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Title: Seroep
EFFECT OF CAMEL MILK ON PLASMA LIPIDS PROFILE IN INDUCED-HYPERCHOLESTEROLEMIC
RATS
Author:
Barakat, E. Mohamed and N., Z. Idam
ID: 29638-2011
The Editor must ensure that the OJVR publishes only papers which are
scientifically sound. To achieve this objective, the referees are requested to
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(a)
Writing a report on the reverse side of this form,
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CRITERIA FOR JUDGEMENT (Mark "Yes" or "No").
Is the work scientifically sound? Y
Is the work an original contribution? YAre the conclusions justified on the evidence presented? N see below
Is the work free of major errors in fact, logic or technique? no
Is the paper clearly and concisely written?No
Do you consider that the data provided on the care and use of animals (See Instructions to Contributors) is sufficient to establish that the animals used in the experiments were well looked after, that care was taken to avoid distress, and that there was no unethical use of animals? Animal ethics statement required for further consideration
2 PRESENTATION (Mark "Yes" or
"No").
Does the title clearly indicate the content of the paper? NO (see suggestions)
Does the abstract convey the essence of the article? NO (see changes)
Are all the tables essential? Y
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Reassess after major changes
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4.REPORT: This is a report of lipid serum data derived
from feeding rats camels milk. There are no conclusions and the same results
are presented 3 times! The report description of methods and results are hard
to follow and confusing. Table 1 suffices for results which should be
discussed. Figure 1 simply repeats table data and the text does so again. Abstract
says 21 rats but how many per group needs to be stated otherwise the statistics
are useless. The work needs to be redefined what are the conclusions? Does
camel milk have any effect of plasma lipids or not and if so, which one? It
would appear that the only effect was that both cholesterol and/or camel milk
may have reduced HDL-c. This is a barely pass work and authors will have to
re-submit.
TITLE change see suggestions
Completely
re-write see suggested below:
ABSTRACT: The aim of this study was to investigate the effect of raw camel milk
on plasma lipids profile in rats fed on cholesterol enriched diet. Twenty one Wistar albino rats were divided into three groups A, B and
C, Group A was used as a control group and was given only standard rats diet,
group B received a diet containing 1% cholesterol and group C received a diet
containing 1% cholesterol in addition to 16 ml/kg Bwt
raw camel milk twice daily for 4 weeks. The results showed that there was a
significant (P<0.05) increase in the level of plasma total cholesterol (TC),
low density lipoprotein-cholesterol (LDL-c) and triglycerides (TG) in group B (CHOLESTEROL
ONLY GROUP) compared to the control group. The plasma levels of TC, LDL-c and
TG in group C were insignificantly deceased compared to the control group.
However, there was no significant difference between groups B and C despite the
decease in group C. The level of plasma HDL-c was
significantly (P<0.05) lower in group B and group C compared to the control
group (group A). There was no significant difference between group B and C with
respect to HDl-c level.
Key
words: camel milk, cholesterol ,Coronary heart disease
IThe effect of
raw camel milk on plasma lipids in rats fed a cholesterol enriched diet was
investigated. Wistar albino rats were fed a standard
diet (controls), 1% cholesterol or 1% cholesterol with 16 ml/kg raw camel milk
twice daily for 4 weeks. Results showed a significant (P<0.05) increase in
plasma total cholesterol (TC), low density lipoprotein-cholesterol (LDL-c) and
triglycerides (TG) in rats fed 1% cholesterol compared to the control group.
Plasma TC, LDL-c and TG in rats fed camel milk did not decrease compared with
controls. There was no significant difference between rats fed 1% cholesterol
and those given camel milk. Plasma HDL-c was significantly (P<0.05) lower in
rats given 1% cholesterol compared with controls but no difference with those
fed camel milk
INTRODUCTION
Delete not required old story:
Hypercholesterolemia is a major risk factor associated with heart disease.
Coronary heart disease (CHD) is the most common form of heart disease rises
with high plasma LDL-c concentration which carries most of the circulating
plasma cholesterol(2). Epidemiological studies demonstrated that there is a
continuous increase in the risk of death from CHD with increasing serum cholesterol(7). Keeping blood cholesterol at desirable level
is the fundamental choice for controlling this disease. Changes in the diet
plays an important role in reducing plasma cholesterol(2).
Relevant
use this:see suggestedCamel milk? is an important nutrient
source for human which represent the only source of protein in tropical and
sub-tropical regions(5). It differs from other ruminants milk having low sugar,
low cholesterol, high minerals(9) and high amount of vitamin C which is three
times higher than that of bovine milk(6). Camel milk contains high amount of
poly-unsaturated fatty acids which are essential for human nutrition and may
lower human serum lipids, hence it lead to a decrease incidence of lipids
related cardiovascular disease(8). It was reported
that vitamin C is necessary for cholesterol transformation to the bile acids at
the rate limiting step of bile acids biosynthesis(13).
