Literature DB >> 19372353

The effect of amitriptyline on ectopic discharge of primary afferent fibers in the L5 dorsal root in a rat model of neuropathic pain.

Xin Su1, Annie H Liang, Mark O Urban.   

Abstract

BACKGROUND: The sodium channel blocker amitriptyline has been shown to inhibit ectopic discharge in injured nerves. In the present study, we characterized ectopic discharges of afferent fibers following L5/L6 spinal nerve ligation (SNL) by their electrophysiological properties and sensitivities to inhibition by amitriptyline in the decentralized L5 dorsal root in SNL rats.
METHODS: Rats exhibiting withdrawal thresholds <4.0 g after SNL were selected for the present study. After laminectomy in pentobarbital-anesthetized rats, the L5 dorsal root was decentralized close to its entry to the spinal cord, and the spontaneous activities of single units were recorded peripherally before and after IV administration of amitriptyline. The mean frequency of afferent fiber activity and instantaneous frequency were measured.
RESULTS: The spontaneous activities of afferent fibers in naïve rats had high frequency (35.23 +/- 6.63 Hz) and pattern discharge based on their instantaneous frequencies and interspike interval distributions. In rats that had received SNL, afferent fibers exhibited spontaneous discharge (mean of 11.05 +/- 3.66 Hz) with an irregular discharge pattern or short bursting activity in some cases. Only 5/13 (38%) afferent fibers from naïve rats showed reduced spontaneous activities after amitriptyline (2 mg/kg, IV), whereas amitriptyline significantly inhibited ectopic discharge in 13/18 (72%) afferent fibers from SNL rats (ID(50) = 1.66 +/- 0.17 mg/kg). Furthermore, the greatest inhibitory effect of amitriptyline was consistently observed on those afferent fibers exhibiting low frequency (<20 Hz) and/or bursting discharge.
CONCLUSION: These results provide direct evidence that amitriptyline, which is used clinically for the treatment of neuropathic pain, selectively inhibits ectopic discharge of low frequency and bursting discharge in the rat neuropathic pain model.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19372353     DOI: 10.1213/ane.0b013e31819b0271

Source DB:  PubMed          Journal:  Anesth Analg        ISSN: 0003-2999            Impact factor:   5.108


  4 in total

1.  Amitriptyline does not block the action of ATP at human P2X4 receptor.

Authors:  J A Sim; R A North
Journal:  Br J Pharmacol       Date:  2010-03-19       Impact factor: 8.739

2.  In vivo and ex vivo inhibition of spinal nerve ligation-induced ectopic activity by sodium channel blockers correlate to in vitro inhibition of NaV1.7 and clinical efficacy: a pharmacokinetic-pharmacodynamic translational approach.

Authors:  Ivana Kalezic; Lei Luo; Per-Eric Lund; Anders B Eriksson; Tjerk Bueters; Sandra A G Visser
Journal:  Pharm Res       Date:  2013-02-01       Impact factor: 4.200

3.  Pretreatment with intrathecal amitriptyline potentiates anti-hyperalgesic effects of post-injury intra-peritoneal amitriptyline following spinal nerve ligation.

Authors:  Kuang-I Cheng; Hung-Chen Wang; Lin-Li Chang; Fu-Yen Wang; Chung-Sheng Lai; Chao-Wen Chou; Hung-Pei Tsai; Aij-Lie Kwan
Journal:  BMC Neurol       Date:  2012-06-21       Impact factor: 2.474

4.  Contact hypersensitivity to oxazolone provokes vulvar mechanical hyperalgesia in mice.

Authors:  Tijana Martinov; Rose Glenn-Finer; Sarah Burley; Elena Tonc; Evelyn Balsells; Alyssa Ashbaugh; Linnea Swanson; Randy S Daughters; Devavani Chatterjea
Journal:  PLoS One       Date:  2013-10-25       Impact factor: 3.240

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.