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Original Research Article | OPEN ACCESS

In vivo analgesic activities and safety assessment of Vitis vinifera L and Punica granatum L fruits extracts

Zeghad Nadia1,2 , Madi Aicha1, Helmi Sihem1, Belkhiri Abdelmalik1,3

1Laboratoirede pharmacologie et de toxicologie; 2Faculté des Sciences de la Nature et de la Vie; 3Laboratoire de pharmacognosie, Faculté de médecine, Université des frères Mentouri Constantine 3, Algérie.

For correspondence:-  Zeghad Nadia   Email: zeghadnadia@umc.edu.dz

Received: 15 August 2015        Accepted: 22 February 2016        Published: 31 March 2017

Citation: Nadia Z, Aicha M, Sihem H, Abdelmalik B. In vivo analgesic activities and safety assessment of Vitis vinifera L and Punica granatum L fruits extracts. Trop J Pharm Res 2017; 16(3):553-561 doi: 10.4314/tjpr.v16i3.8

© 2017 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the analgesic properties of hydro-alcohol fruit extracts of Vitis vinifera (grape) and Punica granatum (pomegranate) in albino male mice.
Methods: The analgesic activity of the fruit extracts was examined in vivo using thermal stimulus assays (tail immersion and hot plate) and chemically-induced writhing test. The extracts were administered orally at doses of 1.0, 2.0 and 3.0 g/kg. Acetylsalicylic acid (0.1 g/kg, per os) was used as analgesic drug. 
Results: In acetic acid writhe test, pre-treatment with both extracts significantly decreased (p < 0.0001) in a dose-dependent manner the number of writhes when compared to control. Vitis vinifera extract treatment caused pain inhibition index values of 36.52 % (1.0 g/kg), 66.67 % (2.0 g/kg) and 89.71 % (3.0 g/kg). Corresponding values for Punica granatum extract treatment were 45.39 % (1.0 g/kg), 70.93 % (2.0 g/kg) and 86.88 % (3.0 g/kg). Acetylsalicylic acid treatment produced 76.06 % of pain inhibition. There were no significant differences (p < 0.05), at equivalent doses of 2.0 and 3.0 g/kg between Vitis vinifera and Punica granatum extract treatments regarding reduction in number of writhes. In hot-plate test, both extracts increased reaction latency time. In tail-immersion assay, Punica granatum significantly increased response to heat stimulus at doses of 2.0 g/kg (p < 0.05) and 3.0g/kg (p < 0.001) compared to control.  However, Vitis vinifera did not produce such effects at any of the doses used.
Conclusion: These results show that the hydro-alcohol fruit extract of Punica granatum has a superior analgesic effect to that of Vitis vinifera extract.

Keywords: Vitis vinifera, Pomegranate, Punica granatum, Thermal stimulus assay, Analgesic activity, Pain

Introduction

Drugs presently used for management of pain and inflammatory conditions are either NSAIDs or opiates [1]. Most of these medicines have risk of adverse side effects (like gastric lesions caused by NSAIDs and tolerance and dependence induced by opiates); and their analgesic effects are not effective in all cases [2]. According to World Health Organization, traditional herbal remedies are still extensively used, especially in rural regions with restricted access to modern medicines [3]. Investigation of pain relief potential of plant-based remedies used in traditional medicine is one viable way of discovering new analgesic agents which could be beneficial in pain management [4].

An ethno-pharmacological survey of plant-based remedies commonly used to relieve pain, conducted as part of our research program on traditional medicinal plants of the Maghreb region has resulted in establishment of a priority list of plants, among are two well-known species, Vitis vinifera (grape) and Punica granatum, (pomegranate). These plants are extensively cultivated in Tunisia and Morocco for their socio-economic values. Both species produce juicy and sweet fruits. Their therapeutic uses in traditional medicine are well documented in the literature of North Africa traditional medicine through several comprehensive reviews [5-8].

