Hypolipidemic Activity of Cyperous
rotundus on CCl4 Induced Dyslipidemia in Rats
Dominic Amalraj A., Parkavi C., Murugaiah K., Dhanaraj
T.S.*
PG Research Dept. of Biochemistry, Enathi Rajappa College, Pattukkottai, Thanjavur Dt. Tamil Nadu, India. Pin: 614 615.
*Corresponding
Author E-mail: ramanisethu@yahoo.com
ABSTRACT:
The objective of the present
study is to evaluate the hypolipidemic activity of Cyperous rotundus on CCl4 induced Dyslipemia
in rat. The aqueous extract of Cyperous rotundus significantly
show the hypolipidimic activation through lipid
profile liver marker enzyme.
KEYWORDS: Hypolipidemic Activity, Cyperous
rotundus, CC14
induced
INTRODUCTION:
Hyperlipidemia is one of the crucial risk factors for the development
of atherosclerosis
subsequent cardiovascular disease. Atherosclerosis or (atheroma) is an accumulation of lipids (mostly
cholesterol), blood components, calcium
deposits in the arteries with passage of time these deposits can get
larger harder forming athermanous
plaques atherosclerosis can provoke angina pectoris myocardial infraction
(disease of the heart), arthritis of the lower limbs (or) cerebral vascular
attack (affecting the arteries of the brain). Atherosclerosis is a major health
problem of middle late adulthood various risk factors have been sited for its for its occurrence e.g
sex, family history, hypertension, smoking, dyslipidemia,
diabetes mellitus etc. Atherosclerotic plaque involves a number of interrelated
events, including modulation of the normal functioning of the vessel wall
endothelium, an alteration in its permeability
entrapment of low-density lipoprotein (LDL) within the vessel wall its oxidative modification (Ross, 1993).
Among various chemical agent, carbon tetrachloricle
(CCl4) has been thoroughly studied for its hepatotoxic
properties. Which in turn increase the accumulation fat in the liver leads to hyperlinidemia C. rotundus
is a trational medicinal Japanease
natural drugs home
remedy for indigestion disorder of stomach
irritation of bowel. (Dassanayake fosberg,
1985; Jase Lapenta, 2000).
Oral
administration of powder of Cyperou rotundus rhizome, 1gm. Twile
daily in 64 patients of obesity produced significant reduction in their body
weight, blood pressure of hypertensive obese patients (Bambhole
VD & Jiddewar 1984).
The
present work was undertaken to evaluate the hypolipidemic
activity of Cyperous rotundus , the following
biochemical parameters were used to access the hypolipidemic
activity of Cyperous rotundus
.
Determine the lipid profile
Analyse liver marker enzyme.
MATERIALS AND METHODS:
Experimental
Designs: Male albino rats of Wistar strain approximately weighing 150-125g were used in
this study. Body weights of the animals were recorded they were divided into 3 groups of 6 animals
each as follows The Experimental protocol was subjected to the scrutiny of
Institutional Animal Ethics Committee
was cleared by the same before starting.
Group
1: Normal control rats were fed with stard diet served as a vehicle control, which
received liquid paraffin at the dose of 3.0 ml/kg intraperitonially.
Group
2: Rats were induced with hepatocellular damage by receiving suspension of Carbon
tetrachloride (CCl4) in liquid paraffin (1:2, v/v, 1ml of CCl4
i.p./kg body weight) once in
alternate days for15 consecutive days.
Group
3: Rats were treated with Cyperous rotundus
orally
(through intragastric
tube) at the dose of 500 mg/kg body weight for every day in addition to CCl4
suspension for alternate days for 15consecutive days.
Collection
of samples:
On
completion of the experimental period, animals were anaesthetized with thiopentone sodium (50mg/kg). The blood was collected
without EDTA as anticoagulant; Serum was separated by centrifugation used for various biochemical analysis.
Biochemical
Parameter:
On
completion of the experimental period, animals were anaesthetized with thiopentone sodium (50mg/kg). The blood was collected
without EDTA as anticoaguiant: serum was separated by
centrifugation used
for various biochemical analyses such as lipid profile (Werner 1981; Allain, 1974; Friedewad’s
1972) liver enzyme (Reitman Frankel 1957).
