Involvement of nuclear factor κB and descending pain pathways in the anti-hyperalgesic effect of β-citronellol, a food ingredient, complexed in β-cyclodextrin in a model of complex regional pain syndrome - Type 1.
Acyclic Monoterpenes
/ therapeutic use
Analgesics
/ therapeutic use
Animals
Anti-Inflammatory Agents
/ therapeutic use
Cyclooxygenase 2
/ metabolism
Drug Carriers
/ chemistry
Food Ingredients
Hyperalgesia
/ drug therapy
Male
Mice
NF-kappa B p50 Subunit
/ metabolism
Reflex Sympathetic Dystrophy
/ drug therapy
Spinal Cord Dorsal Horn
/ drug effects
Tumor Necrosis Factor-alpha
/ metabolism
beta-Cyclodextrins
/ chemistry
Chronic Pain
Citronellol
Complex regional pain syndrome
Cyclodextrin
Monoterpene
Type I
Journal
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association
ISSN: 1873-6351
Titre abrégé: Food Chem Toxicol
Pays: England
ID NLM: 8207483
Informations de publication
Date de publication:
Jul 2021
Jul 2021
Historique:
received:
09
03
2021
revised:
22
04
2021
accepted:
08
05
2021
pubmed:
30
5
2021
medline:
5
10
2021
entrez:
29
5
2021
Statut:
ppublish
Résumé
Complex regional pain syndrome type 1 (CRPS-1) is a painful syndrome without effective treatment. In order to explore possible new treatments, we used an animal model of CRPS-1 to examine the effects of β-Citronellol (βCT), a monoterpene found in a variety of plants that has been shown to have analgesic effects. We aimed to assess its effects alone, and complexed with β-cyclodextrin (βCD), which has been previously used to enhance the effects of a number of medicines. The βCT-βCD was characterized physiochemically using high performance liquid chromatography (HPLC) and differential scanning calorimetry (DSC) and shown to have 80% efficiency. In the animal model, Swiss mice were treated with βCT, βCT-βCD, vehicle, pregabalin or sham and evaluated for hyperalgesia and motor coordination. Inflammatory mediators were measured by Western blot or ELISA and the descending pain pathway by immunofluorescence. βCT was shown to have an anti-hyperalgesic effect (without affecting motor coordination) that reduced inflammatory mediators and activated the descending pain pathway, and these effects were increased with complexation in βCD. Our results showed βCT-βCD to be a promising treatment for CRPS-1.
Identifiants
pubmed: 34051299
pii: S0278-6915(21)00293-3
doi: 10.1016/j.fct.2021.112260
pii:
doi:
Substances chimiques
Acyclic Monoterpenes
0
Analgesics
0
Anti-Inflammatory Agents
0
Drug Carriers
0
Food Ingredients
0
NF-kappa B p50 Subunit
0
Tumor Necrosis Factor-alpha
0
beta-Cyclodextrins
0
Nfkb1 protein, mouse
147257-52-1
Ptgs2 protein, mouse
EC 1.14.99.-
Cyclooxygenase 2
EC 1.14.99.1
citronellol
P01OUT964K
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
112260Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.