Vitis vinifera L. (Vitaceae), known locally as "Dalya", is a climbing shrub native to the Mediterranean region, Central Europe and South-Western Asia [9]. The leaves, fruits and seeds of this plant possess astringent, homeostatic and anti-inflammatory properties [9,10]. Parts of the plant are traditionally utilized to stop bleeding, inflammation, and also remedy for painful conditions due to hemorrhoids and headaches [7]. Studies have shown that the leaves and fruits of Vitis vinifera are rich in flavonoids (kampferol-3-0-glucosides, quercetin-3-O-glucosides); tannins (procyanidolic oligomers); stilbenes (resveratrol and viniferins); phenolic acids (tartaric acid, malic acid, succinic acid, citric acid and oxalic acid); and phenylacrylic acid derivatives (p-coumaroyl acid, caffeoyl acid and feruloylsuccinic acid) [11,12]. From a pharmacological point of view, in vitro and in vivo studies have reported a wide range of biological effects, including anti-inflammatory, anti-oedematous, hepatoprotective, antimicrobial, antioxidative, vasorelaxant and spasmolytic effects [13].

Punica granatum L. (Lythraceae), locally called "Rouman", is a fruit-bearing shrub native to the Middle East but now widely cultivated in warm regions of the world, particularly throughout the Mediterranean region [14-16]. Pomegranate is a used for the nutritional and medicinal benefits of its fruits [16,17]. The entire fruit is used in folklore medicine as remedy for various diseases such as dyspepsia, ulcer, hepatic damage, jaundice and diarrhea, as well as relief of pain from sore throat and menstruation [7,18]. The chemistry and pharmacology of Punica granatum has been recently reviewed [19]. The fruit contains polyphenols such as ellagic acid, punicic acid, ellagitannin, punicalagin, anthocyanidins, oestrogenic flavonols and flavones [19,20]. Pharmacological studies have established its antimicrobial, antioxidant, anti-inflammatory, anti-helminthic and molluscicidal properties [18,19]. Other benefits of pomegranate include chemopreventive potential of pomegranate ellagitannin against prostate cancer [21].

The current study was carried out to investigate the possible protective roles of hydro-alcohol fruits extracts of Vitis vinifera and Punica granatum against pain induced in mice by chemical and thermal methods.

Methods

Plant materials

Plant materials were purchased from local market from the 2012 harvest season. Samples of black grape (Vitis vinifera L.) and pomegranate (Punica granatum L), were authenticated by a taxonomist.

Mature fresh fruits of the two species were collected in bulk, and washed under running tap water to remove dirt and adhering materials. The edible portion of the fruits was freeze-dried, powdered using a dry grinder and stored at low temperature (-25 ºC) until extracted.

Drugs and chemicals used

Acetic acid, acetylsalicylic acid and other chemicals used for extraction purpose and phytochemical screening were purchased from Sigma Aldrich.

Extraction process

The extraction process was carried out according to the methods of Babero et al and Ma et al [22,23]. Samples (25 g) were extracted by maceration for 24 h with 500 ml of methanol: water (70:30 v:v) in an automatic shaker. The extraction was assisted by ultrasound for 30 minutes at room temperature, and the debris was re-extracted twice under identical conditions.

The extracts from each plant were combined and filtered, and the combined filtrate was concentrated in a rotary evaporator under vacuum at low temperature (< 40 °C) to yield the crude extract which was subjected immediately to lyophilization. Freeze dried samples were kept at low temperature (-25 °C) until required for further experiments. Extracts of both species were reconstituted in distilled water for the evaluation of analgesic activity.

Phytochemical screening

Phytochemical analysis of crude extracts of both species was done using standard reactions of biological active groups i.e. flavonoids, tannins, alkaloids, saponins, steroids, terpenoids, and coumarins [24,25].

Experimental animals

Adult albino mal mice, weighing between 20-32 g and aged (4-5) weeks were used for the studies. The animals were kept in standard polypropylene cages at room temperature (24 ± 2°C) in a 12 h light/dark cycle. They were allowed access to standard pellet diet and water ad libitum, and were acclimatized to the laboratory conditions for seven days before the experiment. The study was carried out following the guidelines prescribed in Guide for the Care and Use of Laboratory Animals [26].

