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African Journal of Traditional, Complementary and Alternative Medicines
African Ethnomedicines Network
ISSN: 0189-6016
Vol. 4, Num. 4, 2007, pp. 411 – 416
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African Journal of Traditional, Complimentary and Alternative Medicines,
Vol.4,
No. 4, 2007, pg. 411 – 416
Research Paper
ANTI-INFLAMMATORY AND ANTI-NOCICEPTIVE ACTIVITIES OF METHANOLIC
EXTRACT OF THE LEAVES OF FRAXINUS FLORIBUNDA WALLICH
Sutharson Lingadurai*1, Lila Kanta Nath1, Prasanna Kumar Kar1, Shila E.Besra2,
Rajan
Vedasiromani Joseph2
1Department of Pharmacology, Himalayan Pharmacy Institute, Majhitar, Rangpo, Sikkim-737136, India. 2Drug Development Division, Indian Institute of Chemical Biology, Kolkata700032, India.*E-mail: apjak_son@yahoo.co.in Tel.: +91 9932232464; Fax: +91 3592 246247
Code Number: tc07058
Abstract
Fraxinus floribunda Wallich (Family-Oleaceae) is a wide green tree in
the sub-alpine region of Sikkim, India. The methanolic extract of the leaves
of Fraxinus floribunda (MEFF) at 100, 200 and 400mg/kg/p.o was screened
in rats for anti-inflammatory activity by acute-carrageenan induced paw edema,
sub-acute cotton pellet induced granuloma and chronic Freund's adjuvant
induced arthritis models. In all the three models of antiinflammatory studies
200 and 400mg/kg/p.o doses of the extract showed significant effect (P<0.001).
Antinociceptive evaluation was performed by writhing and tail-immersion tests
in mice. Anti-nociceptive evaluation revealed that MEFF at the dose of 400mg/kg/p.o
had significant activity against the control. The relieving effect was through
the peripheral and central mechanism of action of the extract. This study rationalized
the ethno medicinal use of the plant for relieving pain in inflammatory pathological
conditions like fracture and dislocation.
Key Words: Fraxinus floribunda, Carrageenan, Cotton pellet, Freund's
adjuvant, Writhing test, Tail immersion test.
Introduction
Inflammation is an important causative agent of human morbidity and mortality,
such as Systemic Inflammatory Response Syndrome (SIRS), Multiple Organ Dysfunction
Syndrome (MODS), and Multiple Organ Failure (MOF) (Baeu et al.,1998). Fraxinus
floribunda Wallich is a tree, occurring in eastern Himalayas and Khasi
hills. Leaves are pinnate, leaflets 7-9, opposite, stalled, ovate-oblong. Manna
is obtained by incision from the stem of the tree and it is used as laxative
(Kritikar and Basu, 1988). The barks and leaves of the plant have been traditionally
used for the treatment of fracture and dislocation (Bijoy, 2002). The leaves
are employed as diuretic and for the treatment of gout (Anonymus, 1956). Some
coumarins have been isolated from the leaves (Nagarajan et al., 1980). The
literature survey revealed that there are no research studies carried out related
to anti-inflammatory and anti-nociceptive activities on the leaves of this
plant, hence in the present study anti-inflammatory activities in acute, sub-acute
and chronic models as well as anti-nociceptive activity by writhing test and
tail-immersion tests were determined.
Materials and Methods Collection of plant material
The leaves of Fraxinus floribunda were collected from Pakyong region
of Sikkim, India in the month of September 2005. The plant material was identified
and authenticated at Botanical Survey of India (BSI), Sikkim. A herbarium numbered
as LS/FF/04/RPS was also kept in the parent institute for future reference.
Preparation of plant extract
The collected leaves of F. floribunda was shade dried for 15 days and
reduced to coarse powder using laboratory grinder. It was stored in a well-closed
container to protect from light and moisture till used. The powdered leaves
(2.5 kg) was extracted with methanol in soxhlet apparatus. After exhaustive
extraction, the extract was concentrated in vaccuo and freeze dried
to yield a solid extract (9.2g).The dried extract was suspended in 2% Carboxy
Methyl Cellulose (CMC) and used as test drug sample for the animal studies.
Similarly, aspirin was suspended in 2% CMC and used as standard drug
Phytochemical analysis
The dried extract was subjected to phytochemical analysis for constituent identification
using standard protocol (Harborne, 1984).
