Abstract
Abnormal neural activity generated at a site of nerve injury is thought to contribute to the development of dysaesthesia. Vanilloid receptor 1 (TRPV1), a transducer of noxious stimuli, may be involved in the initiation of this abnormal activity and could provide a useful therapeutic target. We investigated the effect of a specific TRPV1 antagonist (SB-750364) on injury-induced discharge in the lingual nerve. In 12 anaesthetised adult ferrets the left lingual nerve was sectioned and animals were allowed to recover for 3-7 days. In terminal experiments under general anaesthesia, the nerve was re-exposed and electrophysiological recordings made from spontaneously active axons in fine filaments dissected from the nerve central to both the injury site and the junction with the chorda tympani. SB-750364 was infused via the cephalic vein in order to achieve three increasing but stable systemic blood levels of the compound (0.3, 1.0 and 3.0 μM). Twenty-eight spontaneously active units were studied, with discharge frequencies ranging from 0.02 to 4.9 Hz. There was a significant reduction in spontaneous activity in 17 units (61%) at 1.0 μM or less of SB-750364 (p <0.01; Friedman test with Dunn's multiple comparisons). A further 4 units (14%) showed a significant reduction in activity at 3.0 μM (p <0.01). In the remaining 7 units (25%) the discharge was unaffected (p > 0.05). These data show that the TRPV1 antagonist SB-750364 can reduce the level of spontaneous activity initiated in some axons following lingual nerve injury. © 2008 Elsevier Ireland Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 41-45 |
Number of pages | 4 |
Journal | Neuroscience letters |
Volume | 443 |
Issue number | 1 |
DOIs | |
Publication status | Published - 26 Sept 2008 |
Keywords
- Dysaesthesia
- Ectopic activity
- Lingual nerve injury
- Neuropathic pain
- Trigeminal