Acute toxicity study

After an overnight fast, healthy animals were weighed and randomly distributed into 5 groups of six animals each (one control group and four treated groups). The animals were fed by oral gavages using a specially designed mice needle. The control and extract-treated groups received per os distilled water and serial doses (0.5, 2.5, 5.0 and 10.0g/kg) of extracts reconstituted in distilled water, respectively. Animals observation was carried within the first 30 minutes, then periodically during the first 24 hours and once daily for two weeks. Death or changes in general behavior and other physical activities were noted [27,28].Mice of all groups were weighted on days 7th and 14th. At the end of the experiment, the animals were scarificed and their internal organs including heart, liver, kidneys, lungs, spleen were examined [29,30].

Determination of analgesic activity

Analgesic activity was measured by three different methods: chemically-induced writhing, hot-plate and tail-immersion assays, as previously reported [31]. The peripheral analgesic effect of the extracts was evaluated by chemically- induced writhing test [32-34], while the involvement of central mechanisms was studied by using the hot-plate and tail-immersion tests. The latter assays are known to activate supra-spinal and spinal nociceptive pathways, respectively [35]. Tests were conducted after 24 h fast; healthy animals were then weighed and randomly distributed into groups of six animals each (n = 6).

Acetic acid-induced writhing test

The method described initially by Collier et al [36], was used. Writhing was elicited by an intraperitoneal (i.p) injection of 1 % acetic acid solution. Animals (6 per groups) were pretreated with fruits extracts of Vitis vinifera or Punica granatum (1.0, 2.0 and 3.0 g/kg, per os, single dose) reconstituted in distilled water, or acetylsalicylic acid (standard drug, 0.1 g/kg, per os). Then they were allowed to adapt for 60 min before intraperitoneal (i.p.) injection of acetic acid solution. The number of writhes in 20 min was counted for each mouse. Pain inhibition index [PII] was expressed as in Eq 1.

PII = [(Nc-Nt)/Nc] × 100 ……………………. (1)

where Nc represents the number of writhes observed for control group, and Nt the number of writhes in test groups (fruits extracts, acetylsalicylic acid).

Evaluation of central analgesic activity

Central analgesic activity was monitored using two standard mechanical methods, the hot plate and tail immersion tests.

Hot plate test

Hot plate test was performed according to the method described earlier [33]. Five groups of mice (6 mice per group) were used. They received, one hour before test, fruit extracts of Vitis vinifera or Punica granatum at different concentrations (1.0, 2.0 and 3.0 g/kg, single dose, per os), distilled water (control), or acetylsalicylic acid as anti-inflammatory drug (0.1 g/kg, per os). The animals were placed on a heated surface of a hot plate maintained at 55.0 ± 0.5 °C. Pain threshold was considered reached when the animals licked their hind paws or jumped out [37].

Tail immersion test

Tail immersion test was performed according to the method described before [34]. Five groups of mice (6 mice per group) were used. They received, one hour before testing, fruits extracts of Vitis vinifera or Punica granatum at different doses (1.0, 2.0 and 3.0 g/kg, single dose, per os), distilled water (control), or acetylsalicylic acid as anti-inflammatory drug (0.1 g/kg, per os). The lower portion of the animal tail was immersed gently in a hot water bath maintained at 55.0 ± 0.5 °C. The reaction time taken by the animal to withdraw its tail was recorded (using a chronometer), after administration of treatments [38].

Statistical analysis

The results of pharmacological testing were expressed as mean ±SD and analyzed by Tukey test (HSD) to determine the level of significance. A value of P<0.05 was considered to be significantly. Statistical analyses were performed using XL Stat version.

Conclusion

The findings of this study demonstrate that the hydro-alcohol fruit extracts of Vitis vinifera and Punic agranatum exhibit significant analgesic activities in mice. These findings confirm results of previously reported studies on analgesic activity of Vitis vinifera and Punica granatum, and indicate that these two plants may offer alternative herbal treatments for the management of pain and inflammatory conditions.

