Plants (Oct 2022)

Mechanisms of Actions Involved in The Antinociceptive Effect of Estragole and its <i>β</i>-Cyclodextrin Inclusion Complex in Animal Models

  • Roger Henrique Sousa da Costa,
  • Anita Oliveira Brito Pereira Bezerra Martins,
  • Renata Torres Pessoa,
  • Saad Ali Alshehri,
  • Shadma Wahab,
  • Md Faruque Ahmad,
  • Muath Suliman,
  • Lucas Yure Santos da Silva,
  • Isabel Sousa Alcântara,
  • Andreza Guedes Barbosa Ramos,
  • Maria Rayane Correia de Oliveira,
  • Francisco Lucas Alves Batista,
  • Gyllyandeson de Araújo Delmondes,
  • Pablo Antonio Maia de Farias,
  • Janaína Esmeraldo Rocha,
  • Henrique Douglas Melo Coutinho,
  • António Raposo,
  • Conrado Carrascosa,
  • José Raduan Jaber,
  • Irwin Rose Alencar de Menezes

DOI
https://doi.org/10.3390/plants11212854
Journal volume & issue
Vol. 11, no. 21
p. 2854

Abstract

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(1) Background: estragole is a monoterpene found in the essential oils of several aromatic plants, which can be used for several pharmacological activities. The aim of this study was to evaluate the antinociceptive effect of estragole (Es) and its β-cyclodextrins inclusion complex (Es/β-CD). (2) Methods: the effects of Es and Es/β-CD on the central nervous system (CNS) were evaluated through open field and rota-rod assays, and the antinociceptive effect in formalin models, abdominal writhing induced by acetic acid, hot plate, tail flick test and plantar mechanical hyperalgesia. (3) Results: Es and Es/β-CD showed no alterations on the CNS evaluated parameters and the results suggested there was an antinociceptive action in the formalin, abdominal writhing, hot plate, tail flick tests and plantar mechanical hyperalgesia, proposing the involvement of the nitric oxide, glutamatergic signaling pathways, cyclic guanosine monophosphate and vanilloid pathways. (4) Conclusion: the results suggest that Es and Es/β-CD have a promising antinociceptive potential as a possible alternative for the pharmacological treatment of pain, also showing that the encapsulation of Es in β-cyclodextrins probably improves its pharmacological properties, since the complexation process involves much lower amounts of the compound, contributing to better bioavailability and a lower probability of adverse effect development.

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