Analgesic action of loperamide, an opioid agonist, and its blocking action on voltage-dependent Ca2+ channels

被引:32
作者
Hagiwara, K
Nakagawasai, O
Murata, A
Yamadera, F
Miyoshi, I
Tan-No, K
Tadano, T
Yanagisawa, T
Iijima, T
Murakami, M
机构
[1] Akita Univ, Sch Med, Dept Pharmacol, Akita 0108543, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Mol Pharmacol, Sendai, Miyagi 9808575, Japan
[3] Tohoku Pharmaceut Univ, Dept Pharmacol, Sendai, Miyagi 9810905, Japan
[4] Tohoku Univ, Grad Sch Med, Inst Anim Expt, Sendai, Miyagi 9808575, Japan
关键词
loperamide; analgesia; calcium channels; DRG neuron; mice; formalin;
D O I
10.1016/S0168-0102(03)00126-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the relationship between the antinociceptive effect of the opiate agonist loperamide at the spinal level and its inhibitory effect on calcium influx. Intrathecal administration of loperamide showed a significant antinociceptive effect in the formalin test, which was not prevented by naloxone. On the other hand, no significant effects were observed by nicardipine, an L-type specific blocker, or by BAY K8644, an L-type specific agonist, suggesting no significant role of L-type calcium channels in nociceptive signal transduction. Loperamide suppressed the calcium influx in dorsal root ganglion neurons. As the antinociceptive effect of loperamide was not affected by naloxone or other calcium channel blocking toxins, and loperamide showed a direct inhibitory effect on calcium-influx, the analgesic effect of intrathecally injected loperamide might be due to its blockade of the volt age-dependent calcium channels at the terminals of the primary afferent fibers. (C) 2003 Elsevier Science Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:493 / 497
页数:5
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