PHARMACOGNOSY
Year : 2009  |  Volume : 1  |  Issue : 4  |  Page : 322-325 Table of Contents     

Antihistaminic effect of various extracts of Punica granatum Linn. flower buds


1 Department of Pharmacognosy, Pravara Rural College of Pharmacy, Loni, M.S, India
2 Department ofPharmacognosy, NDMVP College of Pharmacy, Nashik, M.S, India
3 Pharmacognosy and Phytochemistry Research Laboratory, Department of Pharmaceutical Technology, Jadavpur University, Kolkata, India

Date of Web Publication25-Jan-2010

Correspondence Address:
A Nirmal Sunil
Department of Pharmacognosy, Pravara Rural College of Pharmacy, Loni, M.S
India
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DOI: 10.4103/0975-1483.59321

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   Abstract 

Punica granatum Linn. (Punicaceae) flower buds are used in the treatment of asthma traditionally, so the present work was undertaken to prove it scientifically using suitable animal models. Antihistaminic principles are useful in the treatment of asthma,;hence, in present work antihistaminic activity of various extracts of P. granatum flower buds was checked using clonidine-induced catalepsy and haloperidol-induced catalepsy in Swiss albino mice at the dose of 50 and 100 mg/kg, p.o. The results showed that ethanol extracts (100 mg/kg, p.o.) are having significant antihistaminic activity amongst other extracts. Thus, it can be concluded that tannins from the flower buds of P. granatum may be responsible for antihistaminic activity and may have potential role in the treatment of asthma.

Keywords: Antihistaminic, catalepsy, clonidine, haloperidol, Punica granatum


How to cite this article:
Barwal S B, Sunil A N, Dhasade V V, Patil M J, Pal S C, Subhash C M. Antihistaminic effect of various extracts of Punica granatum Linn. flower buds. J Young Pharmacists 2009;1:322-5

How to cite this URL:
Barwal S B, Sunil A N, Dhasade V V, Patil M J, Pal S C, Subhash C M. Antihistaminic effect of various extracts of Punica granatum Linn. flower buds. J Young Pharmacists [serial online] 2009 [cited 2013 Apr 20];1:322-5. Available from: /text.asp?2009/1/4/322/59321


   Introduction Top


Punica granatum Linn. (Punicaceae) tree iscultivated all over in India. The various parts root, bark, leaves, fruit, and flower buds are used in traditional medicine for treatment of asthma, diarrhea, dysentery, tuberculosis, antidotes for snakebite, and as anthelmintic and astringent. [1] The plant has antioxidant, [2] antiallergic, [3] antimicrobial, [4] antiplasmodial, [5] antidiabetic, [6] hepatoprotective, [7] and anticancer [8] activities. Catalepsy is a condition in which the animal maintains imposed posture for long time before regaining normal posture. Catalepsy is a sign of extra-pyramidal effect of drugs that inhibit dopaminergic transmission or increase histamine release in brain. Clonidine, a α2 -adrenoceptor agonist, induces dose-dependent catalepsy in mice, which is inhibited by histamine H 1 receptor antagonists but not by H 2 receptor antagonist. [9] They also showed that pretreatment with L-histidine, a precursor of histamine-potentiated clonidine-induced catalepsy in a dose dependent manner. Muley et al., (1979) showed that intracerebroventricular injection of histamine in conscious mice induced catalepsy, which was inhibited by H 1 receptor antagonist but not by H 2 receptor antagonist. [10] i0 t is known that clonidine releases histamine from mast cells. [11] Schwatz (1997) identified histamine-containing mast cells in brain. [12] Clonidine-induced release of histamine from mast cells is inhibited by α2 -adrenoceptor blocker, prazocine. [13] Neuroleptic agent also induced catalepsy, but by a different mechanism. Neuroleptic agents inhibit dopamine D 2 receptor in the substantia nigra. [14],[15] Therefore, it was our objective to study the effect various extracts of P. granatum flower buds on clonidine-induced catalepsy, as it is used traditionally in the treatment of asthma. [16] Since catalepsy is a common extra-pyramidal side effect of neuroleptic agents and the effect of the plant on haloperidol-induced catalepsy is not known, we also studied their effect on haloperidol-induced catalepsy in mice.


   Materials and Methods Top


Plant material

Fresh flower buds of P. granatum was collected from Ahmednagar district and authenticated by Mr. S.C. Mujumdar, Deputy Director, Botanical survey of India, Koregaon Road, Pune. The herbarium of plant specimen has been deposited at B.S.I. Pune, the voucher no. BSBP1, vide letter no. BSI/WC/Tech/2007/795, dated 20 th November 2007.

