Antinociceptive and antipyretic activities of Amaranthus viridis Linn in different experimental models.
Methanolic extract of whole plant of Amarcinthus viridis L (MEAV), was screened for antinociceptive activity using acetic acid induced writhing test, hot plate test and tail immersion test in mice. In a similar way a screening exercise was carried out to determine the antipyretic potential of the extract using yeast induced pyrexia method in rats. Administration of the extracts was applied to both laboratory animals at the doses of 200 and 400 mg/kg body weight, respectively. The results of the statistical analysis showed that MEAV had significant (p<O.01) dose dependent antinociceptive and antipyretic properties at 200 and 400 mg/kg. Hence present investigation reveals the antinociceptive and antipyretic activities of methanolic extract of Amaranthus viridis.
Avicenna I Med Biotech 2009; 1(3): 167-171
Keywords: Analgesics, Animals, Dose response relationship, Methanol, Plant extracts
Amaranthus viridis L (A. viridis Amaranthaceae), commonly called 'Chilaka Thota-Kura' in Telugu, has been used in Indian and Nepalese traditional system to reduce labour pain and act an antipyretic (1), (2). The Negritos of the Philippines apply the bruised leaves directly to eczema, psoriasis and rashes etc (3) Other traditional uses range from an anti-inflammatory agent of the urinary tract, venereal diseases vermifuge, diuretic, antirheumatic, antiulcer, analgesic, antiemetic, laxative, improvement of appetite, antileprotic, treatment of respiratory and eye problems, to treatment of asthma (1), (4-11).
Furthermore, the plant possesses antiproliferative and antifungal lactin properties as well as ribosome inactivating protein, [beta]-carotene (12-14) and antiviral activities (15). In addition the whole plant possesses analgesic and antipyretic properties and is used for the treatment of pain and fever respectively in traditional systems of medicine (16). However, there is not enough scientific reports to support these supposed analgesic and antipyretic activities. This has prompted us to conduct the studies to ascertain the authenticity of these important claims of traditional potency.
Materials and Methods
Collection and extraction of plant material
Fresh plant material of A. viridis was collected from surroundings of Chickballapur, Karnataka in the month of May 2009. The plant material was identified and authenticated by Dr. Rajan, Department of Botany, Government Arts College, Ootcamund, Tamilnadu.
A voucher specimen (SKVCP 13) was deposited in college herbarium. Plant material was washed with water to remove dirt and shade dried for one week. The dried material was powdered by using grinder and passed through 10-mesh sieve. The coarsely powdered material was extracted with methanol by using soxhlet apparatus. The extract was later evaporated to dryness under reduced pressure and the residue was preserved for future use.
Preliminary phytochemical screening
The methanol extract of A. viridis was screened for the presence of various phytoconstituents like steroids, alkaloids, glycolsides, flavonoids, carbohydrates, proteins and phenolic compounds (17).
Male Swiss albino mice weighing 20-25 g were acclimatized to the experimental room at temperature 23[+ or -]2[degrees]C, controlled humidity conditions (50-55%) and 12 hr light and 12 hr dark cycle. A maximum of two animals were kept in a polypropylene cage and fed with standard food pellets (Kamadenu Enterprises, Bangalore) and water ad libitum.
Acute toxicity studies
Methanol extracts of A. viridis was studied for acute oral toxicity as per revised OECD (Organization for Economic Cooperation and Development) guidelines No. 423. The extract was devoid of any toxicity in rats when given in doses up to 2000 mg/kg by oral route. Hence, in our study 200 and 400 mg/kg doses of extract were dissolved in 0.1% Carboxy Methyl Cellulose (CMC) and used for the study (18).
Acetic acid-induced writhing test: This test was done using the method described by Collier et al (19). Muscle contractions were induced in mice by intra peritoneal injection of 0.6% solution of acetic acid (10 ml/kg). Thirty minutes before this administration the animals were treated with diclofenac sodium (50 mg/kg), MEAV orally at doses of (200 and 400 mg/kg) and 0.1% CMC (5 ml/kg). Immediately after administration of acetic acid, the animals were placed in glass cages, and the number of 'stretching' per animal was recorded during the following 15 min.
Writhing movement was accepted as contraction of the abdominal muscles accompanied by stretching of hind limbs. There was significant reduction in the number of writhes by drug treatments as compared to vehicle treated animals. This was considered a positive analgesic response and the percentage inhibition of writhing was calculated (19).
Hot plate met hod: The hot plate test described by Eddy and Leimback (1953) was used. The mice were first treated with different doses of MEAV (200 and 400 mg/kg orally). One hour after this administration the animals were placed on a hot plate maintained at 55[+ or -]1.0[degrees]C. A cut-off period of 15 sec was considered as maximal latency to avoid injury to the paws. The time taken by the animals to lick the hind paw or jump out of the place was taken as the reaction time and was measured at 0,30,60 and 120 mins. Morphine (5 mg/kg) was used as a reference drug (20)
Tail immersion: Tail immersion was conducted as described by Aydin et al (21). This involved immersing extreme 3cm of the rat's tail in a water bath containing water maintained at a temperature of 55[+ or -]0.5[degrees]C. Within a few minutes, the rats reacted by withdrawing the tail. The reaction time was measured at 0, 30,60,120,180,240 and 300 mins.
