Antihyperlipidemic and antioxidant effects of phaseolus vulgaris linn in wistar rats | Blazingprojects Postgraduate Thesis
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Antihyperlipidemic and antioxidant effects of phaseolus vulgaris linn in wistar 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 Antihyperlipidemic Effects
  • 2.2Literature Review on Phaseolus Vulgaris Linn
  • 2.3Antioxidant Properties of Phaseolus Vulgaris Linn
  • 2.4Previous Studies on Wistar Rats
  • 2.5Mechanisms of Action in Antihyperlipidemic Effects
  • 2.6Relationship Between Antioxidants and Lipid Levels
  • 2.7Comparison with Other Antihyperlipidemic Agents
  • 2.8Side Effects and Safety Profile
  • 2.9Dosage and Administration
  • 2.10Future Research Directions

Chapter THREE

RESEARCH METHODOLOGY

  • 3.1Research Design and Methodology
  • 3.2Selection of Sample Population
  • 3.3Data Collection Methods
  • 3.4Experimental Setup
  • 3.5Variables and Measurements
  • 3.6Statistical Analysis Techniques
  • 3.7Ethical Considerations
  • 3.8Validity and Reliability

Chapter FOUR

DATA PRESENTATION AND ANALYSIS

  • 4.1Data Analysis and Interpretation
  • 4.2Antihyperlipidemic Effects in Wistar Rats
  • 4.3Antioxidant Effects in Wistar Rats
  • 4.4Comparison with Control Group
  • 4.5Discussion on Findings
  • 4.6Implications of Results
  • 4.7Limitations of the Study
  • 4.8Recommendations for Future Research

Chapter FIVE

SUMMARY, CONCLUSION AND RECOMMENDATIONS

  • 5.1Summary of Findings
  • 5.2Conclusion
  • 5.3Contributions to Knowledge
  • 5.4Practical Implications
  • 5.5Recommendations for Practice

Thesis Abstract

In this study, the antihyperlipidemic and antioxidants activities of the extract and fractions of
Phaseolus vulgaris L. were evaluated. The crude extract (PVE) of dried pulverized plant material
was obtained by maceration in methylene chloride/methanol (11) while the solvent fractions
were obtained by successive solvent-solvent partition in separating funnel between the crude
extract suspended in aqueous medium and solvents of increasing polarity to obtain the n-hexane
fraction (PVHF), ethylacetate fraction (PVEF), and butanol fraction (PVBF) in that
order.Antihyperlipidemic effects of the extracts and fractions were investigated using acute, subacute
and chronic models. In all threemodels, treatment with (PVE) caused significantreduction
(P<0.05) in the lipid profile parameters with the most significance seen in the sub acute study
where total cholesterol was decreased by 38.44%. Triglycerides level was significantly decreased
(P<0.05) by 18.18% in the acute study model.Similarly, very low density lipoprotein (VLDLC)
and low density lipoprotein (LDL-C) wasrespectively decreased by 18.18% and 48.73% in the
acute antihyperlipidemia model. In contrast, high density lipoprotein (HDL-C) level was
significantly (P<0.05) increased in the acute phase by 20.85%.In all study protocols involving
the various fraction there were significant increase(P<0.05) in lipid profile. PVEF (400 mg/kg)
produced- the most significant reduction in total cholesterol level in the acute study with
percentage decrease of 22.10% compared to the control treatment. Triglycerides level was
similarly reduced by 21.59% and 15.91% at PVHF (200 mg/kg) and PVEF (200 mg/kg) with the
acute study.The sub-acute protocol showed significant decrease at PVBF 200 mg/kg percentage
decrease of 17.28%. VLDL-C level for the fraction study showed significant decrease (P<0.05)
at PVHF 200 mg/kg and PVEF 200 mg/kg with percentage decrease of 21.59% and 15.91%
during the acute protocol, the sub-acute protocol showed significant decrease at PVBF 200
mg/kg percentage decrease of 17.28. LDL-C level for fraction extract study showed dose
dependent significance decrease (P<0.05) seen at PVHF 100 mg/kg, PVEF100 mg/kg, and 200
mg/kg with percentage decrease of 47.19%, 41.62% and 53.39% respectively during the acute
protocol, Finally in the chronic protocol a significant decrease was seen with PVHF 200mg/kg,
PVEF 100 mg/kg, and PVBF 200 mg/kg with percentage decrease of 26.03%, 24.82% and
20.05% respectively. HDL-C level for extract study showed dose dependent significant increase
(P<0.05) seen at PVHF 100 mg/kg, PVEF 100 mg/kg and 200 mg/kg with percentage increase
of 30.44%, 28.88% and 30.86%. DPPH reduction and nitric oxide scavenging assays were used
in the investigation of the extract and fractions for the in vitro antioxidant activities study, the
antioxidant activities of the extract and fractions were further determined in vivo in rats.
Antioxidant enzymes and factors such as catalase, glutathione peroxidase, and lipid peroxidation
activities were measured in carbon tetrachloride-treated rats treated with or without the extract
and fractions studies. The highest percentage reduction of DPPH was 80.61% seen with PVEF
and PVBF fraction at 400 mg/kg. The highest percentage reduction of nitric oxide was 75.86%
seen with PVHF at 200 mg/kg. The in vitro study showed significant increased (P<0.05)
scavenging activity with the PVHF and PVEF having scavenging activity comparable with
ascorbic acid. In in-vivo antioxidant assay showed that the Lipid peroxidation levels estimated by
thiobarbituric acid reaction showed no significant (P>0.05) increase or decrease in the serum
MDA of both the treated and untreated group, while in catalase activity estimation showed
significant (P<0.05) increase was seen with PVE 100 mg/kg of 71.05%, Glutathione peroxidise
activity showed the most significant percentage (P<0.05) increase of 76.19% for PVBF 100
mg/kg.The results of the study showed that the extracts and fractions of Phaseolus vulgaris
xiv
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posses anti-hyperlipidemic and antioxidant with the PVEF showing better and more consistent
effects with all protocols used in the investigation.

Thesis Overview

<p> 1.0. INTRODUCTION<br>A large volume of scientific research suggests that in situations of oxidative stress, reactive<br>oxygen species (ROS) are generated and a homeostatic environment between anti-oxidant and<br>oxidation is created. <br></p>

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