Abstract

The aim of the current study is to evaluate the anti-inflammatory, antioxidant and analgesic properties of ethanolic (100 and 200 mg/kg, p.o.) and ethyl acetate extracts (100 and 200 mg/kg, p.o.) of Caralluma europaea. Formalin-induced paw licking test, Acetic Acid induced Writhing Test and Hot-PlateTest were used to assess the analgesic activity. Xylene-induced ear edema test was used to evaluate anti-inflammatory activity of those extracts. In this work, the High-Performance Liquid Chromatography technique (HPLC), allowed us to identify and quantify the main phenolic compounds present in ethanolic and ethyl acetate extracts. In vitro anti-oxidant propriety was evaluated using two methods, the 2,2-Diphenyl-1Picrylhydrazyl (DPPH) radical scavenging method and reducing power methods. The main phenols identified were Catechin (24%) and quercetin (18%) in ethanolic extract, while in the ethyl acetate extract, they were quercetin (36%), P-coumaric (30%) and 2-hydroxycinnamic (25%). Analysis of our results had shown that Caralluma europaea extracts had exhibited a very potent analgesic activity. Percentage of Pain Inhibition (PPI) in the writhing test, 63.60±4.24% for the Ethanolic Extract (EE) (200 mg/kg, p.o.) and 65.39±3.27% for the Ethyl Acetate Extract (EAE). The PPI of early and late phase in the formalin test were respectively, 41% and 73% for EAE (200 mg/kg; p.o), 28% and 75% for EE. In the hotplate test, latency to the thermal stimuli was increased in a dose dependent manner after the administration of EE and EAE. However, the analgesic potential of EAE seems to be higher than EE. Both EE and EAE presented a significant in vitro redox potential and high anti-inflammatory activity. Our results have shown that Caralluma europaea is rich in phenolic compounds and possesses an important antinociceptive, anti-inflammatory and anti-oxidant activity.

Highlights

  • Inflammation and pain are main preservative responses protecting the organisms counter physical, chemical and pathological alterations (Ezeja et al, 2011)

  • In this study the evaluation of in vivo test on mice for the acute toxicity of the two extract of C. europaea showed that the (LD50) is greater than 5 g/kg, no mortality or signs of toxicity and no change body weight wasn't observed during the 48 h following single dose administration (0.5, 1, 2.5 and 5 g/kg body weight) of each of the two Caralluma europaea extracts

  • These results suggest that Ethanolic Extract (EE) and Ethyl Acetate Extract (EAE) have analgesic action at the central and peripheral levels

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Summary

Introduction

Inflammation and pain are main preservative responses protecting the organisms counter physical, chemical and pathological alterations (Ezeja et al, 2011). The inflammatory response is produced by blood flow changes and escape of cells from the blood into the tissues due to the increased blood vessels permeability (Habashy et al, 2005). Control of pain and inflammation is one of the main therapeutic goals (Ezeja et al, 2011). Due to the limited application and adverse effects of synthetic drugs, plant and natural product extracts are being explored for their therapeutic properties

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