Extraction

Dried and coarsely powdered flower buds of P. granatum were subjected to successive solvent extraction in Soxhlet extractor using petroleum ether, chloroform, and ethanol as solvent, and the marc left was refluxed with water. All the extracts were vacuum dried to produce PEE (7.3%), CLE (5.5%), EE (56%),, and AQE (16%) respectively.

Animals

Male albino mice (Swiss strain) weighing 22-25 g were housed under standard laboratory conditions, in groups of six each. The animal had free access to food and water. The ethical committee of the institute approved the protocol of the study.

Drugs and Chemicals

The following drugs and chemicals were used. Drugs: clonidine (Unichem, India), haloperidol (Sunpharma, India.), pheniramine maleate (Pfizer Ltd.) purchased from commercial source. Chemicals: petroleum ether AR (60-80 0 c) (PCL, India), chloroform AR (PCL, India), ethanol AR (PCL, India), and Tween 80 AR (PCL, India).

Preliminary phytochemical study

The preliminary phytochemical study of various extracts of P. granatum was performed as per Khandelwal. [17]

Effect on clonidine-induced catalepsy

The bar test was used to study the effect of various extracts on clonidine-induced catalepsy. [18] Clonidine (1 mg/kg, s.c.) was injected to mice (n=6) pretreated 60 min before with vehicle (Tween 80 in distilled water) (5 ml/kg, p.o.), petroleum ether, ethyl acetate, ethanol, and aqueous extracts of P. granatum (50 and 100 mg/kg, p.o., each) or standard drug pheniramine maleate (10 mg/kg, i.p.). t0 he dosages were selected based on acute toxicity studies (data not shown). The forepaws of mice were placed on horizontal bar (1 cm in diameter, 3 cm above the table) and the time required to remove the paws from bar was noted for each animal and the duration of catalepsy was measured at 0, 15, 30, 60, 90, 120, 150, and 180 min.

Effect on haloperidol-induced catalepsy

The same Bar test was used using haloperidol. [18] Haloperidol (1 mg/kg, i.p.) was injected to mice (n=6) pretreated 60 min before with vehicle (Tween 80 in distilled water) (5 ml/kg, p.o.), petroleum ether, ethyl acetate, ethanol, and aqueous extracts of P. granatum (50 and 100 mg/kg, p.o., each). The duration of catalepsy was measured at 0, 15, 30, 60, 90, 120, 150, and 180 min.

Statistical analysis of data

Data are presented as mean ± SEM. Statistical comparison between groups were analyzed by one-way analysis of variance (ANOVA) followed by Dunnet's test. Prism Graph pad 3 was used for statistical analysis. **P<0.001, *P< 0.05, compared with the control group.


   Results Top


Preliminary phytochemical study

The ethanol extract of P. granatum flower buds showed the presence of tannins.

Clonidine-induced catalepsy

The result showed that ethanol extract significantly inhibited clonidine-induced catalepsy than other extracts. The results are compared with pheniramine maleate. Other extract were found to be non-significant [Table 1].

Haloperidol-induced catalepsy

None of the extracts inhibited haloperidol-induced catalepsy [Table 2].


   Discussion Top


Several drugs are known to induce catalepsy in animals. The neuroleptic agents induce catalepsy by inducing dopamine D 2 receptor in the substantia nigra. [14] Chopra and Dandiya (1975) have studied the relative role of acetylcholine and histamine in perphenazine-induce catalepsy and suggested that anticholinergic activity of antidepressant might be due to an increase in dopamine content in brain or their ability to inhibit release of acetylcholine. [19] They also showed that different stages of catalepsy appear to be directly correlated with brain histamine content. Uvnas (1969) studied the mast cell degranulation and its correlation with the release of histamine after administration of mast cell degranulating agent (Compound 48/80). [20] Lakdawala et al. (1980) have shown that clonidine releases histamine from mast cell in a similar manner to a selective liberator like compound 48/80. [11]

The observation of this study indicated that the ethanol and aqueous extract s of P. granatum flower buds inhibited clonidine-induced catalepsy and not inhibited haloperidol-induced catalepsy. From the present study, we can conclude that the cataleptic effect of clonidine in the mouse is mediated by histamine release from mast cells and the clonidine-induced catalepsy was inhibited by ethanol extract of P. granatum flower buds. The effect of these extracts on clonidine-induced catalepsy is probably due to their mast cell-stabilizing property, and the plant does not have activity on dopaminergic transmission. So it can be concluded that ethanol extract containing tannins may be responsible for antihistaminic activity and may be used in the treatment of asthma.

