Effect of carbamazepine on tetrodotoxin-resistant Na⁺ channels in trigeminal ganglion neurons innervating to the dura.
10.4196/kjpp.2018.22.6.649
- Author:
Jin Eon HAN
1
;
Jin Hwa CHO
;
Michiko NAKAMURA
;
Maan Gee LEE
;
Il Sung JANG
Author Information
1. Department of Pharmacology, School of Dentistry, Kyungpook National University, Daegu 41940, Korea. jis7619@knu.ac.kr
- Publication Type:Original Article
- Keywords:
Carbamazepine;
Dural afferent neurons;
Migraine;
Patch clamp;
Sodium channel;
Tetrodotoxin-resistant
- MeSH:
Action Potentials;
Animals;
Anticonvulsants;
Carbamazepine*;
Headache;
Kinetics;
Migraine Disorders;
Nervous System Diseases;
Neurons*;
Neurons, Afferent;
Rats;
Sodium Channels;
Trigeminal Ganglion*
- From:The Korean Journal of Physiology and Pharmacology
2018;22(6):649-660
- CountryRepublic of Korea
- Language:English
-
Abstract:
Migraine is a neurological disorder characterized by recurrent and disabling severe headaches. Although several anticonvulsant drugs that block voltage-dependent Na⁺ channels are widely used for migraine, far less is known about the therapeutic actions of carbamazepine on migraine. In the present study, therefore, we characterized the effects of carbamazepine on tetrodotoxin-resistant (TTX-R) Na⁺ channels in acutely isolated rat dural afferent neurons, which were identified by the fluorescent dye DiI. The TTX-R Na⁺ currents were measured in medium-sized DiIpositive neurons using the whole-cell patch clamp technique in the voltage-clamp mode. While carbamazepine had little effect on the peak amplitude of transient Na⁺ currents, it strongly inhibited steady-state currents of transient as well as persistent Na⁺ currents in a concentration-dependent manner. Carbamazepine had only minor effects on the voltage-activation relationship, the voltage-inactivation relationship, and the use-dependent inhibition of TTX-R Na⁺ channels. However, carbamazepine changed the inactivation kinetics of TTX-R Na⁺ channels, significantly accelerating the development of inactivation and delaying the recovery from inactivation. In the current-clamp mode, carbamazepine decreased the number of action potentials without changing the action potential threshold. Given that the sensitization of dural afferent neurons by inflammatory mediators triggers acute migraine headaches and that inflammatory mediators potentiate TTX-R Na⁺ currents, the present results suggest that carbamazepine may be useful for the treatment of migraine headaches.
