ABSTRACT
Egg consumption is a popular choice for good nutrients, but
by far the egg most often consumed by human is the chicken egg, typically
unfertilized. Quail eggs help treat tuberculosis, asthma, and diabetes and it
can also help prevent kidney, liver, or gallbladder stones. Thus, this study is
aimed at determining quail egg’s dietary effect on the blood sugar and lipid
profile of alloxan induced diabetic rats. The quail egg sample was analyzed for
its various nutritional compositions using the Association of Official Analytic
Chemists (AOAC) methods. Sixty (60) processed quail eggs and shells, using the
cooked-dry method, were administered to thirty six (36) alloxan induced
diabetic rats which were grouped into nine (9) different groups of four (4)
rats each, at varied doses per group for a duration of seven (7), fourteen (14)
and twenty one (21) days. Their lipid profiles were determined using standard
methods while histological analyses were carried out using the standard
paraffin process method (tissue processing method). Results showed that quail
eggs are good sources of protein, lipids and moisture (15.10±0.16%,
31.39±0.26%and 50.18±0.25% respectively). However, the ash and carbohydrate
contents are minimal (1.13±0.09% and 0.65±0.05% respectively). Elemental
analysis indica tes that the shell is a rich source of Calcium, 3000.00mg/100g;
Zinc, 38.15mg/100g; Iron, 175.40mg/100g; Phosphorous, 120.00mg/100g and
Magnesium, 78.00mg/100g. Rats treated with two (2) Raw Quail eggs (2RE) showed
the best performance in terms of lowering the blood glucose level and weight
gain when compared with the insulin treated rats. Statistical analysis of the
blood glucose at intervals (day 7, day 14 and day 21), indicates that for a
mid-term and long-term treatment of diabetes, quail eggs can be of effective
use. Quail egg treatment does not also affect the serum lipid profile of diabetic
rats but can however lower or reduce the level of any risk of diabetic
dyslipidemia. It is concluded that intake of diets rich in magnesium and
leucine, such as a quail egg diet provides, either alone or as part of a
therapeutic regimen, can have beneficial effect in the prevention and
management of type 1 diabetes.
TABLE OF CONTENT
Title Page
Certification
Dedication
Acknowledgement
Table of Contents
List of Tables
List of Figures
Abstract
CHAPTER ONE
1.0 Introduction
1.1 Justification
of Study
1.2 Aims and
Objectives
CHAPTER TWO
2.0 Literature
Review
2.1 Quail
(Coturnix japonica)
2.1.1 The Quail Bird
2.1.2 The Quail Egg
2.2 Chemical
Composition of Quail Egg
2.3 Recommended
Quail Egg Dosage
2.4 Diabetes
Mellitus
2.4.1 Types of
Diabetes Mellitus
2.4.2 Prevention /
Treatment of Diabetes Mellitus
2.5 Serum Lipid
Profile
2.5.1 Purpose for
Lipid Profile Tests
CHAPTER THREE
3.0 Materials and
Methods
3.1 Experimental
Design
3.2 Sample
Collection
3.3 Phase 1
3.3.1 Proximate Analysis
3.3.2 Elemental
Analysis
3.4 Phase 2
3.4.1 Egg Processing
to Powdered Form
3.4.1.1 The Cook-Dry
Method
3.4.2 Egg Shell
Processing to Powdered Form
3.4.3 Dose
Formulation
3.5. Phase 3
3.5.1 Animal
Experiment
3.5.2 Lipid Profile
Test
3.6 Phase 4
3.6.1 Histological
Analysis
3.6.2 Histological
Sample Preparation
CHAPTER FOUR
4.0 Results
4.1 Proximate
Analysis
4.2 Elemental
Analysis
4.3 Animal
Experiment
4.3.1 Effects of
Quail Egg Diet on Blood Glucose Level
4.3.2 Effects of
Quail Egg Diet on Body Weight
4.3.3 Effects of
Quail Egg Diet on Lipid Profile
4.4 Histology
CHAPTER FIVE
5.0 Discussion
5.1 Proximate
Analysis
5.2 Elemental
Analysis
5.3 Blood Glucose
5.4 Weight
Analysis
5.5 Lipid Profile
Analysis
5.6 Histology
5.7 Conclusion
5.8 Recommendations
References
Appendix
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LIST OF TABLES
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Tables
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Pages
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Table 1:
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Recommended Quail egg dosage and
quantity for various ranges of ages
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Table 2:
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Result of
proximate composition of Quail egg, coturnix japonica in
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g/100g (n = 2).
