Antinociceptive and Anti-inflammatory Properties of Melastoma malabathricum Leaves Chloroform Extract in Experimental Animals
R.N.S. Raden Mohd Nor,
Z.D.F. Abdul Ghani,
G. Hanan Kumar
The present study was carried out to establish the antinociceptive, anti-inflammatory and antipyretic properties of Melastoma malabathricum leaves chloroform extract in experimental animals. The antinociceptive activity was measured using the abdominal constriction, hot plate and formalin tests, while the anti-inflammatory was measured using the carrageenan-induced paw edema. The extract, obtained after 72 h soaking of the air-dried leaves in chloroform followed by evaporation under vacuo (40°C) to dryness (4.38 g), was dissolved in dimethyl sulfoxide to the doses of 20, 100 and 200% and administered subcutaneously 30 min prior to subjection to the above mentioned assays. The extract, at all concentration used, was found to exhibit significant (p<0.05) antinociceptive and anti-inflammatory activities. Only the effect observed with the formalin test occurred in a concentration-dependent manner. It is concluded that the lipid-soluble compounds within the chloroform extract of M. malabathricum leaves possess potential antinociceptive and anti-inflammatory agents that require further attention.
to cite this article:
Z.A. Zakaria, R.N.S. Raden Mohd Nor, M.R. Sulaiman, Z.D.F. Abdul Ghani, G. Hanan Kumar and C.A. Fatimah, 2006. Antinociceptive and Anti-inflammatory Properties of Melastoma malabathricum Leaves Chloroform Extract in Experimental Animals. Journal of Pharmacology and Toxicology, 1: 337-345.
Melastoma malabathricum, a plant that belongs to the family Melastomataceae, is a common shrub found in previously cleared land and waste places (Burkill, 1966). The plant, also known to the Malays as Senduduk, has been used in the traditional medicine to treat various types of ailments (Jaganath and Ng, 2000). For examples, the chewed or pounded leaves of M. calabura, were pasted onto the inflamed wound while juices of the finely chopped leaves were squeeze onto the inflamed wound to stop bleeding (Ahmad et al., 1993). In addition, Jaganath and Ng (2000) have also reported the use of the powdered leaves of M. malabathricum as an astringent for dysentery or to alleviate the discomfort of hemorrhoids while the Institute of Medical Research (2002) have also listed the leaves application onto wounds and pox scars to enhance the healing process. Other than that the liquid obtained after boiling the leaves can be use to treat diarrhea (Institute of Medical Research, 2002). However, all of the claims above have never been scientifically proven. Recent scientific study by Sulaiman et al. (2004) has revealed the potential of the ethanolic extract of M. malabathricum leaves as an antinociceptive agent that act at the peripheral and central levels. Opioid receptors have also been shown to take part in the reported activity of the extract. Although there is claim on the presence of compounds like quercetin, quercitrin, rutin, β-sitosterol, α-amyrin and sitosterol 3-O-β-D-glucopyranoside in the plant (Sulaiman et al., 2004) there is no scientific publication to confirm that finding.
Despite the fact that the M. malabathricum is famously used in the Malays traditional culture to treat various ailments and due to the lack of scientific study to establish the its pharmacological potentials, the present study was carried out to evaluate the antinociceptive and anti-inflammatory properties of the lipid-soluble compounds of M. malabathricum leaves obtained through chloroform extraction.
Materials and Methods
M. malabathricum were collected in August-September, 2005 from its
natural habitat in Shah Alam, Selangor, Malaysia. It was identified by Mr. Shamsul
Khamis, a botanist at the Institute of Bioscience, Universiti Putra Malaysia,
Serdang, Selangor, Malaysia and a voucher specimen (SK 507/03) was deposited
at the Herbarium of the Laboratory of Natural Products, IBS, UPM, Malaysia.
Phytochemical Screening of the M. malabathricum Leaves
The phytochemical screening of C. malabathricum leaves was carried
out according to the standard screening tests and conventional protocols as
described by Ikhiri et al. (1992).
Preparation of Chloroform Extract of M. malabathricum (CEMM)
The CEMM was prepared by soaking the air-dried powdered leaves of M.
malabathricum (20 mg) in chloroform in the ratio of 1: 20 (w/v) for 72 h.
The supernatant was collected and filtered using Whatman No. 1 filter paper
while the remaining plant residue was discarded. The filtered supernatant obtained
was evaporated to dryness and the weight of the crude dried chloroform extract
obtained was measured (4.38 g). The dried extract was diluted in Dimethyl Sul
Foxide (DMSO) (1:50; w/v) and considered as the stock solution with 100% concentration/strength.