Animals
Wistar Albino rats (150-200g) and Swiss Albino mice (20-35g) of either sex were
used in the studies. They were housed in large propylene cages and kept at
22±2°C in 12 h dark-light cycle. The animals were fed with rat pellet
food and water ad libitum. All animals were acclimatized for at least
one week before the experimental session. All the experimental procedures were
done following the guidelines of Institutional Animal Ethics Committee (IAEC).
Drugs and Chemicals
Aspirin, carrageenan, Freund's adjuvant were purchased from Sigma, Pentazocine
was purchased from Ranbaxy Lab Ltd, New Delhi, India. All other chemicals were
of analytical grade and procured locally.
Anti-inflammatory activity
Carrageenan induced Paw Edema (Acute Model)
Acute inflammation was produced by injecting 1% solution of carrageenan in to
plantar surface of rat hind paw at the dose of 0.1ml per 100g body weight (Winter
et al., 1963). Wistar albino rats were divided in to five groups of six in
each. A 2% solution of CMC at a dose of 0.1ml/100g/p.o was administered to
group 1. The test drug sample was administered to the animals of group 2, 3
and 4 at the dose range of 100, 200 and 400mg/kg/p.o respectively against the
standard drug aspirin at 100mg/kg/p.o to the 5. After 30 minutes carrageenan
solution was injected to the animals of all the groups. The paw edema was measured
at the intervals of 1, 2, 3 and 4h using Plethysmometer (Model-520-R,IITC Life
science, USA). The paw edema among the different group of animals was compared,
the percentage inhibition of paw edema was determined.
Vc----Paw edema of control animals
Vt----Paw edema of drug treated animals
Cotton pellet induced granuloma (Sub-acute model)
Two autoclaved cotton pellets weighing 10±1mg were implanted in both
sides of the groin region of each rat (D'Arcy et al., 1960). The animals
were divided into five groups of six each. The Control group received 2% CMC
solution at the dose of 0.1ml/100g/p.o. The test groups were treated with test
drug samples for seven consecutive days at the dose of 100, 200 and 400mg/kg/p.o.
The standard group received aspirin at the dose of 100mg/kg p.o for seven days.
After seven days animals were sacrificed by cervical dislocation and the cotton
pellets along with the granuloma tissues were dried in an oven at 60°C,
weighed and resulted weights were compared with the control. The percentage
inhibition of granuloma by the test drug was determined.
Freund's adjuvant induced arthritis (Chronic Model)
Male albino rats were divided in to five groups. On day one 0.1ml of Freund's
adjuvant was injected in to the plantar pad of each rat. The control group
received 0.1ml/100g/p.o of 2% CMC solution consecutively for 21 days. The three
test groups were treated with the test drug samples at the dose of 100, 200
and 400mg/kg/p.o for 21 days. The standard group received aspirin at 100mg/kg/p.o
for 21 days (Newbould, 1963). The paw edema of each group was measured using
Plethysmometer (Model-520-R,IITC Life sciences, USA) on day 1 before and on
day 22 after drug administration. The percentage inhibition of arthritis (Paw
edema) was calculated.
Anti-nociceptive activity
Tail-immersion test
Swiss albino mice of either sex (20-35g) were used in the study. Animals were
divided into five groups of six each. Group 1 received 0.1ml of 2%CMC solution
as control. The test drug MEFF was administered at the dose of 100, 200 and
400mg/kg p.o to the groups 2, 3 and 4 respectively against the standard drug
Pentazocine administered to group 5 at the dose of 5mg/kg i.p .The animals
were held in a suitable restrainer with tail extending out. The tail up to
5cm was then dipped into a pot of water maintained at 55±0.1ºC
(Periyanayagam et al., 2004). The time taken for the mouse to withdraw the
tail in seconds was considered as the reaction time. The reading was recorded
after 30, 60 and 120 min of administration of drugs and control.
Writhing test
Animals were divided in to five groups of six each. The control group received
0.1 ml of 2% CMC solution. The test groups were treated with 100, 200 and 400
mg/kg/p.o. of test drug samples. The standard group received aspirin at the
dose of 100mg/ kg/p.o. After 30 min of drug administration 0.7% acetic acid
was given to each mouse at the dose of 0.1 ml/10g body weight i.p. (Collier
et al.,1968). Number of writhing was counted for 15 minutes. The percentage
inhibition of writhing offered by the drug samples to the animals was calculated
and compared with the control.