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Table 3:
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Result of analyzed elemental
compositions of Quail egg, coturnix
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japonica (ppm or
mg/l) (n = 2).
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Table 4:
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Result of mean blood glucose in
mg/dl of alloxan induced diabetic rats
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treated with insulin and with
varied doses of processed quail eggs, egg shell
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and raw quail eggs at various
intervals
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Table 5:
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Result of mean body weight in
gramme(g) of alloxan induced diabetic
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rats treated
with insulin and with varied doses of processed quail eggs, egg
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shell and raw quail eggs at
various intervals. -
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Table 6:
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Result of mean lipid profile in
mg/dl of alloxan induced diabetic rats
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treated with insulin and with
varied doses of processed quail eggs, egg shell
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and raw quail eggs after 21 days
of treatment.
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LIST OF FIGURES
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Figures
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Pages
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Fig. 1:
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Bar chart of mean blood glucose
levels of all the groups before
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induction of
diabetes.
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Fig. 2:
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Bar chart of mean blood glucose levels
of all the groups after day 1 of
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Induction of
diabetes. -
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Fig. 3:
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Bar chart of mean blood glucose
levels of all the groups after day 7 of
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Induction of
diabetes. -
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Fig. 4:
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Bar chart of mean blood glucose
levels of all the groups after day 14 of
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Induction of
diabetes. -
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Fig. 5:
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Bar chart of mean blood glucose
levels of all the groups after day 21 of
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Induction of
diabetes. -
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Fig. 6:
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Summary bar chart of the mean
blood glucose levels of all the groups
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at various intervals of treatment
with insulin and with varied doses of
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quail egg diet. -
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Fig. 7:
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Bar chart of mean body weights of
all the groups before induction of
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diabetes.
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Fig. 8:
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Bar chart of mean body weights of
all the groups after day 7of induction
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of diabetes.
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Fig. 9:
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Bar chart of
mean body weights of all the groups after day 14 of induction
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of diabetes.
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Fig. 10:
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Bar chart of
mean body weights of all the groups after day 21 of induction
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of diabetes.
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Fig. 11:
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Summary bar
chart of the mean body weights of all the groups at various
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intervals of
treatment with insulin and with varied doses of quail egg diet.
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Fig. 12:
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Mean Cholesterol levels of all the
groups after 21 days of treatment.
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Fig. 13:
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Mean High Density Lipoprotein
(HDL) levels of all the groups after
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21 days of treatment. -
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Fig. 14:
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Mean
Triglyceride (TG) levels of all the groups after 21 of day treatment.
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Fig. 15:
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Mean Very Low Density Lipoprotein
(VLDL) levels of all the groups
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after 21 days of treatment.
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Fig. 16:
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Mean Low Density Lipoprotein (LDL)
levels of all the groups after 21
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Days of treatment.
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Fig. 17:
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Summary of the mean lipid profile
levels of all the groups after 21 days
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of treatment.
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Fig. 18:
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Liver Section of the Normal/Control
Rats
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Fig. 19:
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Liver Section of the Untreated
Diabetic Rats -
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Fig. 20:
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Liver Section of the Diabetic Rats
Treated with 40 iu/ml of Insulin -
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Fig. 21:
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Liver Section of the Diabetic Rats
Treated with Processed Quail Egg
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And with egg Shell
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Fig. 22:
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Cortical Kidney Section of the
Normal/Control Rats -
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Fig. 23:
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Kidney Section of the Untreated
Diabetic Rats
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Fig. 24:
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Kidney Section of Diabetic Rats
Treated with 40 iu/ml of Insulin
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Fig. 25:
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Kidney Section
of Diabetic Rats Treated with Processed Quail Egg
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And with egg shell
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Fig. 26:
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Line graph of
the mean blood glucose levels of all the groups against the
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Various days interval. -
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Fig. 27:
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Line graph of
the mean body weights of all the groups against the various
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days interval. -
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CHAPTER
ONE
1.0
INTRODUCTION
Good
nutrition affects growth and development of the human body. Nutritional
composition research has shown that eating well-balanced food can improve human
health. Variety of foods, including vegetables, fruits, grain, and protein, are
essential for the full range of nutrients required for good health. The right
balance of calories, protein, fat, carbohydrates, vitamins, and minerals
provides energy and the variety of nutrients for growing children and for
working adults. Foods that are high in fat, sugar, or salt should be limited in
consumption because they do not provide important nutrients. Both the Child and
Adult Care Program (CACFP) meal pattern, and the Pyramid Web site by US
Department of Agriculture, Food and Nutrition Service, encourage eating variety
of foods (US Department of Agriculture, Food and Nutrition Service, 2005).