The stock solution was diluted again with DMSO to the concentrations of 10 and
50% for the antinociceptive and anti-inflammatory studies. Simple calculation
has demonstrated that the 10, 50 and 100% concentrations CEMM were approximately
equal to the doses of 20, 100 and 200 mg kg-1, respectively.
Preparation of Drugs
Hundred mg kg-1 AcetylsAlicylic Acid (ASA) (Bayer, Singapore)
and 5 mg kg-1 morphine (Sigma, Germany), used for the purposed of
comparison, were prepared by dissolving them in dH2O.
Male Balb-C mice (25-30 g; 5-7 weeks) and Sprague-Dawley rats (180-200 g;
8-10 weeks old), obtained from the Animal Source Unit, Faculty of Veterinary
Medicine, Universiti Putra Malaysia (UPM), Serdang, Selangor, Malaysia, were
used in this study. All of the animals were kept under room temperature (27±2°C;
70-80% humidity; 12 h light/darkness cycle) in the Animal Holding Unit, Faculty
of Medical and Health Sciences, UPM for at least 48 h before use. Food and water
were supplied ad libitum up to the beginning of the experiments. At all
times the mice and rats were cared for in accordance with current UPM principles
and guidelines for the care of laboratory animals and the UPM ethical guidelines
for investigations of experimental pain in conscious animals as adopted from
All mice were equally divided into 10 groups of 7 mice each (n = 7) and received (sc) DH2O, ASA (100 mg kg-1) or CEMM (10, 50 and 100% strength) 30 min prior to subjection to the abdominal constriction or hot plate tests, respectively. On the other hand, all rats were equally divided into 11 groups of 5 rats each (n = 5). The first six groups were used in the formalin test and received (sc) dH2O, 100 mg kg-1 ASA, 5 mg kg-1 morphine or CEMM (10, 50 and 100% concentrations), respectively 30 min prior to subjection to the test. The second five groups were used in the anti-inflammatory study and received (sc) dH2O, 100 mg kg-1 ASA or CEMM (10, 50 and 100% concentration), respectively 30 min prior to subjection to the test. All of the test solutions were administered in the volume of 10 mL kg-1 body weight.
Abdominal Constriction Test
The abdominal constriction test (Dambisya and Lee, 1995) with slight modification
as described by Zakaria et al. (2005) was used to evaluate the chemically-induced
antinociceptive activity of CEMM.
Hot Plate Test
The 50°C hot-plate test (Wilson et al., 2003) with slight modification
as described by Zakaria et al. (2005) was used to evaluate the thermally-induced
central antinociceptive activity of CEMM.
The formalin test described by Hunskaar and Hole (1987) was used but with
slight modifications. Pain was induced by injecting 50 μL of 5% formalin
in the subplantar region of the left hind paw. Rats were given (sc) test solutions
30 min prior to formalin injection. The rats were individually placed in transparent
Plexiglass cage observation chamber. The amount of time the animal spent licking
the injected paw (Mendes et al., 2000), considered as an indicator of
pain, was recorded for duration of 30 min following the formalin injection.
The early phase of nociception, indicating a neurogenic type of pain response,
was measured between 0-5 min while the late phase of nociception, indicating
an inflammatory type of pain response, was measured 15-30 min after formalin
The carrageenan-induced paw edema test (Chakraborty et al., 2004)
with slight modification as described by Zakaria et al. (2006) was used
to determine the anti-inflammatory activity of CEMM.
The results are presented as Mean±Standard Error of Mean (SEM). The
one-way ANOVA test with Dunnett post-hoc test was used to analyze and compare
the data, with p<0.05 as the limit of significance.
Phytochemical Screening of the M. malabathricum Leaves
The phytochemical screening of the leaves of M. malabathricum has
demonstrated the present of flavonoids, saponins, tannins, steroids and triterpenes
but no alkaloids.
Pharmacological Studies on the CEMM
Figure 1 shows the antinociceptive profile of CEMM assessed
using the acetic acid-induced adominal constriction test in mice. The extract,
at all concentrations used, exhibited a significant (p<0.05) antinociceptive
activity in a concentration-independent manner.
||The antinociceptive profile of CEMM assessed by the abdominal
constriction test in mice.
