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Upregulation of Nav1.7 by endogenous hydrogen sulfide contributes to maintenance of neuropathic pain
- Source :
- International Journal of Molecular Medicine
- Publication Year :
- 2020
- Publisher :
- D.A. Spandidos, 2020.
-
Abstract
- Nav1.7 is closely associated with neuropathic pain. Hydrogen sulfide (H2S) has recently been reported to be involved in numerous biological functions, and it has been shown that H2S can enhance the sodium current density, and inhibiting the endogenous production of H2S mediated by cystathionine β-synthetase (CBS) using O-(carboxymethyl) hydroxylamine hemihydrochloride (AOAA) can significantly reduce the expression of Nav1.7 and thus the sodium current density in rat dorsal root ganglion (DRG) neurons. In the present study, it was shown that the fluorescence intensity of H2S was increased in a spared nerve injury (SNI) model and AOAA inhibited this increase. Nav1.7 is expressed in DRG neurons, and the expression of CBS and Nav1.7 were increased in DRG neurons 7, 14 and 21 days post-operation. AOAA inhibited the increase in the expression of CBS, phosphorylated (p)-MEK1/2, p-ERK1/2 and Nav1.7 induced by SNI, and U0126 (a MEK blocker) was able to inhibit the increase in p-MEK1/2, p-ERK1/2 and Nav1.7 expression. However, PF-04856264 did not inhibit the increase in CBS, p-MEK1/2, p-ERK1/2 or Nav1.7 expression induced by SNI surgery. The current density of Nav1.7 was significantly increased in the SNI model and administration of AOAA and U0126 both significantly decreased the density. In addition, AOAA, U0126 and PF-04856264 inhibited the decrease in rheobase, and the increase in action potential induced by SNI in DRG neurons. There was no significant difference in thermal withdrawal latency among each group. However, the time the animals spent with their paw lifted increased significantly following SNI, and the time the animals spent with their paw lifted decreased significantly following the administration of AOAA, U0126 and PF-04856264. In conclusion, these data show that Nav1.7 expression in DRG neurons is upregulated by CBS-derived endogenous H2S in an SNI model, contributing to the maintenance of neuropathic pain.
- Subjects :
- 0301 basic medicine
Male
medicine.medical_specialty
SNi
dorsal root ganglion
hydrogen sulfide
Endogeny
Rats, Sprague-Dawley
03 medical and health sciences
0302 clinical medicine
Dorsal root ganglion
Downregulation and upregulation
Internal medicine
Genetics
medicine
Animals
Extracellular Signal-Regulated MAP Kinases
Nav1.7
neuropathic pain
Mitogen-Activated Protein Kinase Kinases
cystathionine β-synthetase
biology
Chemistry
NAV1.7 Voltage-Gated Sodium Channel
General Medicine
Articles
Nerve injury
Cystathionine beta synthase
Rats
Up-Regulation
030104 developmental biology
Rheobase
Endocrinology
medicine.anatomical_structure
030220 oncology & carcinogenesis
Neuropathic pain
biology.protein
Neuralgia
medicine.symptom
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 1791244X and 11073756
- Volume :
- 46
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- International Journal of Molecular Medicine
- Accession number :
- edsair.doi.dedup.....450a85c7947451f8aba4b34c89c9b369