Egg
consumption is a popular choice for good nutrients, but by a wide margin the
egg most often humanly consumed is the chicken egg, typically unfertilized
(Applegate, 2000). The avian egg is an important source of nutrients,
containing the proteins, lipids, vitamins, minerals, and growth factors
required by the developing embryo, as well as a number of defence factors to
protect against bacterial and viral infection. Moreover, eggs contain
substances with biological functions and activities, i.e. immune proteins,
enzymes, etc. (Hansen et al., 1998; Nowaczewski et al.,
2013), characterized by
anti-adhesive and antioxidant properties, antimicrobial activities,
immunomodulatory, anticancer, and antihypertensive activities, protease
inhibitors, nutrient bioavailability, and functional lipids, highlighting the
importance of egg and egg components in human health and in disease prevention
and treatment (Kovacs-Nolan et al., 2005). Emphasis has been on poultry
birds, whereas nutritive and economic benefits can also be derived from quail
production since the quail bird is fast growing and resistant to more diseases,
especially the Newcastle disease, than the domestic fowl (Oluyemi and Roberts,
2000).
1.1
JUSTIFICATION OF STUDY
With the world facing explosive
increase in diabetes mellitus, there is a serious challenge to primary health
care in developing countries with negative consequences on the economy.
According to the International Diabetes Federation (IDF) 2014 updates, out of
the world seven billion population, 387million people, aged 20–79 y ears
worldwide are diabetic, (IDF, 2014) giving a comparative prevalence of 8.3%,
while 46.3% cases are undiagnosed . In every 7 seconds, a person dies of
diabetes, with 4.9 million deaths in 2014 alone. Seventy seven percent (77%) of
people with diabetes live in low and middle income countries. Africa has a
recorded incidence of 2,150,274 (5.05%) diabetic patients with over 13million
undiagnosed cases. In Nigeria, there are estimated 374,651 diabetic cases, with
over 172,339 undiagnosed cases. These figures account for about 4.64% Nigerian
adults between ages 20-79 living with diabetes. An estimated 105,090 Nigerians
died in 2014 as a result of diabetes. An average diabetic Nigerian spent about
₦43,527.16 (US $178.39) in 2014 due to diabetes treatment (IDF, 2014). With
this alarming prevalence rate, diabetes mellitus poses a major challenge
globally and accounts for a number of disabilities and deaths worldwide.
Currently,
diabetes therapy is based on the use of hypoglycemic drugs (sulfonamides,
biguanides, and insulin), on hygieno-diet measures, exercise, and requires a
lifelong treatment (IDF, 2014). With the level of poverty in developing nations
like Nigeria, the need for a better and cheaper medication cannot be over
emphasized. This informed the need of this study, to use Quail eggs as a cheap
and alternative therapeutic means for the treatment and management of diabetes.
In most recent times (between
2013–2015) in Nigeria , Quail eggs received ample claims and publicity of being
a wonder drug / diet (i.e. being able to treat diabetes and other life
threatening diseases such as anaemia, HIV/AIDS, infertility, high blood
pressure, e.t.c.) (http://quailfarm.co.uk/index.php/quail-and-health). This
study also centred on verifying Quail egg’s acclaimed efficacy in the treatment
and management of diabetes; using alloxan induced diabetic rats as research
models.
Diabetes tends to lower "good" cholesterol levels
and raises triacylglycerol and "bad" cholesterol levels, which
increases the risk of heart disease and stroke. This common condition is called
diabetic dyslipidemia (lipid profile going in the wrong direction).
