Anti-Inflammatory Activity of Butea monosperma Leaves
Swati
Jain, Nilesh Gupta, U.K. Jain*, A.S. Raghuvanshi and Ajay Patel
Bhopal Institute
of Technology and Science-Pharmacy Bhojpur Road, Bangrasia, Bhopal (M.P.),
462045
ABSTRACT:
Methanolic extract of leaf of Butea monosperma
was evaluated for Anti-inflammatory activity on carrageenan induced models, in
albino rats. The activity was found to be dose dependant. Overall results of
this study suggest that the extract possesses significant anti-inflammatory
activity.
KEYWORDS: Butea monosperma, Methanolic extract, Anti-inflammatory activity, Carrageenan.
INTRODUCTION
Inflammation is a local response of living mammalian
tissues to injury. It is a body defense reaction in order to eliminate or limit
the spread of injurious agent. Anti-inflammatory are the drugs or medicines
used to relieve swelling, pain and other symptoms of inflammation. These used
to reduce the inflammatory response to infections agents, Trauma, Surgical
procedures or in musculoskeletal muscle1. Butea monosperma, belonging to family- Papilionaceae, is widely
used medicinal plant in traditional system with a wide range of biological
activities.
It is a tree of moderate size found in India, Burma and
Ceylon. Roots are used in night blindness and elephantiasis. Flowers are used
as diuretic, astringent and in diarrhea. The bark is used as appetizer,
anti-inflammatory, biliousness, as an antidote in treatment of snakebite2.
A review of literature did not reveal any information on the anti-inflammatory
studies. Hence in the present work anti-inflammatory activity of the leaf
extract of Butea monosperma was
studied.
MATERIAL AND METHODS:
Plant material The leaves of Butea
monosperma was collected from Gairatganj District Raisen (MP) in March and
authenticated in Bhopal Institute of Technology and Science-Pharmacy Bhopal. A voucher specimen has been deposited in
our laboratory for further reference.
Preparation of extract Collected leaves were dried in shade and processed to a
coarse powder. This powder was subjected to solvent extraction with methanol in
a soxhlet apparatus. After exhaustive extraction, the methanolic extract was
dried at low temperature under reduced pressure in a rotary evaporator to
obtain greenish-black colored residue used for anti-inflammatory activity
studies.
Anti-inflammatory activity The anti-inflammatory activity was carried
out on Healthy Albino rats as per the animal ethical protocol. Animal study was
performed in division of Pharmacology, Bhopal Institute of Technology and
Science-Pharmacy Bhojpur Road, Bangrasia, Bhopal with due permission from Institutional animal
ethical committee.
Healthy Albino rats of either sex, weighing between
100-120 gm were selected for the studies. Rats were allowed to take standard
lab feed, water and ad libidum in the
animal house and were maintained in clean and hygienic conditions. For
carrageenan induced rats hind paw edema model, rats were divided into 4 groups
containing 6 animals per group.
The control group was given a 1%
sodiumcarboxymethylcellulose solution. Group II of animals received 5 mg/kg of
diclofenac sodium, which was considered as standard. The experimental group III
and IV were treated with 200 and 400 mg/kg of methanolic extract respectively
dissolved in sodiumcarboxymethylcellulose solution. Doses were given orally
with the help of an oral catheter. 0.1 ml of 1% solution of carrageenan was
administered to the rats in to the planter surface of the right hind limb to
induce paw edema. Paw volume was measured plethysmographically after 3 h of
carrageenan injection and paw swelling in groups of treated were compared with
control. Percentage inhibition of edema was calculated by using the following
formula3.
% Inhibition =
Vc-Vt/ Vc * 100
Where, Vt - mean increase in paw volume in rats treated
with test compounds.
Vc - mean increase in paw volume in control group of
rats.
TABLE
1: Anti-inflammatory Activity of Butea monosperma leaf
Extracts Against Carrageenan Induced Paw Edema in Rats
Group |
Dose (mg/kg) |
Mean paw volume + S.D after 3 hrs. |
% Inhibition of edema |
Control |
10 mg/kg |
0.210 + 0.0039 |
_ |
Standard |
5 mg/kg |
0.060 + 0.0012 |
71.4% |
Methanolic Extract |
200mg/kg. |
0.156 + 0.0031* |
25.71% |
Methanolic Extract |
400mg/kg. |
0.104 + 0.0019** |
50.48% |
(Mean ± SEM, n = 6), P value
< 0.05*
Statistical Analysis -Result were analysed by Student's t-test.
The Minimum level of significance was fixed at P<0.05.
RESULT:
Anti-inflammatory activity of Butea monosperma leaf
extracts against carragenan induced
paw edema is shown in Table I. The methanolic extract at the dose level of 400
mg/kg body weight and diclofenac sodium at the dose of 5 mg/kg exhibit
significant (P<0.05) anti-inflammatory activity whereas methanolic extract
(200 mg/kg) did not show such significant activity when compared with
carrageenan control.
DISCUSSION:
Apart from modern medical therapy, the use of herbal
drugs in the treatment of inflammatory diseases is a common practice in many
countries of Asia including India and Bangladesh. A number of medicinal plants
have been reported4-6 to be effective against inflammatory, as they
are used in traditional herbal practice. In Indian system of medicine certain
herbs are claimed to provide relief of pain and inflammation. Carrageenan
induced inflammation is a useful model to detect oral action7 of
anti-inflammatory agents. The development of edema8 in the paw of
the rats after the injection of carrageenan is due to release of histamine,
serotonin and prostaglandin like substance. The significant activity of the
methanolic extract and the standard drug observed in the present study may be
due to the inhibition of mediators of inflammation such as histamine, serotonin
and prostaglandin. The present study was undertaken to find out the scientific
rationale factor responsible for anti-inflammatory activity.
ACKNOWLEDGMENTS:
The authors are thankful to Bhopal Institute of
Technology and Science-Pharmacy Bhojpur Road, Bangrasia, Bhopal for
providing facilities to carry out the research work.
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Received on 24.07.2010
Accepted on 11.08.2010
© A&V Publication all right reserved
Research J. Pharmacology and
Pharmacodynamics. 2(5): Sept.-Oct. 2010, 351-352