Ethanol leaf extract of irvingia gabonensis o’rorke baill mitagates sodium arsenite-induced nephrotoxicity in wistar albino rats

 

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 Literature Review
  • 2.2Historical Perspective
  • 2.3Theoretical Framework
  • 2.4Conceptual Framework
  • 2.5Empirical Studies
  • 2.6Current Trends
  • 2.7Critique of Existing Literature
  • 2.8Research Gaps
  • 2.9Theoretical Contributions
  • 2.10Practical Implications

Chapter THREE

RESEARCH METHODOLOGY

  • 3.1Research Methodology Overview
  • 3.2Research Design
  • 3.3Data Collection Methods
  • 3.4Sampling Techniques
  • 3.5Data Analysis Procedures
  • 3.6Research Ethics
  • 3.7Validity and Reliability
  • 3.8Limitations of Methodology

Chapter FOUR

DATA PRESENTATION AND ANALYSIS

  • 4.1Overview of Findings
  • 4.2Descriptive Statistics
  • 4.3Inferential Statistics
  • 4.4Themes and Patterns
  • 4.5Comparison of Results
  • 4.6Discussion of Key Findings
  • 4.7Implications of Findings
  • 4.8Recommendations for Future Research

Chapter FIVE

SUMMARY, CONCLUSION AND RECOMMENDATIONS

  • 5.1Conclusion and Summary
  • 5.2Summary of Findings
  • 5.3Contributions to Knowledge
  • 5.4Practical Applications
  • 5.5Limitations of the Study
  • 5.6Recommendations for Practice
  • 5.7Recommendations for Further Research
  • 5.8Conclusion and Final Remarks

Project Abstract

<p> </p><div><p>The aim of this study was to investigate the effect of <em>Irvingia gabonensis </em>O’Rorke Baill ethanol leaf extract on kidney function in sodium arsenite-induced toxicity in Wistar albino rats. Forty (40) female Wistar albino rats weighing between 100-161g were grouped into eight (8) groups of five (5) animals each. Group 1 served as the control and was placed on rat feed and water <em>ad libitum</em>.Group 2 was administered 4.1mg/Kg body weight (Kgbw) of sodium arsenite only for 14 days, groups 3, 4 and 5 were administered 4.1mg/Kgbw of sodium arsenite for 14 days and 100mg/Kgbw, 200mg/Kgbw and 400mg/Kgbw of extract, respectively for another 14 days. Groups 6, 7 and 8 were administered 100mg/Kgbw, 200mg/Kgbw and 400mg/Kgbw of extract, respectively for 14 days and treatments lasted for 28 days. Results obtained revealed significant (p&lt;0.05) increases in the serum levels of renal function biomarkers in the groups exposed to sodium arsenite only when compared with control. Treatment with the extract however, at different doses, led to significant (p&lt; 0.05) reductions in serum levels of all assayed renal function biomarkers. Furthermore, treatment with extract only at different doses led to significant (p&lt; 0.05) and non-significant (P˃0.05) reductions in serum levels of assayed renal function biomarkers compared with the control. Ethanol leaf extract <em>Irvingia gabonensis </em>O’Rorke Baill may therefore be of immense therapeutic value in mitigating sodium arsenite-induced kidney dysfunction in Wistar albino rats.</p><p><strong>KEYWORDS</strong>&nbsp;<em>Irvingia gabonensis </em>O’Rorke Baill, Sodium arsenite, Toxicity, Kidney dysfunction, Biomarkers.</p><p></p></div><h3></h3><br> <br><p></p>

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