α-Terpineol, a monoterpene alcohol, complexed with β-cyclodextrin exerts antihyperalgesic effect in animal model for fibromyalgia aided with docking study.

Abstract

The anti-hyperalgesic effect of the complex containing α-terpineol (αTPN) and β-cyclodextrin (βCD) was analyzed in a non-inflammatory chronic muscle pain model, as well as its mechanism of action through docking study for a possible interaction with receptors. The αTPN-βCD complex was prepared and characterized through the thermogravimetry/derivate thermogravimetry (TG/DTG), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). The model of chronic muscle pain was induced by two injections of pH 4.0 saline (20 μl) into the left gastrocnemius 5 days apart. After confirming hyperalgesia, male mice were treated with αTPN-βCD (25, 50 or 100 mg/kg; p.o.) or vehicle (saline 0.9%, p.o.) daily for 10 days. 1 h after the mechanical hyperalgesia, motor performance was evaluated. In addition, the systemic administration of naloxone and ondansetron tested the analgesic effect on the active opioid and serotonin receptors, respectively. The characterization tests indicated that αTPN was efficiently incorporated into βCD. The oral treatment with αTPN-βCD, at all doses tested, produced a significant (p < 0.001) decrease in the mechanical hyperalgesia, without causing any alteration in the force and in motor performance. This analgesic effect was reversed by the systemic administration of naloxone or ondansetron. These findings are corroborated by the docking study described in the present study, which verified a possible interaction of αTPN-βCD with opioid (MU, Kappa, Delta) and 5-HT receptors. Thus, it can be concluded that αTPN-βCD reduced the hyperalgesia followed by the chronic muscle pain model, probably evoked by the descending inhibitory pain system, specifically by opioid and serotoninergic receptors.

• Authors: Makson G B Oliveira, Renan G Brito, Priscila L Santos, Heitor G Araújo-Filho, Jullyana S S Quintans, Paula P Menezes, Mairim R Serafini, Yasmim M B G Carvalho, Juliane C Silva, Jackson R G S Almeida, Luciana Scotti, Marcus T Scotti, Saravanan Shanmugam, Parimelazhagan Thangaraj, Adriano A S Araújo, Lucindo J Quintans-Júnior
• Journal: Chemico-biological interactions (Chem Biol Interact) Vol. 254 Pg. 54-62 (Jul 25 2016) ISSN: 1872-7786 [Electronic] Ireland
• PMID: 27231091 (Publication Type: Journal Article)
• Copyright: Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Chemical References

• Analgesics
• Cyclohexane Monoterpenes
• Cyclohexenes
• Monoterpenes
• Receptors, Opioid, delta
• Receptors, Opioid, kappa
• Receptors, Opioid, mu
• beta-Cyclodextrins
• alpha-terpineol
• Naloxone
• Ondansetron
• betadex

Topics

• Analgesics (pharmacology)
• Animals
• Behavior, Animal (drug effects)
• Binding Sites
• Cyclohexane Monoterpenes
• Cyclohexenes (chemistry, pharmacology, therapeutic use)
• Disease Models, Animal
• Fibromyalgia (drug therapy, metabolism, pathology)
• Hyperalgesia (chemically induced, drug therapy, pathology)
• Male
• Mice
• Molecular Docking Simulation
• Monoterpenes (chemistry, pharmacology, therapeutic use)
• Naloxone (pharmacology)
• Ondansetron (pharmacology)
• Protein Structure, Tertiary
• Receptors, Opioid, delta (chemistry, metabolism)
• Receptors, Opioid, kappa (chemistry, metabolism)
• Receptors, Opioid, mu (chemistry, metabolism)
• beta-Cyclodextrins (chemistry)