Declarations

Acknowledgement

Authors are thankful to the laboratory of Botany and Pharmacognosy, Medical Faculty, Constantine University 3, for their help in identification and authentication of the plants.

References

  1. Rang HP, Urban L. New molecules in analgesia. Brit J Anaesth. 1995;75 : 145-156.
  2. Sostres C, Gargallo CJ, Lanas A. Nonsteroidal anti-inflammatory drugs and upper lower gastrointestinal mucosal damage. Arthrit Res & Therapie. 2013; 15(3): 1-8.
  3. Ammara H, Rahman S, Deeba F, Shahid M. Antimicrobial activity of some plant extracts having hepatoprotective effects. J. Med. Plants Res. 2009;3(1): 20-23.
  4. Salim AA. Chin Y W, Kinghorn AD. Drug Discovery from Plants (in Bioactive Molecules and Medicinal Plants. Ramawat K.G. Mérillon J-M. (Eds). Berlin: Springer-Verlag, Heidelbe.2008; pp 1-18.
  5. Boulos L. Medicinal plants of North Africa. References Publications, Inc Michigan.1983.
  6. Muhammad Ibn Hamadush A.  Révélation des énigmes dans l’exposition des drogues et des plantes, (Traduction de Leclerc L.). Beirut:  Dar al-Kotob al-Ilmiya.1996.
  7. Baba Aissa F.  Encyclopédie des plantes utiles.Edition El-Maarifa. 2011.
  8. Bellakhdar J. La pharmacopée marocaine traditionnelle, médecine arabe ancienne et savoirs populaires. Paris:IbisPressEditions. 1997; 320-321.
  9. Min H. Henglu T. Xiaowen L. Xiaohua Q. Xuehao C. Molecular progress in research on fruit astringency. Molecules.2015; 20: 143-151.
  10. El Hawary S, El Fouly  K, El Gohary  HM, Meselhy KM, Salem A, Talaat Z. Phytochemical and biological investigation of Vitis vinifera L. (Flame cultivars), Vitaceae cultivated in Egypt. Nat sci. 2012; 10(10): 48-59.
  11. Ruaa AJ, Denisa M, Dogaru E. Study regarding the influence of Vitis vinifera fruit (Muscat of Hamburg species) on some biochemical parameters. Farmacia.2010; 58(3): 332-340.
  12. Monica M. Vitis vinifera (Grape) ingredients as used in cosmetics, Scientific Literature Review. 2012; 1-29p.
  13. European Medicines Agency. Assessment report on Vitis vinifera L., folium. Committee on herbal medicinal products (HMPC).[cited2010]. Available from : (www.ema.europa.eu)
  14. Saad H, Charrier El Bouhtoury F, Pizzi A, Rode K, Charrier B, Ayed N. Characterization of pomegranate peels tannins extractives. Ind crop prod. 2012; 40: 239-246.
  15. Raafat K, Samy W.  Amelioration of diabetes and painful diabetic neuropathy by Punica granatumL extract and its spray dried biopolymeric dispersions, Hindawi publishing corporation; Evidence-based complementary and alternative medicine. 2014; 1-12p.
  16. Debjit B, Harish G, Pragati Kumar B, Duraivel S, Aravind G, Sampath Kumar KP. Medicinal uses of Punica granatum and its health benefits. J Pharmacogn&Phytochem.2013; 1(5): 28-35.
  17. Bellakhdar J. Le Maghreb à travers ses plantes. Barzakh Editions. 2013; 138-141p.
  18. RaneZab AK, Anusha B. Phytochemical evaluation by GC-MS and in vitro antioxidant activity of Punica granatum fruit rind extract. J Chem& Pharm res. 2012; 4(6): 2869-2873.
  19. Garach D, Pake A, Chakraborty M, Kamath JV. Phyochemical and pharmacological profile of Punica granatum: an overview.  Intr Res J Pharm.2013; 3(2): 65-68.