Dyslipidemia is characterized by elevated low-density lipoprotein–cholesterol
(LDL-C ), triacylglycerol (TG), and total cholesterol (TC) levels, and lowered
high-density lipoprotein–c holesterol (HDL-C) levels (Betteridge, 2000 and
Barrett-Connor et al., 1982). This is a deadly combination that puts
patients at the risk of premature coronary heart disease and atherosclerosis —
a condition where the arteries become clogged with accumulated fat and other
substances. Studies show a link between insulin resistance, which is a
precursor to type 2 diabetes, and diabetic dyslipidemia, atherosclerosis and
blood vessel diseases. These conditions can develop even before diabetes is
diagnosed.
(http://www.heart.org/HEARTORG/Conditions/Diabetes/WhyDiabetesMatters/Cholesterol-
Abnormalities-Diabetes_UCM_313868_Article.jsp#.Vo6zH17a1dg.
accessed 21st Aug., 2015). Insulin
resistance and type 2 diabetes are associated with a clustering of interrelated
plasma lipid and lipoprotein abnormalities, which include reduced HDL
cholesterol, a predominance of small dense LDL particles, and elevated
triacylglycerol levels (American Diabetes Association, 2003). Each of these
dyslipidemic features is associated with an increased risk of cardiovascular
disease. Increased hepatic secretion of large triacylglycerol -rich VLDL and
impaired clearance of VLDL appears to be of central importance in the
patho-physiology of dyslipidemia. Small dense LDL particles arise from the
intravascular processing of specific larger VLDL precursors. Although
behavioural interventions such as diet and exercise can improve diabetic
dyslipidemia, for most patients, pharmacological therapy is needed to reach
treatment goals. There are several classes of medications that can be used to
treat lipid and lipoprotein abnormalities associated with insulin resistance
and type 2 diabetes, including statins, fibrates, niacin, and
thiazolidinediones (American Diabetes Association, 2003). Clinical trials have
shown significant improvement in coronary artery disease after diabetic
dyslipidemia treatment (Betteridge, 2000 and Barrett-Connor et al.,1982).
Insulin
resistance may play a pivotal role in the development of diabetic dyslipidemia
by influencing several factors. In insulin resistance and type 2 diabetes,
increased efflux of free fatty acids from adipose tissue and impaired
insulin-mediated skeletal muscle uptake of free fatty acids increase fatty acid
flux to the liver (Boden, 1997; Kelley and Simoneau, 1994). The fact that free
fatty acid levels are elevated in individuals with impaired glucose tolerance
suggests that insulin resistance associated with elevated free fatty acid
levels occurs before the onset of hyperglycemia (Bluher et al., 2001).
One study conducted in patients without diabetes showed that decreased glucose
utilization in muscle was associated with acute elevation of free fatty acids
(Dresner et al.,
1999). Epidemiologic studies
have also demonstrated a relationship between plasma free fatty acid levels and
insulin resistance (Reaven and Chen, 1988). In the presence of insulin
resistance, free fatty acids from triacylglycerol lipolysis are deposited in
muscle, liver, heart, and pancreas. Notably, agents that lower elevated free
fatty acids, such as the thiazolidinediones (TZDs), have been shown to improve
insulin sensitivity in muscle, liver, and adipose tissues (Mayerson et al.,
2002
and Miyazaki et al., 2002).
Insulin
resistance also increases hepatic lipase activity which is responsible for
hydrolysis of phospholipids in LDL and HDL particles, resulting in the
formation of smaller and denser LDL particles and a decrease in HDL2 (Tan et al., 1995;
Watson et al., 1994 and Zambon et al., 1993).
This study is an attempt to
justify the use of Quail egg diet, a form of behavioural intervention, as an
effective alternative in the treatment and management of diabetic dyslipidemia
in a situation where the alloxan induced diabetic rats become dyslipidemic.
1.2
AIMS AND OBJECTIVES OF THE STUDY
This
study was designed with the following aims and objectives:
1.
To
determine the nutritional and elemental composition of the quail (Coturnix
japonica) egg
– that is, the composition
of both the whole quail egg and its
shell.
2.
To determine the effects of quail (Coturnix
japonica) egg diet on both the blood glucose level and the lipid profile
levels of alloxan induced diabetic albino rats.
3.
To ascertain the histological effect
of a synergetic mixture of processed quail egg and its shell on the liver and
kidney cells of experimental rats.
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