Abstract

The bark of Mimosa tenuiflora (Willd.) Poiret (Leguminosae family), popularly known as “jurema preta” in Brazil, is used by the population of Contendas of Sincorá (Bahia State, Brazil) for the treatment of coughs and wound healing. Thus, the aim of this study was to evaluate the antinociceptive and anti-inflammatory activities of the bark ethanol extract (EEMT) and solvent soluble fractions (hexane—H, DCM—D, EtOAc—E and BuOH—B) of the extract in vivo. Additionally, we synthesized 5,7-dihidroxy-4’-methoxyflavanone (isosakuranetin) and isolated the compound sakuranetin, and both compounds were also tested. The anti-inflammatory and antinociceptive assays performed were: writhing test; nociception induced by intraplantar formalin injection; leukocyte recruitment to the peritoneal cavity; evaluation of vascular permeability (Evans blue test); and evaluation of mechanical hypernociception (von Frey test). Production of TNF-α, IL-10, myeloperoxidase and the expression of ICAM-1 were also evaluated. Statistical analysis was performed by one-way ANOVA followed by the Bonferroni post-test (n = 8), with P < 0.05. The EEMT showed antinociceptive activities in writhing test (100–200 mg/kg), in the second phase of the formalin test (50–200 mg/kg), and in mechanical hypernociception (100 mg/kg). EEMT showed an anti-inflammatory effect by reducing neutrophil migration to the peritoneal cavity and in the plantar tissue detected by the reduction of myeloperoxidase activity (100 mg/kg), reduction of IL-10 levels and expression of ICAM-1 in the peritoneal exudate and the mesentery (100 mg/kg), respectively. The four soluble EEMT fractions showed good results in tests for antinociceptive (H, D, E, B) and anti-inflammation (H, D, E). Only sakuranetin showed reduction of the writhing and neutrophil migration (200 mg/kg). Thus, the EEMT and soluble fractions of M. tenuiflora bark demonstrated great antinociceptive and anti-inflammatory activities, as also sakuranetin. More studies should be conducted to elucidate the mechanism of action of this compound. To the best of our knowledge, this is the first report on the antinociceptive activity of the M. tenuiflora fractions and the bioactive isolated compound sakuranetin in vivo.

Highlights

  • Inflammation is characterized by pain, redness, swelling and dysfunction of the tissues and organs and is the normal result of host protective responses to tissue injury caused by numerous stimuli [1,2]

  • In previous studies dealing with this plant, isosakuranetin (5,4’-dihydroxy-7-methoxyflavanone) was identified as the main flavone present in the extract; the literature NMR data for these two isomers are confusing

  • Indomethacin was purchased from Merck Sharp & Dohme (São Paulo, SP, Brazil), Tumor necrosis factor- α (TNF-α) and interleukin-1β (IL-1β) were purchased from R&D Systems (Pittsburgh, PA, USA)

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Summary

Introduction

Inflammation is characterized by pain, redness, swelling and dysfunction of the tissues and organs and is the normal result of host protective responses to tissue injury caused by numerous stimuli (e.g., physical trauma, chemicals and infectious agents) [1,2]. Inflammation is a hallmark of many chronic diseases; the long-term use of steroids and/or non-steroid anti-inflammatory drugs leads to hormonal side effects and gastric lesions in many instances [3,4]. Inflammation is commonly associated with pain as a secondary process due to the secretion of algesic mediators [5]. Pain represents the primary symptom for the diagnosis of several disease conditions and is widely accepted as one of the most important determinants of quality of life. Most conventional pain therapies are unsatisfactory in terms of efficacy, tolerability and toxicity [6]. Despite recent progress in the development of therapy, there is still a need for effective and potent analgesics and anti-inflammatories, especially for the treatment of chronic pain

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