Effects of ethanol extracts of euphorbia hirta herb on some oxidative and biochemical parameters in alloxan-induced diabetic rats
Table Of Contents
Chapter ONE
INTRODUCTION
- 1.1Introduction
- 1.2Background of Study
- 1.3Problem Statement
- 1.4Objectives 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 Diabetes
- 2.2Alloxan-Induced Diabetes in Animals
- 2.3Oxidative Parameters in Diabetes
- 2.4Biochemical Parameters in Diabetes
- 2.5Euphorbia Hirta Herb
- 2.6Ethanol Extraction Process
- 2.7Previous Studies on Euphorbia Hirta
- 2.8Effects of Euphorbia Hirta on Oxidative Parameters
- 2.9Effects of Euphorbia Hirta on Biochemical Parameters
- 2.10Summary of Literature Review
Chapter THREE
RESEARCH METHODOLOGY
- 3.1Research Design
- 3.2Sampling Method
- 3.3Experimental Animals
- 3.4Induction of Diabetes
- 3.5Administration of Euphorbia Hirta Extracts
- 3.6Measurement of Oxidative Parameters
- 3.7Measurement of Biochemical Parameters
- 3.8Data Analysis Techniques
Chapter FOUR
DATA PRESENTATION AND ANALYSIS
- 4.1Characteristics of Experimental Animals
- 4.2Effects of Euphorbia Hirta Extracts on Oxidative Parameters
- 4.3Effects of Euphorbia Hirta Extracts on Biochemical Parameters
- 4.4Comparison with Previous Studies
- 4.5Discussion on the Findings
- 4.6Implications of the Results
- 4.7Limitations of the Study
- 4.8Recommendations for Future Research
Chapter FIVE
SUMMARY, CONCLUSION AND RECOMMENDATIONS
- 5.1Summary of Findings
- 5.2Conclusion
- 5.3Contribution to Knowledge
- 5.4Practical Implications
- 5.5Areas for Further Research
Project Abstract
<p> Diabetes mellitus produces a lot of highly reactive oxygen species which have been attributed to the aetiology and pathophysiology of the disease. In view of the adverse effects associated with synthetic drugs and natural medicine being considered to be safer, cheaper and more effective, traditional antidiabetic plants can be explored. The results of the experiment showed that there were significant increases (P<0.05) in the concentrations of total cholesterol, low density lipoprotein (LDL) and triacylglycerol (TAG) in group 2 rats (diabetic untreated) compared with normal control rats (group 1). Administration of 300 mg/kg b.w. of ethanol extracts of Euphorbia hirta to rats in group 3 to 6 and 0.01mg/kg b.w of voglibose to rats in group 7 showed significant reduction (p<0.05) in total cholesterol, LDL and TAG concentrations. On the other hand, there was significant decrease (p<0.05) in high density density (HDL) concentrations in the group 2 (diabetic untreated) compared with group 1 (normal rats). However, administration of 300 mg/kg b.w of ethanol extracts of E. hirta to rats in group 3 to 6 and 0.01 mg/kg b.w to rats in group 7 showed significant increase (p<0.05) in HDL concentration. There was no significant increase (p>0.05) in sodium and bicarbonate ion concentrations but significant increase (p<0.05) in potassium and chloride ion concentrations in diabetic untreated rats (group 2) compared with rats in normal control group. There was significant increase (p<0.05) in serum urea and creatinine concentrations in diabetics untreated rats (group 2) compared with normal rats (group 1). Administration of 300 mg/kg b.w. of ethanol extract of E. hirta to groups 3 to 6 and 0.01 mg/kg b.w. of voglibose to group 7 resulted in significant decrease (p<0.05) in serum urea and creatinine concentrations. There was significant decrease (p<0.05) in serum catalarse and superoxide dismutase activities and vitamin C concentration with significant increase (p<0.05) in serum malondialdehyde concentration in group 2 (diabetics untreated rats) compared with normal rats (group 1). However, addition of 300 mg/kg b.w. of ethanol extract of E. hirta to Groups 3 to 6 and 0.01 mg/kg b.w. of voglibose to group 7 resulted in significant increase (p<0.05) in serum catalase and superoxide dismutase activities and vitamin C concentration, with significant decrease (p<0.05) in MDA concentration compared with the diabetic untreated rats (group 2). There was significant increase (p<0.05) in blood glucose concentration in rats of group 2 to 7 before administration of ethanol extracts of E. hirta and voglibose compared with normal rats (group 1). When 300 mg/kg b.w. of ethanol extract of E. hirta was administered to groups 3 to 6 and 0.01 mg/kg b.w. of voglibose to group 7, there was significant decrease (p<0.05) in blood glucose concentration compared with diabetic untreated (group 2). The administration of 300 mg/kg b.w. of ethanol extract of E. hirta and 0.01 mg/kg b.w. of voglibose showed significant increase (p<0.05) in the body weights of the rats in groups 4 to 7 compared with that of normal control. No significant increase (p>0.05) in the body weights of rats in group 2 and 3 compared with normal rats (group 1). When 300 mg/kg b.w. of ethanol extract of E. hirta and 0.01 mg/kg b.w. of voglibose were administered to rats in groups 3 to 7, there was significant increase (p<0.05) in the body weights of the rats compared with diabetic untreated rats (group 2). <br></p>
Project Overview