Antinociceptive effect of paeoniflorin via spinal α2-adrenoceptor activation in diabetic mice

被引:29
作者
Lee, Keiko K. [1 ]
Omiya, Yuji [1 ]
Yuzurihara, Mitsutoshi [1 ]
Kase, Yoshio [1 ]
Kobayashi, Hiroyuki [1 ]
机构
[1] Juntendo Univ, Grad Sch Med, Ctr Adv Kampo Med & Clin Res, Dept Hosp Adm,Bunkyo Ku, Tokyo 1138421, Japan
关键词
Paeoniae radix; Paeoniflorin; Antinociception; alpha(2)-Adrenoceptors; Noradrenaline; SHAKUYAKU-KANZO-TO; ADENOSINE A(1) RECEPTOR; COMBINATION CHEMOTHERAPY; HEMODIALYSIS-PATIENTS; KAMPO MEDICINE; PACLITAXEL; RELEASE; TANG; GAN; CARBOPLATIN;
D O I
10.1016/j.ejpain.2011.04.011
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Background: Shakuyakukanzoto (SKT) has been shown to modulate nociception in streptozotocin-induced diabetic mice via selective activation of the descending noradrenergic systems. However, the active components of SKT that exert the analgesic effect remain unknown. Here, we administered Glycyrrhizae radix (G. radix), Paeoniae radix (P. radix), and the two active constituents of P. radix, paeoniflorin and albiflorin, to determine the components that stimulate spinal alpha(2)-adrenoceptors by promoting noradrenaline release. Methods: The two SKT components were separately administered to diabetic and non-diabetic mice. A tail-pressure test was used to determine the nociceptive threshold between 0 and 3 h after oral dosing. The time-course profiles of the nociceptive threshold (g) and the area under the time response curve (AUC) were evaluated. Yohimbine, an alpha(2)-adrenoceptor antagonist, was intrathecally injected 15 min after paeoniflorin administration. Results: P. radix and G. radix did not induce significant antinociception in non-diabetic mice. However, P. radix (250, 500 mg/kg) dose-dependently and significantly increased the nociceptive threshold in diabetic mice between 0.5 and 2 h after administration, whereas all the tested doses of G. radix did not increase the nociceptive threshold. Both paeoniflorin (30 mg/kg) and albiflorin (10 mg/kg) significantly elevated the nociceptive threshold between 0.5 and 3 h and between 0.5 and 1 h after administration, respectively. The antinociceptive effect of paeoniflorin (30 mg/kg) was completely abolished by yohimbine. Conclusion: Our findings suggest that paeoniflorin is the key antinociceptive component in SKT that increases noradrenaline release and activates alpha(2)-adrenoceptors to modulate spinal nociceptive transmission in diabetic neuropathy. (C) 2011 European Federation of International Association for the Study of Pain Chapters. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1035 / 1039
页数:5
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