Statistical analysis
The values are represented by mean±SEM; Student's t-test was performed.
P<0.05 was considered as significant.
Results
Phytochemical analysis
Phytochemical study showed that MEFF tested positive for alkaloid, steroid,
saponin and glycosides.
Anti-inflammatory activity
Carrageenan induced Paw Edema
The test drug MEFF at the dose of 100, 200 and 400 mg/kg p.o showed significant
reduction in paw edema (P<0.001) after carrageenan administration. It was
observed that MEFF at the dose of 400mg/kg /p.o produced 55.14 % percentage
inhibition of paw edema (Table-1) at the 4th hr of drug administration,
whereas, 64.48% was produced by aspirin.
Cotton pellet induced granuloma
In granuloma induced sub-acute inflammation model, the test drug MEFF at the
dose of 200 and 400 mg/kg/p.o. had significant anti-inflammatory activity (P<0.01)
(Table-2). The percentage inhibition of granuloma after drug administration
was found to be 35.72% for MEFF at the dose of 400mg/kg/p.o and 41.88% for
the standard drug aspirin.
Table 1. Anti-inflammatory activity of MEFF on carrageenan induced paw
edema in rats. Data represent mean ± SEM of 6 animals. ***P<0.001
compared to control (Student's t-test), MEFF-Methanolic Extract of leaves
of Fraxinus floribunda.
Treatment |
Paw volume in ml (% Inhibition of Paw Edema) |
|
(mg/kg/p.o.) |
1h |
2h |
3h |
4h |
Control |
1.52±0.036 |
1.84±0.061 |
2.11±0.008 |
2.14±0.073 |
MEFF-100 |
1.41±0.036*** (7.20) |
1.34±0.005*** (27.17) |
1.26±0.120*** (40.28) |
1.24±0.020*** (42.05) |
MEFF-200 |
1.32±0.004*** (13.15) |
1.25±0.017*** (32.06) |
1.10±0.034*** (42.86) |
1.08±0.025*** (51.40) |
MEFF-400 |
1.24±0.057*** (18.42) |
1.14±0.028*** (38.04) |
1.08±0.011*** (48.81) |
0.96±0.002*** (55.14) |
Aspirin-100 |
1.02±0.012*** (32.89) |
0.86±0.022*** (53.26) |
0.79±0.017*** (62.35) |
0.76±0.052*** (64.48) |
Table 2. Anti-inflammatory activity of MEFF on Cotton pellet induced
granuloma and Freund's adjuvant induced arthritis in rats. Data Represent
mean±SEM of 6 animals.*P<0.05, **P<0.01 and ***P<0.001
compared to control (student's t-test).MEFF-Methanolic Extract of leaves
of Fraxinus floribunda.
Treatment (mg/kg p.o) |
Weight of dried cotton pellet |
%Inhibition of granuloma |
Paw volume in ml |
%Inhibition of arthritis |
Control |
37.03±1.92 |
|
1.94±0.075 |
|
MEFF-100 |
31.90±0.64* |
13.86 |
1.75±0.020* |
9.79 |
MEFF-200 |
29.01±0.78** |
21.65 |
1.71±0.024** |
11.85 |
MEFF-400 |
23.80±0.77** |
35.72 |
1.67±0.013** |
13.91 |
Aspirin-100 |
21.52±0.82*** |
41.88 |
1.06±0.030*** |
45.36 |
Table 3. Antinociceptive activity of MEFF on thermally induced nociception
in mice Data represent mean±SEM of 6 animals.NS Non Significant,**P<0.01
and ***P<0.001 compared to control (student's t-test).MEFF-Methanolic
Extract of leaves of Fraxinus floribunda.
