Alkylamides from Acmella oleracea: antinociceptive effect and molecular docking with cannabinoid and TRPV1 receptors

被引:9
|
作者
Kao Yien, Raissa M. [1 ]
Gomes, Anne Caroline C. [2 ]
Fiorot, Rodolfo Goetze [3 ]
Palhares Miranda, Ana Luisa [1 ]
Neves, Gilda A. [4 ]
Andrade, Brenda da Silva [4 ]
Costa, Fernanda N. [5 ]
Mendonca Tributino, Jorge Luiz [4 ]
Simas, Naomi Kato [1 ]
机构
[1] Univ Fed Rio de Janeiro, Fac Farm, Programa Posgrad Ciencias Farmaceut, Rio De Janeiro, Brazil
[2] Inst Fed Educ Ciencia & Tecnol Rio de Janeiro, Campus Realengo, Rio De Janeiro, Brazil
[3] Univ Fed Fluminense, Inst Quim, Dept Quim Organ, Niteroi, RJ, Brazil
[4] Univ Fed Rio de Janeiro, Inst Ciencias Biomed, Rio De Janeiro, Brazil
[5] Univ Fed Rio de Janeiro, Inst Pesquisa Prod Nat Walter Mors IPPN, Rio De Janeiro, Brazil
关键词
jambu; spilanthol; alkamides; cannabimimetics; R; K; JANSEN; FLOWERS; ISOBUTYLAMIDES; ACTIVATION; CAPSAICIN; ECHINACEA; LIGANDS; EXTRACT; MICE; CB2;
D O I
10.1080/14786419.2022.2142221
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Alkylamides are secondary metabolites in Acmella oleracea and display wide applications in treating several diseases. Since alkylamides can inhibit pain, this work aims to evaluate the antinociceptive profile of A. Oleracea methanolic extracts used in vivo and in silico assays. The extracts inhibited the neurogenic and inflammatory phases of the formalin test, ratifying the antinociceptive effect of alkylamides. Furthermore, the results from molecular docking demonstrated the interaction of A. oleracea alkylamides with the CB1/CB2 and TRPV1 receptors. Additionally, the crude methanolic extract of flowers did not induce potential side effects related to the classical cannabinoid tetrad: hypolocomotion and catalepsy. In conclusion, this work confirms the potential of the alkylamides of A. Oleracea as antinociceptive agents and, for the first time, correlates its effects with the endocannabinoid and vanilloid systems through in silico assays.
引用
收藏
页码:3136 / 3144
页数:9
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