*Significant (p<0.05) when compared to the control group
|| The antinociceptive profile of CEMM assessed by the hot plate
test in mice
The 50% concentration CEMM produced a more effective activity than that of
the 100% concentration CEMM when compared to the control group with the former
caused approximately 6 folds decrease in the number of abdominal constriction
while the latter caused only 2 folds decrease. The 10 and 100% concentrations
CEMM produced an equi-effective activity when compared to the 100 mg kg-1
The antinociceptive profile of CEMM assessed using the hot plate test in mice was shown in Fig. 2. The CEMM, at all concentrations used, also exhibited a significant (p<0.05) antinociceptive activity in a concentration-independent manner. The 10% concentration CEMM was found to produce constant antinociceptive activity throughout the experimental time while the other two concentrations showed somewhat inconsistence activity between the interval 1-2 h. The 50% concentration CEMM lost its activity at the interval time of 1 h while the 100% concentration CEMM lost its activity at the interval time of 2 h after their administration. Interestingly, the activity of both concentrations of the extract were found to increase significantly (p<0.05) after that and maintained until the end of the experiment. Throughout the study, the 5 mg kg-1 morphine antinociceptive activity was found to be greater than that of the extract except at the last interval time (5 h ) where its activity was significantly (p<0.05) lower than the 50% concentration CEMM.
||The antinociceptive profile of CEMM assessed by the formalin
test in rats.
* Significant (p<0.05) when compared to the respective control group
||The anti-inflammatory profile of AEMM assessed by the carrageenan-induced
paw edema test in rats
The antinociceptive profile of CEMM assessed using the formalin test in rats was shown in Fig. 3. The extract, at all concentrations used, exhibited significant (p<0.05) antinociception in both phases of nociception with a more effective activity seen in the late phase. The extract was found to block the early phase nociception only at the highest concentration used whereas the inhibition of the late phase was observed in all of the concentrations used. Interestingly, the 100% concentration CEMM caused almost complete and complete inhibition of the nociception in the early and late phases, respectively.
The anti-inflammatory profile of CEMM assessed using the carrageenan-induced paw edema test in rats can be seen in Fig. 4. The CEMM exhibited significant (p<0.05) activity at all of the concentrations used but in a concentration-independent manner. The activity can be seen as early as 1 h after the extract administration and lasted for the first 6 h. Except for the 50% concentration CEMM which still maintained its significant (p<0.05) activity, the other concentrations of CEMM were found to lost their anti-inflammatory activity. Except at the interval time of 4 h where it lost the activity, the 100 mg kg-1 ASA was found to produce significant (p<0.05) anti-inflammatory for the first 6 h before the activity diminished for the next 2 h. Throughout the experimental time, the 100 mg kg-1 ASA anti-inflammatory activity was found to be lower than that of the extract.
The present study demonstrated the ability of CEMM to produce the antinociceptive and anti-inflammatory activities in experimental animals. The ability to produce antinociceptive activity in those assays indirectly indicates the extract ability to inhibit chemically-and thermally-induced nociception. According to Hunskaar et al. (1986) and Hunskaar and Hole (1987) the ability to inhibit both types of nociceptive stimulus indicate the extracts characteristic as strong analgesics such as opioid agonists (morphine).
In addition, the ability to prolonged latency to discomfort/pain in the hot plate test coupled with the reversed of early phase nocicpetion seen in the formalin test indicates the extract antinociceptive activity involved central mechanism (Pini et al., 1997; Amanlou et al., 2005). According to Hosseinzadeh and Younesi (2002), the ability to inhibit both types of tests, the abdominal constriction and hot plate tests, also suggested that the extract possessed a centrally mediated activity. Although the exact mechanism of antinociceptive action of the CEMM is not yet determined, it is plausible to suggest the involvement of opioid receptor (Sulaiman et al., 2004) as part of the mechanism involved. The involvement of Cyclo-Oxygenase (COX) in the central antinociceptive mechanism of the CEMM is also worth mentioned based on the earlier report made by Pini et al. (1997) on the paracetamol-induced central antinociceptive activity involved the central COX inhibition and the later report by Ballou et al. (2000) on the present of central COX, which also contributes to the central nociceptive processes.
Other than that, the abilities to block the late phase nociception as well as to reverse the edema formation in the carrageenan-induced paw edema test suggested that the CEMM-mediated antinociceptive activity particularly involved, in part, inhibition of the COX action or prostaglandin synthesis (Amanlou et al., 2000; Damas et al., 1986). According to Damas et al. (1986), the edema development could be attributed to the presence of kinins and polymorphonuclear leucocytes, which have been associated with the release of pro-inflammatory mediators like prostaglandins. This suggestion is supported by finding made Ballou et al. (2000) that the abdominal constrictions induced by the acetic acid were due to the release of COX-synthesized prostacyclin within the peritoneal cavity.
