Orofacial antinociceptive effect of Mimosa tenuiflora (Willd.) Poiret

Mimosa tenuiflora (Willd.) Poiret, popularly known in Brazil as “jurema-preta” is widely used against bronchitis, fever, headache and inflammation. Its antioxidant, anti-inflammatory and antinociceptive potential has already been reported. To assess the orofacial antinociceptive effect of M. tenuifl...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2018-01, Vol.97, p.1575-1585
Hauptverfasser: Magalhães, Francisco Ernani A., Batista, Francisco Lucas A., Serpa, Ohanna F., Moura, Luiz F. Wemmenson G., Lima, Maria da Conceição L., da Silva, Ana Raquel A., Guedes, Maria Izabel F., Santos, Sacha Aubrey A.R., de Oliveira, Breytiner A., Nogueira, Andressa B., Barbosa, Talita M., Holanda, Dayse Karine R., Damasceno, Marina B.M.V., de Melo, José de Maria A., Barroso, Lana Karine V., Campos, Adriana R.
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Sprache:eng
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Zusammenfassung:Mimosa tenuiflora (Willd.) Poiret, popularly known in Brazil as “jurema-preta” is widely used against bronchitis, fever, headache and inflammation. Its antioxidant, anti-inflammatory and antinociceptive potential has already been reported. To assess the orofacial antinociceptive effect of M. tenuiflora, ethanolic extracts of M. tenuiflora (leaves, twigs, barks and roots) were submitted to in vitro tests of antioxidant activity. The extract with the highest antioxidant potential was partitioned and subjected to preliminary chemical prospecting, GC–MS, measurement of phenolic content and cytotoxicity tests of the fraction with the highest antioxidant activity. The nontoxic fraction with the highest antioxidant activity (FATEM) was subjected to tests of acute and chronic orofacial nociception and locomotor activity. The possible mechanisms of neuromodulation were also assessed. The EtOAc fraction, obtained from the ethanolic extract of M. tenuiflora barks, was the one with the highest antioxidant potential and nontoxic (FATEM), and Benzyloxyamine was the major constituent (34.27%). FATEM did not alter the locomotor system of mice and reduced significantly the orofacial nociceptive behavior induced by formalin, glutamate, capsaicin, cinnamaldehyde or acidic saline compared to the control group. FATEM also inhibited formalin- or mustard oil-induced temporomandibular nociception. In addition, it also reduced mustard oil-induced orofacial muscle nociception. However, FATEM did not alter hypertonic saline-induced corneal nociception. Neuropathic nociception was reversed by treatment with FATEM. The antinociceptive effect of FATEM was inhibited by naloxone, L-NAME and glibenclamide. FATEM has pharmacological potential for the treatment of acute and neuropathic orofacial pain and this effect is modulated by the opioid system, nitric oxide and ATP-sensitive potassium channels. These results lead us to studies of isolation and characterization of bioactive principles.
ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2017.11.001