 
   References Top

1.Nadkarni KM. Indian materia medica. 3 rd ed. Vol. 1. Bombay: Bombay Popular Prakashan; 1982: p. 1031-3.  Back to cited text no. 1      
2.Elfalleh W, Nasri N, Marzougui N, Thabti I, M'rabet A, Yahya Y, Lachiheb B, Guasmi F, Ferchichi A. Physico-chemical properties and DPPH-ABTS scavenging activity of some local pomegranate (Punica granatum) ecotypes. Int J Food Sci Nutr 2009;60:197-210.  Back to cited text no. 2      
3.Damiani E, Aloia AM, Priore MG, Nardulli S, Ferrannini A. Pomegranate (Punica granatum) allergy: clinical and immunological findings. Ann Allergy Asthma Immunol 2009;103:178-80.  Back to cited text no. 3      
4.Al-Zoreky NS. Antimicrobial activity of pomegranate (Punica granatum L.) fruit peels. Int J Food Microbiol 2009;134:244-8.  Back to cited text no. 4      
5.Dell'Agli M, Galli GV, Corbett Y, Taramelli D, Lucantoni L, Habluetzel A, Maschi O, Caruso D, Giavarini F, Romeo S, Bhattacharya D, Bosisio E. Antiplasmodial activity of Punica granatum L. fruit rind. J Ethnopharmacol 2009;125:279-85.  Back to cited text no. 5      
6. McFarlin BK, Strohacker KA, Kueht ML. Pomegranate seed oil consumption during a period of high-fat feeding reduces weight gain and reduces type 2 diabetes risk in CD-1 mice. Br J Nutr 2009;102:54-9.  Back to cited text no. 6      
7.Celik I, Temur A, Isik I. Hepatoprotective role and antioxidant capacity of pomegranate (Punica granatum) flowers infusion against trichloroacetic acid-exposed in rats. Food Chem Toxicol 2009;47:145-9.   Back to cited text no. 7      
8.Khan SA. The role of pomegranate (Punica granatum L.) in colon cancer. Pak J Pharm Sci 2009;22:346-8.   Back to cited text no. 8      
9.Jadhav JH, Balsara JJ, Chandorkar AG. I0 nvolvement of histaminergic mechanism in the cataleptogenic effect of clonidine in mice. Pharm Pharmacol 1983;35:671- 3.  Back to cited text no. 9      
10.Mulay MP, Balsara JJ, Chandorkar AG. Intracerebroventricular administration of histamine in conscious mice during catalepsy. Ind Pharmac 1979;11:277-81.  Back to cited text no. 10      
11.Lakadwala AD, Dadkar NK, Dohadwala AN. Action of clonidine on mast cells of rats. Pharm Pharmacol 1980;32:790-3.  Back to cited text no. 11      
12.Schwartz JC. Annual review of Pharmacology and Toxicology. In: Elliot HW, George R, Okun R, editors. Palo Alto: Ann Reviews Inc; 1997. p. 325-39.  Back to cited text no. 12      
13.Weiner N. Drugs that inhibit adrenergic nerves and block adrenergic receptors. In: Gilman AG, Goodman LS, editors. The Pharmacological Basis of Therapeutics. 7 th ed. New York: Macmillan Publishing co.; 1985. p. 176-210.  Back to cited text no. 13      
14.Sanberg PR. Haloperidol induced catalepsy is mediated by postsynaptic dopamine receptor. Nature 1980;284:472-3.  Back to cited text no. 14      
15.Ossowska K, Karcz M, Wardas J. Straiatal and nucleus accumbens D 1 /D 2 dopamine receptor in neuroleptic catalepsy. Eur J Pharmac 1990;182:327-34.  Back to cited text no. 15      
16.Kirtikar KR, Basu BD. Indian Medicinal Plants. 2 nd ed. Vol. 3. Dehradun: Bishen Singh Mahendra Pal Singh; 1991: p. 667-70.  Back to cited text no. 16      
17.Khandelwal KR. Practical Pharmacognosy Technique and Experiments. 23 rd ed. Pune: Nirali Prakashan; 2005: p. 15-29, 149-56.  Back to cited text no. 17      
18.Ferre S, Guix T. Prat G. Is experimental catalepsy properly measured? Pharmac Biochem Behav 1990;35:753-7.  Back to cited text no. 18      
19.Chopra YM, Dandiya PC. The relative role of brain acetylcholine and histamine in perphenazine catatonia and influence of antidepressants and diphenhydramine alone and in combination. Neuropharmacology 1975;14:555-60.  Back to cited text no. 19      
20.Uvans B. Mast cells and histamine release. Ind J Pharmacol 1969;1:23-32.  Back to cited text no. 20      



 
 
    Tables

  [Table 1], [Table 2]



 

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