A comparison of the anti-nociceptive effects of voltage-activated Na+ channel blockers in the formalin test

被引:48
作者
Blackburn-Munro, G [1 ]
Ibsen, N [1 ]
Erichsen, HK [1 ]
机构
[1] NeuroSearch AS, Dept Pharmacol, DK-2750 Ballerup, Denmark
关键词
formalin test; hyperalgesia; inflammation; ion channels; neuropathic pain;
D O I
10.1016/S0014-2999(02)01765-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have used the rat formalin test to compare the anti-nociceptive properties of several voltage-activated Na+ channel blockers. The antiarrhthymic mexiletine (37.5 and 50 mg/kg, i.p.) attenuated flinching behaviour in both first and second phases of the test compared with vehicle (P < 0.05). The anti-convulsants lamotrigine (15 and 30 mg/kg, i.p.) and carbamazepine (20 mg/kg, i.p.) also inhibited second phase flinching behaviour compared with vehicle (P < 0.05), although phenytoin (up to 40 mg/kg, i.p.) was without effect. Riluzole (5 mg/kg, i.p.), in contrast to lubeluzole (up to 10 mg/kg, i.p.) also inhibited second phase flinching behaviour compared with vehicle (P<0.05). When tested against an acute thermal nociceptive stimulus mexiletine, lubeluzole and riluzole exhibited anti-nociceptive effects. The antinociceptive doses used in the formalin test produced no motor impairment in the rotarod test. Thus, voltage-activated Na+ channel blockers can attenuate nociceptive behaviour in the formalin test, and a specific mechanism of action on Na+ channel function may be required for this to occur. (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:231 / 238
页数:8
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