thesis
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Brain antioxidant activities of six artemisinin-based combination therapies (acts) in experimental malaria model bi

 

Table Of Contents


Chapter ONE

INTRODUCTION

  • 1.1Introduction
  • 1.2Background of Study
  • 1.3Problem Statement
  • 1.4Objective of Study
  • 1.5Limitation of Study
  • 1.6Scope of Study
  • 1.7Significance of Study
  • 1.8Structure of the Research
  • 1.9Definition of Terms

Chapter TWO

LITERATURE REVIEW

  • 2.1Overview of Antioxidants
  • 2.2Artemisinin and Antimalarial Therapies
  • 2.3Antioxidant Activities in Malaria
  • 2.4Mechanisms of Action of Artemisinin-based Combination Therapies
  • 2.5Previous Studies on Antioxidant Activities of ACTs
  • 2.6Importance of Antioxidants in Malaria Treatment
  • 2.7Challenges in Assessing Antioxidant Activities of ACTs
  • 2.8Role of Antioxidants in Combating Malaria
  • 2.9Future Directions in Antioxidant Research
  • 2.10Summary of Literature Review

Chapter THREE

RESEARCH METHODOLOGY

  • 3.1Research Design and Methodology
  • 3.2Selection of Study Participants
  • 3.3Data Collection Methods
  • 3.4Measurement of Antioxidant Activities
  • 3.5Experimental Procedures
  • 3.6Data Analysis Techniques
  • 3.7Ethical Considerations
  • 3.8Validity and Reliability of the Study

Chapter FOUR

DATA PRESENTATION AND ANALYSIS

  • 4.1Overview of Research Findings
  • 4.2Antioxidant Activities of ACT A
  • 4.3Antioxidant Activities of ACT B
  • 4.4Antioxidant Activities of ACT C
  • 4.5Antioxidant Activities of ACT D
  • 4.6Antioxidant Activities of ACT E
  • 4.7Antioxidant Activities of ACT F
  • 4.8Comparative Analysis of Antioxidant Activities

Chapter FIVE

SUMMARY, CONCLUSION AND RECOMMENDATIONS

  • 5.1Summary of Research Findings
  • 5.2Discussion of Key Results
  • 5.3Implications of the Findings
  • 5.4Contributions to Existing Knowledge
  • 5.5Recommendations for Future Research
  • 5.6Conclusion and Closing Remarks

Thesis Abstract

Malaria parasite has remained a menace to human immune system as it usually subjects its host to oxidative stress which in turn has an effect on the levels of the antioxidant system due to generation of reactive oxygen species. This study investigated the brain antioxidant activities with six artemisinin-based combination therapies in an experimental malaria model. Forty (40) adult male Swiss albino mice between 20 – 30 g were randomized into 8 groups of 5 animals each. Groups 1 served as the normal control (NC) and were given normal feed and distilled water. Group 2positive control (PC) received 0.2ml of parasitized erythrocyte from a donor mouse. Group 3 was treated with 5.71 mg/kg body weight (ml/kg bw) Artesunate-amodiaquine – AA (CAMOSUNATE®) for 3 days, group 4 received 6.43 mg/kg bw Artesunate-mefloquine – AM (Artequin™) for 3 days, group 5 were given 2.86 mg/kgbw Artesunate-sulfadoxine-pyrimesthamine – ASP (SIMBCURE®) for 3 days, group 6 received 12.5 mg/kg bw Artemisinin-piperaquine – AP(ARTEQUICK®) for 2 days, group 7 received 5.14 mg/kg bw Dihydroartemisinin-piperaquine – DP (P-ALAXIN™) and group 8 received 8 mg/kg bw Artemether-lumefantrine – AL (Coartem®) for 3 days through oral administration after being inoculated with Plasmodium berghei strain intraperitoneally. The mice were then sacrificed by chloroform inhalation after treatment. The mice brain was harvested and the brain homogenates were used for antioxidant assay, also blood sample was obtained through cardiac puncture for parasite estimation. Result for parasitaemia level showed a significant decreased in groups 3, 4, 6, 7 and 8 in order of decreasing efficacy; AM > DP > AP > AA > AL > ASP. Implying the all the ACTs except ASP were efficacious in parasite clearance. AA, AM, AL and ASP groups had significant depleted levels of GSH, SOD, GPx and GST whereas CAT, MDA levels significantly increased with ASP, AP and DP when compared with NC groups. The vitamins showed variant results with the drugs as there were decreased levels of vitamin C in AP and DP groups while all the artesunate combinations elevated the levels of vitamins E and A. In conclusion the ACTs used suppressed the expression of most of the brain antioxidants even after parasite clearance, possibly due early onset of mice recovery from infection.

Keywords; Antioxidants, Artemisinin-based combination therapy, Brain, Malaria.


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