  20. Farag R, Abdelatif M, Emam S, Tawfeek L. Phytochemical screening and polyphenol constituents of pomegranate peels and leave juices. Agr& soil sci.2014; 1(6): 86-93.
  21. Heber D. Multitargeted therapy of cancer by ellagitannins. Cancer Lett.2008; 269: 262–268.
  22. Babero GF, Liazid A, Palma M, Barroso CG. Ultrasound assisted extraction of capsaicinoids from peppers. Talanta. 2008; 75(5): 1332-1337.
  23. Ma YQ, Chen JC, Liu DH, Ye XQ. Simultaneous extraction of phenolic compounds of Citrus peel extracts: effect of ultrasounds. Ultrasonsonochem.2009 ;16 (1): 57-62.
  24. Kokate KC. Practical pharmacognosy, 4th edition, Delhi: VallabhPrakashan. 1997;128p.
  25. Harborne JB. Phytochemical methods: a guide to modern techniques of plant analysis, 2nd edition, London: Chapmand and Hall. 1998; 54-84p.
  26. Guide for care and use of laboratory animals. National Academy of Sciences Committee for the Update of the Guide for the Care and Use of Laboratory Animals, the National Academies Press, 8e edition.2011.
  27. Shah Ayub MA, Garg SK, Garg KM. Subacute toxicity studies on Pendimethalin in rats. Indian J Pharmacol.1997; 29: 322-324.
  28. Bürger C, Fischer DR, Cordenunzzi DA, Batschauer de Borba AP, Filho VC, Soares dos Santos AR. Acute and subacute toxicity of the hydroalcoholic extract from Wedeliapaludosa (Acmelabrasilinsis) (Asteraceae) in mice. JPharmacol Sci.2005 ;  8(2): 370-373.
  29. Thanabhorn S, Jaijoy K, Thamaree S, Ingkaninan K. Acute and subacute toxicities of the ethanol extract from the fruits of Terminaliabelerica (Gaertn) Roxb. J Pharm Sci. 2006; 33(1-4): 23-30.
  30. Pello C. Acute oral toxicity in rats «acute toxic class method» test item. Rapport confidential, CIT, Evreux.2005.
  31. Uma Shankar S, Umesh Kumar S, Abhishek S, Niranjan S, Puspak JS. Screening of Terminaliabellirica fruits extracts for its analgesic and antipyretic activities. Jordan J Biol Sci. 2010; 3(3):121-124.
  32. Koster R, Anderson M, Rehan HMS. Acetic acid analgesic screening. Federation proceeding. 1959; 18: 418.
  33. Taber RI, Greenhouse DD, Rendel JK, Irwin S. Agonist and antagonist interaction of opoids on acetic acid induced abdominal stretching in mice. JPharmacol.1969; 169: 29-37.
  34. Singh S, Maumder DK, Rehan HMS. Evaluation of anti-inflammatory potential of fixed oil of Ocimum sanctum (Holybasil) and its possible mechanism of action. J Pharm Pharmacol.1996; 38: 627.
  35. Wani TA, Kumar D, Prasad R, KumarVerma P, Sardar KK. Tandan SK. Kumar, D. Analgesic activity of the ethanolic extract of Shorearobusta resin in experimental animals. Indian J Pharmacol. 2012; 44(4):493-499.
  36. Collier HO, Dinneen LC, Johnson CA, Schneider C. The abdominal constriction response and its suppression by analgesic drugs in the mouse. BrJ PharmacolChemother. 1968; 32: 295-310.
  37. Naveed M, Saeed M, NaeemuddinGilani S, UlHaq I, Khan H. Analgesic and anti-inflammatory profile of n-Hexane fraction of Viola betonicifolia. Trop J PharmaceutRes. 2012; 11(6): 963-969.
  38. Hoque N, RazibulHabibiMd, Zafar Imam M, Jamiuddin A, SohelRana Md. Analgesic and anti-inflammatory potential of methanolic extract of Glinusoppositifolius L. AustJBasic &appl sci. 2011; 5(8):729-733.
