Antinociceptive activity of ethanolic extract of Azadirachta indica A. Juss (Neem, Meliaceae) fruit through opioid, glutamatergic and acid-sensitive ion pathways in adult zebrafish (Danio rerio).

Biomed Pharmacother

Laboratory of Natural Product Bioprospecting and Biotechnology (LBPNB), Universidade Estadual do Ceará, Department of Chemistry, Campus CECITEC, Tauá, Ceará, Brazil; Laboratory of Biotechnology and Molecular Biology (LBBM), Universidade Estadual do Ceará, Centro de Ciências da Saúde, Campus Itaperi, Fortaleza, Ceará, Brazil; Laboratory of Natural Product Chemistry (LQPN-Block S), Universidade Estadual do Ceará, Centro de Ciências e Tecnologia, Campus Itaperi, Fortaleza, Ceará, Brazil; Experimental Biology Nucleus (NUBEX), Universidade de Fortaleza, Fortaleza, Ceará, Brazil. Electronic address:

Published: December 2018

Neem fruit (Azadirachta indica A. Juss.) are popularly used to treat infections, diarrhea, fever, bronchitis, skin diseases, infected burns and hypertension. Although the antinociceptive and anti-inflammatory potential of A. indica has already been investigated in experimental models of pain and inflammation in mice, the current research is the first to report the evaluation of the capacity of A. indica fruit ethanolic extract (EtFrNeem) in acute pain attenuation using the adult zebrafish (Danio rerio) as an alternative model to the use in rodents. EtFrNeem was submitted to antioxidant action, preliminary chemical prospecting, FT-IR and determination of phenol and flavonoid content tests. Subsequently, EtFrNeem was tested for acute nociception and abdominal inflammation, locomotor activity, and acute toxicity in adult zebrafish. Possible neuromodulation mechanisms were also evaluated. EtFrNeem showed low antioxidant activity, but was shown to be rich in flavonoids. EtFrNeem showed no anti-inflammatory action, did not alter the locomotor system, and it was not toxic. However, EtFrNeem significantly reduced the nociceptive behavior induced by formalin, glutamate and acidic saline, when compared to the control group. These effects of EtFrNeem were significantly similar to those of morphine, used as a positive control. The antinociceptive effect of EtFrNeem was inhibited by naloxone, ketamine and amiloride. EtFrNeem has the pharmacological potential for acute pain treatment and this effect is modulated by the opioid system, NMDA receptors and ASICs channels. These results lead us to studies of isolation and characterization of EtFrNeem bioactive principles, using adult zebrafish as an experimental model.

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Source
http://dx.doi.org/10.1016/j.biopha.2018.08.160DOI Listing

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