Effects of gabapentinoids on responses of primary cultures from rat dorsal root ganglia to inflammatory or somatosensory stimuli.
Analgesics
/ pharmacology
Animals
Capsaicin
/ pharmacology
Female
Gabapentin
/ pharmacology
Ganglia, Spinal
/ drug effects
Inflammation
/ chemically induced
Lipopolysaccharides
/ toxicity
Male
Neuralgia
/ drug therapy
Neurons
/ drug effects
Pregabalin
/ pharmacology
Primary Cell Culture
Rats
Rats, Wistar
Sensory System Agents
/ pharmacology
Somatosensory Cortex
/ drug effects
calcium imaging
cytokines
dorsal root ganglia
gabapentinoids
lipopolysaccharide
Journal
Journal of basic and clinical physiology and pharmacology
ISSN: 2191-0286
Titre abrégé: J Basic Clin Physiol Pharmacol
Pays: Germany
ID NLM: 9101750
Informations de publication
Date de publication:
20 Feb 2020
20 Feb 2020
Historique:
received:
10
09
2019
accepted:
26
11
2019
pubmed:
23
2
2020
medline:
1
5
2021
entrez:
21
2
2020
Statut:
epublish
Résumé
Background Gabapentinoids are known to reduce neuropathic pain. The aim of this experimental study was to investigate whether gabapentinoids exert anti-inflammatory and/or anti-nociceptive effects at the cellular level using primary cultures of rat dorsal root ganglia (DRG). Methods Cells from rat DRG were cultured in the presence of gabapentin or pregabalin, and we tested the effects of subsequent stimulation with lipopolysaccharide (LPS) on the expression of genes (real-time polymerase chain reaction) and production of tumor necrosis factor-α (TNFα) and interleukin-6 (IL-6) by specific bioassays. Using Ca2+ imaging, we further investigated in neurons the effects of gabapentinoids upon stimulation with the TRPV-1 agonist capsaicin. Results There is a small influence of gabapentinoids on the inflammatory response to LPS stimulation, namely, a significantly reduced expression of IL-6. Pregabalin and gabapentin further seem to exert a moderate inhibitory influence on capsaicin-induced Ca2+ signals in DRG neurons. Conclusions Although the single inhibitory effects of gabapentinoids on inflammatory and nociceptive responses are moderate, a combination of both effects might provide an explanation for the proposed function of these substances as an adjuvant for the reduction of neuropathic pain.
Identifiants
pubmed: 32078575
doi: 10.1515/jbcpp-2019-0261
pii: /j/jbcpp.ahead-of-print/jbcpp-2019-0261/jbcpp-2019-0261.xml
doi:
pii:
Substances chimiques
Analgesics
0
Lipopolysaccharides
0
Sensory System Agents
0
Pregabalin
55JG375S6M
Gabapentin
6CW7F3G59X
Capsaicin
S07O44R1ZM
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM