Evidence that nitric oxide-glutamate cascade modulates spinal antinociceptive effect of morphine: a behavioural and microdialysis study in rats

被引:33
作者
Watanabe, C
Okuda, K
Sakurada, C
Ryuichiro, A
Sakurada, T
Sakurada, S
机构
[1] Daiichi Coll Pharmaceut Sci, Dept Biochem, Minami Ku, Fukuoka 8158511, Japan
[2] Tohoku Pharmaceut Univ, Ctr Lab Anim Sci, Aoba Ku, Sendai, Miyagi 9818558, Japan
[3] Tohoku Pharmaceut Univ, Dept Anat & Pathol, Aoba Ku, Sendai, Miyagi 9818558, Japan
[4] Mogi Hosp, Dept Internal Med, Nishi Ku, Fukuoka 8190002, Japan
关键词
nitric oxide; glutamate; L-NAME; morphine; intrathecal injection; antinociception; spinal cord;
D O I
10.1016/S0006-8993(03)03440-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We evaluated the ability of spinally administered nitric oxide (NO) synthase inhibitor to modulate antinociceptive action of intrathecal (i.t.) morphine in rats by measuring the early and late phases of flinching and licking/biting in the formalin test. To determine the contribution of spinal NO and glutamate, we measured the release of NO metabolites (nitrite/nitrate) and glutamate from the spinal cord in rats, using a microdialysis probe placed in the lumbar space. The i.t. administration of N-G-nitro L-arginine methyl ester (L-NAME) produced a dose-dependent reduction in the number of flinches during the late phase, whereas there were no significant alterations in the late phase licking/ biting, and early phase flinching and licking/biting. Spinal administration of morphine at low doses produced a significant antinociceptive activity in the early and late phases of the flinching behaviour, whereas higher doses of morphine were required to obtain a significant effect in the licking/biting behaviour during both phases. Combination Of L-NAME with morphine resulted in an enhanced reduction in the early and late phase flinching. Enhanced antinociceptive activity was observed in the late phase licking/biting by i.t. combined administration of L-NAME (400 nmol) and morphine (1.25 nmol). In the present study, we have confirmed our prior results that injection of formalin (5.0%) into the plantar surface of the paw evoked a biphasic spinal release of nitrite/nitrate and a transient release of glutamate. Formalin-evoked release of nitrite/nitrate and glutamate was also reduced markedly by i.t. combined administration Of L-NAME and morphine. These behavioural and biochemical results suggest that i.t. administered L-NAME may enhance morphine-induced antinociception through an increased inhibition of nitrite/nitrate and glutamate releases evoked by formalin injection at the spinal cord level. (C) 2003 Elsevier B.V. All rights reserved.
引用
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页码:77 / 86
页数:10
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