The Effect of Saliva Officinalis Hydroalcoholic Extract on Analgesic Effect of Morphine in Rat

Document Type : Original Article

Authors

1 Department of Pharmacology. Toxicology, School of Pharmacy Physiology Research Center

2 Physiology Research Center & Medicinal Plant Research Center.

3 Department of Pharmacocnosy. School of Pharmacy.

4 Department of Toxicology School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

Abstract

Background and Objective: There are some reports in Iranian traditional medicine concerning the anti-inflammatory effect of Saliva Officinalis (SO). In the present study with the aim of decreasing analgesic dose of morphine, analgesic effect of different doses of SO hydroalcoholic extract alone and associated with morphine were evaluated by tail flick in rats.
Subjects and Methods:  Analgesic effects of SO hydroalcholic extract at doses of 200, 400, 600, 800 and 1000 mg/kg, i.p. were investigated. Then the influence of these doses associated with analgesic dose of morphine (2.5 mg/kg) was evaluated. Rats were placed into restrainer and then transferred into the tail flick apparatus with the intensity 55 Cº and cut off time= 10 sec. In order to verify the role of opioid receptors on analgesic effect of SO extract, naloxone (1mg/kg, i.p.) was administered to one group of rats 15 min before receiving 800 mg/kg extract. Then, the data were analyzed by two-way ANOVA followed by LSD post hoc test and significant difference between groups was accepted with P<0.05.
Results: The Data have shown that, the SO extract relieved pain in tail-flick test dose dependently and the most effective dose was 800 mg/kg. The maximum analgesic effect of the extract combined with morphine was observed at time point 45 min. Naloxane, opioid receptor antagonist could reduce analgesic effect of the extract.
Conclusion: On the basis the results obtained in this study, it could be suggested that the SO extract potentiates morphine anti-nociceptive effect and this means that the opioid system may be involved in the analgesic effect of this plant extract.
Sci Med J 2011;10(5):505-13

Keywords


 
1-Chauchar  P. Recognition and pain remedy. 4th ed . afsharnadari Q, translator. Tehran: Gostardeh Nashr Publications; 1990: p. 13-14.
2-Kandel Eric R, Schwarts JH. Principles of neural science. 4th ed. USA: elsevier; 2000: Chap 24, P.472-89.
3-Mozaffarian V. A dictionary of Iranian plant names. Tehran: Farhany moaser; 2007: P. 617.
4-Carol A, Linda A, Anderson J, Philipson D. Herbal medicines. 1996; 231-32.
5-Zargari A. Medicinal plants. 4th ed. Tehran: Tehran University Press; 1990: P. 62.
6-Samsam Shariat H. Qualitative and quantitative evaluation of the action constituents and control methods for medicinal plants. 1st ed. Isfehan: Mani publications; 1992: P. 12-20.
7-Beladi Nejad M. The stady of the effect of hydro alcoholic extract of Artemisia dracunculus L. on analgesic effect of morphine in rat  [dissertation]. Ahvaz: Ahvaz  jundishapour University of Medical Sciences; 2006: P. 65-6.
8-Volak JS, Todola J. Plants medicinalis. 3rd ed. Zaman S, translator. Tehran: Ghoghnus; 1997: P. 296.
9-Lynch  MA. Long- term potentiation and Memory. Physiol Rev. 2004; 84(1): 87-136. [PMID: 14715912]
10-Kavvadias D, Sand P, Youdim KA, Qaiser MZ, Rice-Evans C, Baur R, et al. The flavone hispidulin, a benzodiazepine receptor ligand with positive allosteric properties, traverses the blood-brain barrier and exhibits anticonvulsive effects. Br j Pharmacol. 2004; 142(5): 811-20. [PMID: 15231642]
11-Pereira P, Tysca D, Oliveira P, Dasilbabrum IF, Picada JN, Ardenghi P. Neurobehavioral and genotoxic aspects of rosemarinic acid. Pharmacol Res. 2005; 52(3): 199-203. [PMID: 16026713]
12-Abu-Amer KM, Sen P. Pharmacology of rosemary and its therapeutic potentials. Indian J Exp Biol. 1999; 37(2): 124-30. [PMID: 10641130]