The test groups were given MEAV (200 and 400 mg/kg), morphine (5mg/kg) and 0.1% CMC in water were administered orally (21).
Screening for antipyretic activity
The antipyretic activity of MEAV was evaluated using Brewer's yeast-induced pyrexia in rats as described by Loux et al (22). Fever was induced by administering 20 ml/kg of 20% aqueous suspension of Brewer's yeast in normal saline subcutaneously. The MEAV (200 and 400 mg/kg, orally) was administered orally, paracetamol (150 mg/kg, orally) was used as reference drug and control group received distilled water. Rectal temperature was determined by thermal probe Eliab themistor thermometer at 1,2,3,4,5 and 6 hrs after test extract/reference drug administration (22).
Data were recorded as mean[+ or -]SEM. The statistical significance of differences between groups was determined by analysis of variance (ANOVA), followed by Dunnett's test for multiple comparisons among groups. Differences of p<O.O5 were considered statistically significant.
The present study was conducted to assess the antinociceptive and antipyretic properties of methanolic extract of A. viridis. The methods selected were chemical nociception in the test model of acetic acid-induced writhing and thermal nociception hot plate and tail immersion test. These methods were selected to evaluate both centrally and peripherally mediated effects of MEAV. The acetic acid induced abdominal constriction is believed to show the involvement of peripheral mechanisms, whereas the hot plate and tail immersion tests are believed to do same by central mechanisms (23).
The results of the present study demonstrated that MEAV-possessed antinociceptive activity is evident in all the nociceptive models, suggesting the involvement of both central and peripherally mediated activities.
In acetic acid-induced abdominal constriction test, the results showed that the MEAV (200 and 400 mg/kg) potently and significantly reduced the number of abdominal writhing in a dose dependent manner with 51.01 % and 64.73% of inhibition, respectively as compared to control animals (Table 1). The positive control group treated with diclofenac sodium (50 mg/kg) also showed significant reduction in the number of writhes (72.66%).
Table 1. Effect of methanolic extract of Amaranthus viridis (MEAV) on acetic acid induced writhing test in mice Treatment Dose (mg/kg) Number of writhes % inhibition Control -- 57.l66 [+ or -] l.66 -- Diclofenac sodium 50 15.5 [+ or -] 0.18 72.88 MEAV 200 28 [+ or -] 0.89 51.07 400 20.16 [+ or -] 0.10 64.73 Values are in mean [+ or -] SEM; (n=6)
It has been postulated that acetic acid acts indirectly by inducing the release of endogenous mediators, such as [PGE.sub.2] (prostaglandin [E.sub.2]) and [PGE.sub.2][alpha] in peritoneal fluids as well as lipooxygenase products, which stimulate the nociceptive neurons sensitive to NSAIDs (18), (24) Therefore, the results of the acetic acidinduced writhing strongly suggests that the mechanism of this extract may be linked partly to inhibition of lipooxygenase and/or cyclooxygenase in peripheral tissues, reducing in [PGE.sub.2] synthesis and interfering with the mechanism of transduction in primary afferent nociceptor (Table 1).
The central analgesic effect of the MEAV may be supported by the results recorded in the hot plate and tail immersion tests, a selective method used to screen centrally acting opiate analgesic drugs (23). It was demonstrated that oral administration of MEAV (200 and 400 mg/kg) significantly prolonged the latency time to the heat stimulus (Table 2, Figure 1).This effect began early at 30 mins after administration of MEAV and persisted until the following 120 mins. As expected, morphine (5 mg/kg) significantly increased the latency time to the nociceptive response compared with control group.
Table 2. Effect of methanolic extract of Amaranthus viridis (MEAV) on tail immersion test in mice Treatment Dose Post reaction treatment (mg/kg) 0 min 30 min 60 min 120 min Control 2.31 [+ 2.48 [+ 2.43 [+ or 2.31 [+ or or -] or -] -] 0.09 -] 0.056 0.08 0.07 Morphine 5 2.45 [+ 6.0 [+ 7.8 [+ or -] 9.8 [+ or or -] or -] 0.13 ** -] 0.19 ** 0.095 0.15 ** MEAV 200 2.45 [+ 4.62 [+ 6.0 [+ or -] 6.2 [+ or or -] or -] 0.07 ** -] 0.07 ** 0.12 0.17 * 400 2.33 [+ 5.23 [+ 7.48 [+ or 8.05 [+ or or -] or -] -]0.12 ** -] 0.14 ** 0.06 0.12 ** Treatment Time (seconds) 180 min 240 300 min min Control 2.34 [+ or 2.3 [+ 2.3 [+ -] 0.06 or -] or -] 0.03 0.06 Morphine 8.2 [+ or -] 3.8 [+ 3 [+ or 0.15 ** or -] -] 0.06 0.014 ** MEAV 5.6 [+ or -] 2.8 [+ 2.4 [+ 0.148 ** or -] or -] 0.12 * 0.15 5.7 [+ or -] 3.14 [+ 2.67 [+ 0.15 ** or -] or -] 0.08 0.08 ** Values an in mean [+ or -] SEM; (n=6) *P<0.05, ** n<0.01 vs control
[FIGURE 1 OMITTED]
Fever may be a result of infection or one of the sequelae of tissue damage, inflammation, graft rejection, or other disease states. Antipyretics are drugs, which reduce the elevated body temperature. Regulation of body temperature requires a delicate balance between production and loss of heat, and the hypothalamus regulates the set point at which body temperature is maintained. In fever this set point elevates and a drug like paracetamol does not influence body temperature when it is elevated by the factors such as exercise or increase in ambient temperature (25).
