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电针联合MK-801可延长外周炎症大鼠的抗痛觉过敏时间。

Electroacupuncture combined with MK-801 prolongs anti-hyperalgesia in rats with peripheral inflammation.

作者信息

Zhang Rui-Xin, Wang Linbo, Wang Xiaoya, Ren Ke, Berman Brian M, Lao Lixing

机构信息

Center for Integrative Medicine, School of Medicine, University of Maryland, Baltimore, MD 21201, USA.

出版信息

Pharmacol Biochem Behav. 2005 May;81(1):146-51. doi: 10.1016/j.pbb.2005.03.002. Epub 2005 Apr 25.

Abstract

Our previous study showed that electroacupuncture (EA), an adjuvant to conventional medicine, significantly attenuated hyperalgesia in a rat model of inflammatory pain. In the present study, we evaluated the potential additive and/or synergism of EA and a sub-effective dose of dizocilpine maleate (MK-801), a non-competitive N-methyl-d-aspartate (NMDA) receptor antagonist, on hyperalgesia in the same rat model of inflammatory pain. Hyperalgesia, manifesting as decreased paw withdrawal latency (PWL) to a noxious stimulus, was induced by injecting complete Freund's adjuvant (CFA) into the plantar surface of one hind paw of each rat. EA treatments were given at acupoint GB30 immediately after and 2 h after CFA. MK-801 at 0.001 mg/rat was given (i.t.) 10 min before each of the two EA treatments. PWL was measured prior to and 2.5 and 5 h post-CFA. Ten and 100 Hz EA significantly inhibited CFA-induced hind paw hyperalgesia. Both 10 and 100 Hz EA combined with the sub-effective dose of 0.001 mg/rat MK-801 showed prolonged anti-hyperalgesia with no side effects. These results demonstrate that EA combined with a sub-effective dose of this NMDA receptor antagonist enhances anti-hyperalgesia, and this combination may provide an effective strategy for pain management.

摘要

我们之前的研究表明,作为传统医学辅助手段的电针(EA)可显著减轻炎症性疼痛大鼠模型中的痛觉过敏。在本研究中,我们评估了EA与亚有效剂量的马来酸氯氮平(MK-801,一种非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂)在同一炎症性疼痛大鼠模型中对痛觉过敏的潜在相加和/或协同作用。通过向每只大鼠的一只后爪足底注射完全弗氏佐剂(CFA)来诱导痛觉过敏,表现为对有害刺激的爪退缩潜伏期(PWL)缩短。在注射CFA后立即和2小时后于穴位GB30进行EA治疗。在两次EA治疗前10分钟给予0.001mg/大鼠的MK-801(经皮内注射)。在CFA注射前以及注射后2.5和5小时测量PWL。10Hz和100Hz的EA均显著抑制CFA诱导的后爪痛觉过敏。10Hz和100Hz的EA与0.001mg/大鼠的亚有效剂量MK-801联合使用均显示出延长的抗痛觉过敏作用且无副作用。这些结果表明,EA与这种NMDA受体拮抗剂的亚有效剂量联合使用可增强抗痛觉过敏作用,并且这种联合可能为疼痛管理提供一种有效的策略。

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