Literature DB >> 24032674

HDAC inhibitors restore C-fibre sensitivity in experimental neuropathic pain model.

Yosuke Matsushita1, Kohei Araki, Olaposi idowu Omotuyi, Takehiro Mukae, Hiroshi Ueda.   

Abstract

BACKGROUND AND
PURPOSE: Hypoesthesia is a clinical feature of neuropathic pain. The feature is partly explained by the evidence of epigenetic repression of Nav 1.8 sodium channel in the dorsal root ganglion (DRG). EXPERIMENTAL APPROACH: We investigated the possibility of trichostatin A (TSA), valproic acid (VPA) and suberoylanilide hydroxamic acid (SAHA) to reverse the unique C-fibre sensitivity observed following partial ligation of sciatic nerve in mice. KEY
RESULTS: Nerve injury-induced down-regulation of DRG Nav 1.8 sodium channel and C-fibre-related hypoesthesia were reversed by TSA, VPA and SAHA treatments, which inhibit histone deacetylase (HDAC), and increase histone acetylation at the regulatory sequence of Nav 1.8. CONCLUSIONS AND IMPLICATIONS: Taken together, these studies provide the evidence that hypoesthesia and underlying down-regulation of Nav 1.8, negative symptoms observed in nerve injury-induced neuropathic pain models are regulated by an epigenetic chromatin remodelling through HDAC-related machineries.
© 2013 The British Pharmacological Society.

Entities:  

Keywords:  HDAC inhibitor; Nav1.8; epigenetics; hypoesthesia; neuropathic pain

Mesh:

Substances:

Year:  2013        PMID: 24032674      PMCID: PMC3949648          DOI: 10.1111/bph.12366

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


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