The results obtained (Table 3) revealed that MEAV showed significant (p<O.O5) antipyretic activity at all doses tested. The MEAV at 400 mg/kg showed antipyretic activity after 19 hrs of administration of Brewer's yeast and continued until the end of the experiment, while 200 mg/kg dose showed reduction in temperature after 22 hrs of administration of Brewer's yeast extending up to 23 hrs. Therefore, the MEAV possesses a significant antipyretic effect in yeast-induced elevation of body temperature in rats and this may be attributed to the anti-inflammatory properties of the plant.
Table 3. Effect of methanolic extract of Amaranthw viridis (MEAV) on yeast induced pyrexia Treatment Dose Rectal temperature ([degrees]C) (mg/kg) Ohr 19hr 20hr 21hr Control 37.39 [+ 39.16 [+ 39.2 [+ or 39.2 [+ or -] or -] or -] -] 0.15 0.15 0.03 0.02 Paracetamol 150 36.93 [+ 38.6 [+ 37.33 [+ 37.33 [+ or -] or -] or -] or -] 0.21 0.31 ** 0.41 0.56 ** MEAV 200 37.26 [+ 39.1 [+ 38.5 [+ or 38.35 [+ or -] or -] or -] -] 0.34 0.335 * 0.17 0.18 400 37.4 [+ 38.78 [+ 37.86 [+ 37.63 [+ or or -] or -] or -] 0.42 -]0.22 ** 0.17 0.45 * Treatment after yeast injection 22/hr 23hr 24hr Control 39.2 [+ or -] 39.05 [+ 38.58 [+ 0.15 or -] or -] 0.18 0.21 Paracetamol 37.52 [+ or 37.41 [+ 37.26 [+ -] 0.17 ** or -] 0.2 or -] ** 0.16 ** MEAV 38.28 [+ or 38.12 [+ 38.1 [+ -] 0.17 * or -] or -] 0.21 * 0.106 37.45 [+ or 37.57 [+ 37.4 [+ -] 0.19 ** or -] or -] 0.20 ** 0.17 ** Values are in mean [+ or -] SEM; (n=6) *p<0.05, ** p<0.01 vs control
Preliminary phytochemical study indicated the presence of alkaloids, steroids, glycosides, flavonoids, phenolic compounds, terpenoids, proteins and carbohydrates which might be responsible for the antinociceptive and antipyretic effects of the MEAV.
Flavonoids and phenolic compounds have been reported to have multiple biological effects such as anti-oxidant activity (26), antinociceptive activity in vivo (27), (28), anti inflammatory action (29), (30) inhibition of platelet aggregation (31), inhibition of mast cell histamine release (32) and inhibitory action on arachidonic acid metabolism as demonstrated by in vitro and in vivo tests (33).
The authors wish to thank Sri K.V. Naveen Kiran, Chairman, Sri K.V. College of Pharmacy, Chickballapur, Kamataka (India), for providing the research facilities to carry out this work successfully.
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* Corresponding Author:
Ashok Kumar, B.S.,M. Pharm (Ph.D.), Department of Pharmacognosy, Sri K.V.College of Pharmacy, Chickballapur, Karnataka, India
Received: 28 Oct 2009
Accepted: 1 Dec 2009
Bagepalli Srinivas Ashok Kumar(1) *, Kuruba Lakshman(2), Korala Konta Narsimha Jayaveera(3), Devangam Sheshadri Shebar(4), Chinna SwamyVel Muragan(4), and Bachappa Manoj(1)
(1.) Department of Pharmacognosy, Sri K.V. College of Pharmacy, Chickbcziapur, Kamataka, India
(2.) Department of Pharmacognosy, PES College of Pharmacy, Bangalore, Kornataka, India
(3.) Department of Chemistry, Jawaharlal Nehru Technological University of College of Engineering, Ancintapur, Andhra Pradesh, India
(4.) Department of Pharmacology, Sri K.V. College of Pharmacy, Chickballapur, Kamataka, India
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|Title Annotation:||Original Article|
|Author:||Kumar, Bagepalli Srinivas Ashok; Labshman, Kuruba; Narsimha Jayaveera, Korala Konta; Shebar, Devanga|
|Publication:||Avicenna Journal of Medical Biotechnology (AJMB)|
|Date:||Oct 1, 2009|
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