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.
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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.
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