The hypocholesterolemic activity of vitamin C is due
to the enhancement of cholesterol 7-α hydroxylase
enzyme which is involved in the catabolism of cholesterol. Because of the high
amount of vitamin C in camel milk and its role as an antioxidant therefore, the
study aim to investigate the effect of raw camel milk on plasma total
cholesterol, LDL-c, HDL-c and triglycerides in induced hypercholesterolemic
rats.
MATERIAL
AND METHODS
Experimental
animals:
Twenty one adult male Wistar albino rats weighing 85-120 g were used in this
study. They were housed in premises of the Medicinal and Aromatic Plant
Research Institute, Sudan. All rats were fed with standard diet and
acclimatized in standardized condition for 7 weeks before starting the
experiment.
Experimental
procedure:
The rats were divided into three groups
named A, B and C of seven rats each. Group A was fed with standard diet and
used as untreated control, group B received a diet containing 1% cholesterol
(for induction of hypercholesterolemia) while group C received a diet
containing 1% cholesterol in addition to 16 ml/kg body weight (Bwt) of raw camel milk twice daily, which was given orally
via a gastric tube. The experimental period was 4 weeks.
Blood
samples condition:
Blood samples were collected every two
weeks interval during the experimental period, after an over-night fast. Blood
was drawn from the orbital plexus by capillary glass tubes(11)
and collected in lithium leparin containers. The
tubes were centrifuged at 5000 rpm for 10 min. for the separation of plasma.
Biochemical
analysis:
Plasma total cholesterol, LDL-c, HDL-c
and triglycerides were estimated by using fully automated and computerized
Roche Diagnostic Hitachi 902 Analyzer, employing enzymatic photometric assay.
Statistical
analysis:
Data was analyzed using complete
randomized design to separate the means and standard error with the aid of a
computer package program (SPSS). The significant differences between groups
were evaluated using general linear model of statistical analysis system (12).
RESULTS
AND DISCUSSION
See suggested
below: Results: The results of plasma total cholesterol, HDL-c, LDL-c and
triglycerides of groups A, B and C were presented in
Results
1 Table (1) and
Same
results again
Fig. (1).
Same
results in text again! There was a significant (P<0.05) increase in
the level of plasma total cholesterol in group B (cholesterol untreated group)
and C (cholesterol fed treated group) compared to the control group. However
the increase is more in group B compared to group C with no significant
difference.
The level of plasma HDL-c was
significantly (<0.05) lower in group B and C compared to the control group.
The plasma levels of LDL-c of groups B
and C was significantly (P<0.05) higher compared to the control group. In
group C the level of plasma LDL-c was non-significantly lower compared to group
B.
The plasma level of triglycerides was
significantly (P<0.05) higher in group B and C compared to the control
group. While there was no significant difference between group C and group B
despite the lower level of triglycerides in group C.
Discussion:
There is an increasing global concern about the role of the food in health and
disease. The concept is consistent with historic belief that natural substances
play an important role in prevention and treatment. Camel milk is of putative hypocholesterolemic effect in Sudanese traditional medicine
(personal communication, 2007). Therefore, the aim of the present study was to
evaluate the effect of raw camel milk nutrients on the levels of plasma lipids
profile in induced hypercholesterolemic rats.
The study showed that administration of
16 ml/kg Bwt of raw camel milk twice daily caused
insignificant decrease in the levels of plasma total cholesterol, LDL-c, and
triglycerides compared to the control group. This decrease corresponds to
(10.32%), (23.06%) and (3.69%) for total cholesterol, LDL-c and triglycerides
respectively in comparison with cholesterol fed untreated group (group B). The
results revealed that there was a significant (P<0.05) decrease in the
levels of plasma HDL-c in camel milk treated group compared to the control
group. These findings are in line with Agrawal et al.(1) who reported that the oral administration of 500 ml of
raw camel milk for three months did not significantly affect the levels of
plasma lipid profiles of type one diabetic patients. Similar result was found
by Mahamad et al.(10) who reported that camel milk
have no significant effect on the serum lipids profile at 500 ml/kg Bwt when it was given to type 1 diabetic patients for 4
weeks. The effect of camel milk on cholesterol is attributed to vitamin C
content which acts as antioxidant. The insignificant effect reported in this
study may be due to the fact that vitamin C which is found in camel milk is not
quite enough to decrease the plasma cholesterol level. Also the gazing area
affects milk composition.
In contrat Elayan et al. (4) found hypocholesterolemic
effect of fermented camel milk (gariss) in
diet-induced hypercholesterolemic rats. They reported
that supplementation of 0.5 g gariss for 6 weeks
reduced the level of plasma total cholesterol, LDL-c and triglyceride with no
significant effect on HDL-c. Suzuki et al.(14)
reported that fermented dairy product have been recommended as dietary
supplement because of their hypocholesterolemic
effect. The source of variation may be due to the fact that fermented milk
contains more hypocholesterolemic factors greater
than milk(3).
This
is enough!