Treatment (mg/kg) |
Tail flick after 30 minutes (sec) |
Tail flick after 60 minutes(sec) |
Tail flick after 120 minutes(sec) |
Control (p.o.) |
2.78±0.451 |
2.59±0.335 |
2.43±0.314 |
MEFF -100 (p.o.) |
3.15±0.336NS |
4.18±0.456** |
4.78±0.142*** |
MEFF- 200 (p.o.) |
5.38±0.336** |
6.45±0.830** |
8.08±0.405*** |
MEFF- 400 (p.o.) |
8.54±0.356*** |
12.28±1.260*** |
13.18±0.493*** |
Pentazocine- 5 (i.p.) |
12.12±2.275*** |
14.43±0.805*** |
15.46±0.890*** |
Table 4. Antinociceptive effect of MEFF on acetic acid induced writhing
in mice. Data represent mean±SEM of 6 animals.*P<0.05,**P<0.01
and ***P<0.001 compared to control. MEFF-Methanolic Extract of
leaves of Fraxinus floribunda
Treatment(mg/kg/p.o) |
Number of writhing in 15 minutes |
% Inhibition of Writhing |
Control |
32.51±3.14 |
|
MEFF- 100 |
25.17±1.42* |
22.57 |
MEFF-200 |
22.03±1.93** |
32.23 |
MEFF- 400 |
16.62±1.84*** |
48.87 |
Aspirin -100 |
12.13±1.46*** |
62.68 |
Freund's adjuvant induced arthritis
In chronic inflammation induction model, the MEFF reduced the arthritis by 11.85%
and 16.66% at the doses of 200 and 400mg/kg/p.o. respectively compared to the
standard drug aspirin (100 mg/kg/p.o.) which reduced the arthritis by 31.28%
(Table-3).
Anti-nociceptive activity
Tail-immersion test
Tail-immersion analgesic method revealed that MEFF at all the doses significantly
delayed the time of tail withdrawal response by thermal induction of pain at
120 min (P<0.001). MEFF at the dose of 400mg/kg/p.o. showed significant
protection from nociception at 30, 60 and 120 min similar to the standard drug
pentazocine 5mg/kg i.p. (Table-3).
Writhing test
The nociception induced by 0.7% acetic acid was significantly reduced by the
MEFF in dose dependent manner (Table 4).
Discussion
Inflammatory events involve micro-vascular changes with increased vascular
permeability, flow of exudation, including plasmatic protein and amplification
of endogenous chemical mediators (Ciarino, 1998). Non Steroidal Anti-Inflammatory
Drugs (NSAIDs) are the common drugs against superficial nociception and inflammation.
NSAIDs alleviate the hyperalgesic symptoms associated with inflammation by
inhibiting the COX enzyme and the resultant inhibition of Prostaglandins synthesis
from arachidonic acid (Vane, 1971). In this study a positive step was put forward
to investigate the anti-nociceptive and anti-iflammatory actions of F. floribunda utilized
traditionally for nociception and inflammation. The methanolic extract of the
leaves of F. floribunda (MEFF) was found to have significant (P<0.001)
anti-inflammatory property in all the dose level in acute carrageenan induced
paw edema, a test which has significant predictive value for anti-inflammatory
agents acting by inhibiting the mediators of acute inflammation (Mossa et al.,
1995). In sub-acute and chronic studies, the inflammatory granuloma and arthritis
are the typical features (Olajide et al., 2000) which have been reduced significantly
(P<0.01) by MEFF at the dose level of 200 and 400mg/kg. The percentage protections
of inflammation at the dose level of 400mg/kg in acute, sub-acute and chronic
model were 55.14 (at 4th hr), 35.72 and 13.91 respectively. It provided
the feedback that MEFF was more effective in acute than sub-acute and chronic
inflammation.
The writhing induced by chemical substances is due to sensitization of nociceptors
by Prostaglandins. This test is useful for evaluation of mild analgesic non-steroidal
anti-inflammatory compounds (Ferreira and Vane, 1974).The test drug at the
dose level of 400mg/kg showed significant (P<0.001) inhibitory activity
on the writhing induced by acetic acid when compared to control. Opioid type
analgesics can be differentiated from NSAIDs by their effectiveness in the
tail-immersion test (Turner, 1965). The tail immersion results depicted that
the test drug MEFF at the dose level of 100, 200 and 400mg/kg gave significant
response (P<0.001) at 120 min. Antinociceptive study by tail-immersion test
provided the evidence for central mechanism which is also exhibited by the
test drug for relieving the pain. The studies have rationalized the ethno-medicinal
utility of the leaves of F. floribunda for various ailments related
to inflammatory disorders.
Acknowledgement
The authors are grateful to All India Council for Technical Education, New Delhi
for providing financial support in RPS (8023 RID/BOR/RPS-116/2005-2006) to
accomplish this work.
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