The abdominal constriction test, although was very sensitive in detecting an antinociceptive property of compounds/dose levels that may be inactive in other tests (Bentley et al., 1981), is not specific because it could no be use to specify the involvement of peripheral and/or central mechanism in the observed antinociceptive activity of compounds/CEMM (Chan et al., 1995). It has been demonstrated that the acetic acid-induced irritation of the peritoneal cavity (Deraedt et al., 1980) caused stimulation of the local receptors located at the surface of the cells lining the peritoneal cavity (Bentley et al., 1983), which in turn caused release of prostaglandins, particularly the PGE2 and PGE2α, that lead to inflammatory pain (Vogel and Vogel, 1997). Due to its inability to specify the actual mechanism that take part in the CEMM antinociceptive activity, additional studies using the hot plate and formalin assays have to be carried out before a final conclusion could be draw on the actual mechanism involved in the extract antinociceptive activity.
The hot plate test has been regarded as one of the best methods to study on the central antinociceptive effect of a compound/extract (Pini et al., 1997). The thermal stimulus is also described as acute, non-inflammatory nociceptive stimulus as it caused direct stimulation of the nociceptors without causing any inflammatory-mediated nociception. Centrally, but not peripherally, acting drugs increased the latency to discomfort (Hosseinzadeh and Younesi, 2002; Amanlou et al., 2005) and this activity is also observed with the CEMM indicating that the extract also possessed centrally-mediated action.
The formalin test, usually used to study the non-anti-inflammatory, antinociceptive
properties of a compound/extract (Hunskaar et al., 1985), produces a
distinct biphasic nociceptive response described as the early and late phases.
The early phase, caused by a direct effect of formalin on nociceptors and does
not involved the inflammatory process, occurred almost immediately following
the formalin administration and continues for 5 min while the late phase, involved
the inflammatory process and activation of the neurons located in the dorsal
horns of the spinal cord, can be seen between 15 and 60 min after the formalin
administration (Tjølsen et al., 1991). According to Chan et
al. (1995), drugs acting centrally affect both phases while those acting
peripherally were effective only in the late phase of the formalin test. Therefore,
the ability of CEMM to affect both phases of the formalin test indicates its
potential central antinociceptive mechanism (Chan et al., 1995) and confirmed
the earlier observation using the hot plate test.
Carrageenan-induced rat paw edema test has been accepted as one of the methods to screen for new anti-inflammatory compounds/extracts (Chan et al., 1995; Joseph et al., 2005; Di Meglio et al., 2005). The development of edema has been associated with the presence of kinins and polymorphonuclear leucocytes, with the latter demonstrated to release pro-inflammatory factors, particularly prostaglandins. Thus, the edema reducing ability of CEMM could be attributed to the extract ability to inhibit prostaglandin release or COX-mediated prostaglandin synthesis (Damas et al., 1986).
Except for the antinociceptive effect assessed using the formalin test, the rest of the effects occur in a concentration-independent manner. The 100% concentration CEMM activity was less effective than the other extract might be associated with the phenomenon known as therapeutic windows (Tripathi, 2001) or receptor deactivation (Katzung, 1995). Certain drugs have been demonstrated to exhibit desired therapeutic effects only over a narrow range of doses or plasma drug concentrations and suboptimal beneficial activities or even decline in activities would be produced if the dose used were below or above the narrow therapeutic range (Tripathi, 2001). On the other hand, certain drugs have been reported to cause deactivation of the receptor when presence at high concentration within the biological system (Katzung, 1995). However, further studies need to be carried out before we could clarify on those phenomenon involvements in the mechanism of action of CEMM.
Based on the findings, it is plausible to suggest that lipid-soluble/non-polar compounds could also take part in the observed activities as chloroform is an organic solvent that dissolved lipid-soluble compounds (Vogel et al., 1989). Some compounds, such as those of flavonoid types, have been reported to be isolated through chloroform extraction (Chen et al., 2005). Other than the flavonoids, tannins have also been isolated from the leaves of M. malabathricum (Yoshida et al., 1992a; Lohézic-Le Dévéhat et al., 2002). Flavonoids, in particular, have been demonstrated to possess an anti-inflammatory activity (Kim et al., 2004). Our observations on the antinociceptive and anti-inflammatory activities of CEMM are concurrent with claimed made Attaway and Zaborksy (1993). Finally, it is concludes that the CEMM possessed an antinociceptive, which is mediated via peripheral and central mechanismsand anti-inflammatory activities and justify the folklore uses of the plant in treating ailments associated with pain and inflammation.
This study was supported by the research grant of Universiti Industri Selangor, Malaysia (Project Code Number: 03013; Project Vote Number: 3090103013). The authors would like to thanks Universiti Putra Malaysia for some of the facilities.
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