Table (1): Values of plasma lipids profile of
induced hypercholesterolemic
Wistar albino rats.
|
Group Parameters |
A |
B |
C |
|
Total
cholesterol (mg/dl) |
81.76 ± 1.98b |
150.00 ± 15.49b |
134.52 ± 14.84a |
|
HDL-c
(mg/dl) |
47.77 ± 1.83a |
33.30 ± 1.44b |
34.79 ± 1.87b |
|
LDL-c (mg/dl) |
27.65 ± 1.80b |
107.40 ± 14.78a |
82.63 ± 13.12a |
|
Triglycerides
(mg/dl) |
73.29 ± 5.47b |
93.95 ± 6.6a |
90.48 ± 4.87a |
Means (±SE)
with the same row having different superscript small letters are significantly different
at (P<0.05).
Group A: Fed standard diet, Group B:Fed standard diet with 1% cholesterol, Group C: Fed standard diet with1%
cholesterol and 16 ml/kg Bwt camel milk
Table
(1): Values of plasma lipids profile of induced hypercholesterolemic
Wistar albino rats.
Group
Parameters A B C
Total
cholesterol (mg/dl) 81.76 ± 1.98b 150.00 ± 15.49b 134.52 ± 14.84a
HDL-c
(mg/dl) 47.77 ± 1.83a
33.30 ± 1.44b
34.79 ± 1.87b
LDL-c
(mg/dl) 27.65 ± 1.80b 107.40 ± 14.78a 82.63 ± 13.12a
Triglycerides
(mg/dl) 73.29 ± 5.47b
93.95 ± 6.6a 90.48 ± 4.87a
Means
(±SE) with the same row having different superscript small letters are
significantly different at (P<0.05).
Group A: Fed standard diet
Group B: Fed standard diet with 1% cholesterol
Group C: Fed standard diet with1% cholesterol and
16 ml/kg Bwt camel milk
Panel (A) Panel (B)
Panel (C) Panel (D)
Fig.(1): The effect of camel milk on plasma total cholesterol,
LDL-c, HDL-c and triglycerides in
induced hypercholesterolemic Wistar
albino rats.
Bars
having different superscript small letters are significantly different at
(P<0.05).
Group A:
Fed standard diet.
Group B:
Fed standard diet with 1% cholesterol.
Group C: Fed
standard diet with 1% cholesterol and given orally 16 ml/kg Bwt
raw camel milk.
References
1. Agrawal. R. P., swami, S.C., Beniwal,
R., Kochar, D. K., Sahani,
N. S., Tuteja, F. C. and Ghouri,
S. K. (2003). Effect of the camel milk on glycemic
control, risk factors and diabetes quality of life in type-1 diabetes. A randomized prospective controlled study. J. Camel Pract. Res. 10 (1): 45-50.
2.
Davidson, S. (2002). Principles and Practice of Medicine.19th
edition, U.S.A. pp. 357-478.
3. Eichholzer, M. And stahelin,
H. (1993). Is there a hypocholesterolemic
factors in milk and milk products. Int. J. Vitam. Nutr.
Res. 63: 159-67.
4. Elayan, A. A., Sulieman, A. M.,
and Saleh, F.A. (2008). The hypocholesterolemic
effect of gariss and gariss
containing Bifidobacteria in rats fed on a
cholesterol-enriched diet. Asian J. Bioch.
3 (1): 43-47.
5. Farah,
Z. (1996). Camel milk: properties and products. SKAT, Swiss center for
development cooperation in technology and management. St. Gallen,
Switzerland.
6. Farah,
Z., Rettenmaier, R. and Atkins, D. (1992). Vitamin content of camel milk. Int. J. Vit.
Nutr.
62: 30-33.
7. Gorban, A. M. and Izzeldin, O. M.
(2001). Fatty acids and lipids of camel milk and colostrums.
Int. J. Food Sci. Nutr. 52:
283-287.
8.
Griffin, M., Frazer, A., Collins, P., Owens, D. and Tomkin,
G. (1998). Cellular cholesterol synthesis and
atherosclerosis. Atherosclerosis. 138(2):
313-318.
9. Knoess, R. H. (1979). Milk production of
dromedary. In: camels. IFS. Symposium, Sudan,
10-201.
10. Mahamad, R. H., Salama, O., Hegazi, A. G., El-shaieb, S. and
Al-mehdar, H. (2006). Camel milk as
an alternative therapy for treatment of type 1 diabetes. proceeding of eighth world
conference of scientific miracles, Kuwait.
11. Nagappa, A. N., Thakurdesai, P.
A., Venkat, N. and Singh, J. (2003). Anti-diabetic activity of Terminalia actappa linn fruits. J. Ethnopharmacol. 88: 45-50.
12. SAS
(1998). SAS institute, NC, U. S. A.
Simon,
J. A. and Hudes, E. S. (2000). Serum ascorbic
acid and gall bladder disease. Arch. Int. Med. 160 (7): 931-936.
Suzuki,
Y. H., Kaizu, H. and Yamauchi, Y. (1991). Effect of
cultured milk on serum cholesterol cocenterations in
rats fed high- cholesterol diets. Anim. Sci. Technol. 62: 565-571.