  39. Kennedy GL, Ferenz RL, Burgess BA. Estimation of acute oral toxicity in rats by determination of the approximate lethal dose rather than the LD50.J Appl&Toxicol.1986; 6: 148-148.
  40. Paulino N, Dankas AP, Bankova V, Longhi DT, Scremin A de Castro SL, Calixto JB. Bulgarian propolis induces analgesic and anti-inflammatory effects in mice and inhibits airway smooth muscle. J. Pharmacol Sci.2003; 93: 307-313.
  41. Bektas N, Arslan R. Antinociceptive effects of methanol extract of Capparisovate in mice. Pharm Biol. 2010; 48: 1185-1190.
  42. Bentley GA, Newton SH, Starr J. Studies on the antinociceptive action of a-agonist drugs and their interactions with opioid mechanisms. Br J Pharmacol.1983; 79: 125-134.
  43. Ribeiro RA, Vale MI, Thomazzi SM, Paschoalato AB, Poole S, Ferreira SH, Cunha FQ. Involvement of resident macrophages and mast cells in the writhing nociceptive response induced by zymosan and acetic acid in mice. Eur J Pharmacol. 2000; 387: 111-118.
  44. Kartik JS, Sachdev D. Evaluation of antinociceptive and anti-inflammatory effect of the hydroalcoholic extracts of leaves and fruit peel of Punica granatum in experimental animals. Asian J Pharm &ClinRes.2010; 7 (2) : 137-141.
  45. Miguel MG, Neves MA, Antunes D. Pomegranate (Punica granatum L); A medicinal plant with myriad biological properties. J MedPlantsRes.2010; 4(25): 2836-2847.
  46. Sadaiah B, Sunil Kumar KT, Kavitha CN, ManoharBabu S, Prabhakar Reddy V. Antinociceptive activity of methanolic extract of leaves of Vitis vinifera. Der Pharm Sinica.2011;2(2) : 190-197.
  47. GunoSindhu C. Analgesic activity of various extracts of Punica granatum (linn) flowers. Int J green pharm. 2008; 2(3): 145-146.
  48. Priyanka B, Mohd A, Vidhu A, Shahnaz S, Malay B. Evaluation of anti-inflammatory and analgesic activity of Punica granatum L. Int J drug dev& res. 2010; 2 (4).
  49. Gupta JK, Sharma SK, Misra V, Patel K. Evaluation of anti-nociceptive and anti-inflammatory activity of Punica granatum seed extract. Int Res J Pharm. 2011; 2(12): 235-237.
  50. Nain P, Aini M, Malik M. Evaluation of anti-inflammatory and analgesic activity of Punica granatum linn leaves. Int J Res in Ayurveda & Pharm. 2011; 2(3): 987-990.
  51. Swarnamoni D, Renuka SS, Shagufa A, Lalit K. Analgesic and anti-inflammatory activities of ethanolic extract of leaves of Punica granatum L on experimental animal models.Pharmacol.2011;3: 379-385.
  52. Olapour S, Najafzadeh H. Evaluation analgesic, anti-inflammatory and antiepileptic effect of hydro alcoholic peel extract of Punica granatum (pomegranate). Asian JMedSci. 2010; 2(6): 266-270.
  53. Bensaad L, KahHwi K, Alsereti M, Shahimi M. Evaluation of the analgesic effects of Libyan fresh pomegranate fruit of Punica granatum. PharmaNutr. 2013;2: 75-119.
  54. Saad LB, Hwi KK, Quah T. Evaluation of the antinociceptive effect of the ethanolic extract of Punica granatum. AfrJ Trad Comp& relative Med.2014; 11 (3):228-232.
  55. Lamees ABS, Kah HK. Phytochemical constituents and analgesic activity of ethyl acetate fraction of Punica granatum L (Punicaceae). Trop J Pharm Res. 2015;14(1): 87-93.
  56. Jyoti S, Ajay KS, Anand S. Analgesic and anti-inflammatory activity of methanolic extract of Vitis vinifera leaves. Pharmacol.2009; 3:496-504.
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