Antidepressants enhance the antinociceptive effects of carbamazepine in the acetic acid-induced writhing test in mice

被引:24
作者
Aoki, Mieko
Tsuji, Minoru
Takeda, Hiroshi
Harada, Yoichiro
Nohara, Jun
Matsumiya, Teruhiko
Chiba, Hiroshige
机构
[1] Tokyo Med Univ, Dept Oral & Maxillofacial Surg, Shinjuku Ku, Tokyo 1600023, Japan
[2] Tokyo Med Univ, Dept Pharmacol, Shinjuku Ku, Tokyo 1608402, Japan
[3] Int Univ Hlth & Welf, Sch Pharmaceut Sci, Div Pharmacol, Ohtawara, Tochigi 3248501, Japan
关键词
imipramine; fluvoxamine; milnacipran; carbamazepine; writhing test; (mouse);
D O I
10.1016/j.ejphar.2006.08.049
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Some antidepressants, as well as antiepileptics, are effective for treating pain of varying etiology. The present study was designed to characterize the antinociceptive effects of imipramine, a tricyclic antidepressant, fluvoxamine, a selective serotonin reuptake inhibitor, milnacipran, a serotonin noradrenaline reuptake inhibitor, and carbamazepine, an antiepileptic drug, using the acetic acid-induced writhing test in mice. Imipramine (1.25-10 mg/kg, i.p.), fluvoxamine (5-40 mg/kg, i.p.) and milnacipran (2.5-20 mg/kg, i.p.) all dose-dependently and significantly reduced the number of writhes induced by the injection of acetic acid (0.8% (v/v)), although the maximal effect of milnacipran was weaker than those of imipramine and fluvoxamine. Similarly, carbamazepine (5-20 mg/kg, i.p.) also showed a dose-dependent and significant antinociceptive effect. In combination studies, the co-administration of a sub-effective dose of carbamazepine (5 mg/kg, i.p.) with imipramine (1.25 and 2.5 mg/kg, i.p.), fluvoxamine (10 mg/kg, i.p.) or milnacipran (1.25 and 2.5 mg/kg, i.p.) significantly reduced the number of writhes. Additionally, the hole-board test revealed that the medications with significant antinociceptive effects barely produced changes in motor activity that could possibly affect writhing behavior. Thus, the present study demonstrated that the antinociceptive effect of carbamazepine is enhanced by combination with imipramine, fluvoxamine and milnacipran. Therefore, the combined therapy using antidepressants and carbamazepine may be useful clinically for the control of pain. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:78 / 83
页数:6
相关论文
共 44 条
[21]   Of histamine H1 receptor in pain perception:: a study of the receptor gene knockout mice [J].
Mobarakeh, JI ;
Sakurada, S ;
Katsuyama, S ;
Kutsuwa, M ;
Kuramasu, A ;
Lin, ZY ;
Watanabe, T ;
Hashimoto, Y ;
Watanabe, T ;
Yanai, K .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2000, 391 (1-2) :81-89
[22]   Serotonin and noradrenaline reuptake inhibitors in animal models of pain [J].
Mochizucki, D .
HUMAN PSYCHOPHARMACOLOGY-CLINICAL AND EXPERIMENTAL, 2004, 19 :S15-S19
[23]   Neurochemical and behavioural characterization of milnacipran, a serotonin and noradrenaline reuptake inhibitor in rats [J].
Mochizuki, D ;
Tsujita, R ;
Yamada, S ;
Kawasaki, K ;
Otsuka, Y ;
Hashimoto, S ;
Hattori, T ;
Kitamura, Y ;
Miki, N .
PSYCHOPHARMACOLOGY, 2002, 162 (03) :323-332
[24]   Interactions between anticonvulsant and psychoactive drugs [J].
Monaco, F ;
Cicolin, A .
EPILEPSIA, 1999, 40 :S71-S76
[25]  
Novakovic SD, 1998, J NEUROSCI, V18, P2174
[26]  
O'Malley PG, 1999, J FAM PRACTICE, V48, P980
[27]   Antinociceptive efficacy of antidepressants: Assessment of five antidepressants and four monoamine receptors in rats [J].
Otsuka N. ;
Kiuchi Y. ;
Yokogawa F. ;
Masuda Y. ;
Oguchi K. ;
Hosoyamada A. .
Journal of Anesthesia, 2001, 15 (3) :154-158
[28]   Pharmacokinetics of milnacipran in comparison with other antidepressants [J].
Puozzo, C ;
Leonard, BE .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1996, 11 :15-27
[29]  
Richelson E, 2003, J CLIN PSYCHIAT, V64, P5
[30]   Antinociceptive effects of tricyclic antidepressants and their noradrenergic metabolites [J].
Rojas-Corrales, MO ;
Casas, J ;
Moreno-Brea, MR ;
Gibert-Rahola, J ;
Micó, JA .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2003, 13 (05) :355-363