Statistical
Analysis
The
results were presented as mean SD. Data was statistically analyzed
using student “t” test. P. values set as lower than 0.001, 01, 0.5 were
considered as statistically significant.
RESULTS AND DISCUSSION:
Cyperous rotundus significantly decreased in the activity of SGOT SGPT when
compared to untreated animals.
TABLE
– I Effect of Cyperous rotundus on
SGOT SGPT
|
Group I |
Group II |
Group III |
SGOT (IU/dl) |
28.72±3.01 |
58.66±6.32 |
30.20±4.01 |
SGPT (IU/dl) |
26.1±2.10 |
65.32±3.61 |
25.29±2.10 |
Values
were expressed as mean ± SD for six rats in each group Significantly
different from Group II.
TABLE – II Biochemical parameters of Cyperous rotundus against ccl4 induced Dyslipidemia
Parameters |
Group I |
Group II |
Group III |
Cholesterol (mg/dl) |
133.58±10.21 |
218.6±15.68 |
144±5.30 |
Triglyceride (mg/dl) |
91.05±7.16 |
233.33±9.73 |
81.01±6.09 |
LDL Cholestero (mg/dl) |
81.01±8.76 |
108.13±10.94 |
87.76±9.84 |
VLDL Choleste (mg/dL) |
27.74±2.75 |
126.6±12.16 |
30.15±3.01 |
HDL cholesterol (mg/dl) |
24.78±2.12 |
16.66±1.09 |
25.33±1.50 |
Values were expressed as mean ± SD for six rats in each group.
Significantly different from
group II.
The
concentration of the enzymes released reflects the severity of the damage. SGOT,
SGPT are enzymes normally present in the liver, heart, muscles blood cells. They are basically
located within hepatocytes. So when liver cells are
damaged or die transaminases are released into blood
stream, where they can be measured they are therefore of index of liver injury
(Reitman Frankel, 1957). In the present study,
the increased activity of SGOT SGPT in CCl4 intoxicated
rats as compared with control rats. This elevated activity of these enzymes in
CCl4 induced rats due to mild inflammation in the liver.
Administration of Cyperous rotundus significantly decreased the activity of SGOT, SGPT in CCl4
induced rats.
Cyperous rotundus significantly
decreased in the level of LDL, increase
the level of HDL when compared to untreated. The increased serum cholesterol
levels in CCl4 induced rats were attributable mainly to an increase
in cholesterol in the LDL fraction. This observation is consistent with the
finding that hypercholesterolemia was caused by LDL HDL. Serum LDL cholesterol levels are
known to be regulated by receptor mediated clearance of the lipoprotein
(Ginsberg, 1998), so the increase of serum LDL-C in CCl4 induced rats
is thought to be caused by the reduction of catabolic pathways. High levels of
LDL cholesterol show a positive correlation with atherosclerosis, whereas high
levels of HDL cholesterol have a negative correlation. HDL inhibits the uptake
of LDL by the arterial wall
facilitates the transport of cholesterol from peripheral tissue
to the liver, where its catabolised excreted from the body (Buring
et al., 1992). Administration of Cyperous
rotundus significantly
restored in the level of lipid profile in CCl4 induced rats rats.
CONCLUSION:
Liver
regulates various important metabolic functions. Hapatic damages are associated
with destortion of these metabolic functions. Liver
disease is still a worldwide health problem. Unfortunately, or synthetic drugs
used in the treatment of liver disease are inadequate sometime can have serious
side effects.
Several
plants products are known to exhibits creditable medicinal properties for the
treatment of heart ailment need to be explored to identify their potential
application in prevention therapy of human aliments. The present study
evaluated the hypolipidemic activity of Cyusperous rotundus.
Supplementation with Cyuspeous rotundus on
ccl4 intoxicated rats exerts the following result.
Restored the lipid profile such as
cholesterol, triglyceride, HDL, VLDL LDL cholesterol.
Maintained the liver functions through the maintenance of liver
markers SGOT SGPT.
Thus
Cyperous rotundus treatment
proved to be effective in reducing the extent of lipid peroxidation
improves the lipid profile. The potential hypolipidmic
activity of Cyperous rotundus may
be due to presence of phenolic groups.
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Received on 19.04.2012 Accepted
on 20.05.2012
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Asian J. Pharm. Tech. 2(2): April-June 2012; Page
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