Varicella zoster virus induces neuropathic changes in rat dorsal root ganglia and behavioral reflex sensitisation that is attenuated by gabapentin or sodium channel blocking drugs

被引:104
作者
Garry, EM
Delaney, A
Anderson, HA
Sirinathsinghji, EC
Clapp, RH
Martin, WJ
Kinchington, PR
Krah, DL
Abbadie, C
Fleetwood-Walker, SM [1 ]
机构
[1] Univ Edinburgh, Ctr Res Neurosci, Div Vet Biomed Sci, Edinburgh EH9 1QH, Midlothian, Scotland
[2] Merck Res Labs, Dept Pharmacol, Rahway, NJ 07065 USA
[3] Univ Pittsburgh, Dept Ophthalmol, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Dept Mol Genet & Biochem, Pittsburgh, PA 15213 USA
[5] Merck Res Labs, Vaccine & Biol Res, West Point, PA 19486 USA
基金
英国惠康基金;
关键词
post-herpetic neuralgia; varicella zoster virus; dorsal root ganglia; sodium channels; neuropeptide Y; galanin; gabapentin;
D O I
10.1016/j.pain.2005.08.003
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Reactivation of latent varicella zoster virus (VZV) within sensory trigerninal and dorsal root ganglia (DRG) neurons produces shingles (zoster), often accompanied by a chronic neuropathic pain state, post-herpetic neuralgia (PHN). PHN persists despite latency of the virus within human sensory ganglia and is often unresponsive to current analgesic or antiviral agents. To study the basis of varicella zoster-induced pain, we have utilised a recently developed model of chronic VZV infection in rodents. lmmunohistochemical analysis of DRG following VZV infection showed the presence of a viral immediate early gene protein (IE62) co-expressed with markers of A- (neurofilament-200; NF-200) and C- (peripherin) afferent sensory neurons. There was increased expression of neuropeptide Y (NPY) in neurons co-expressing NF-200. In addition, there was an increased expression of alpha 2 delta 1 calcium channel, Na(v)1.3 and Na(v)1.8 sodium channels, the neuropeptide galanin and the nerve injury marker, Activating Transcription Factor-3 (ATF-3) as determined by Western blotting in DRG of VZV-infected rats. VZV infection induced increased behavioral reflex responsiveness to both noxious thermal and mechanical stimuli ipsilateral to injection (lasting up to 10 weeks post-infection) that is mediated by spinal NMDA receptors. These changes were reversed by systemic administration of gabapentin or the sodium channel blockers, mexiletine and lamotrigine, but not by the non-steroidal anti-inflammatory agent, diclofenac. This is the first time that the profile of VZV infection-induced phenotypic changes in DRG has been shown in rodents and reveals that this profile appears to be broadly similar (but not identical) to changes in other neuropathic pain models. (c) 2005 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:97 / 111
页数:15
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