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在足底注射右啡烷、氯胺酮或美金刚可减轻福尔马林诱导的行为。

Intraplantar injection of dextrorphan, ketamine or memantine attenuates formalin-induced behaviors.

作者信息

Davidson E M, Carlton S M

机构信息

Department of Anatomy and Neurosciences, Marine Biomedical Institute, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-1069, USA.

出版信息

Brain Res. 1998 Feb 23;785(1):136-42. doi: 10.1016/s0006-8993(97)01396-6.

Abstract

The possible prophylactic effects of local injection of NMDA receptor antagonists that are currently used in humans was investigated in the present study. Intraplantar pretreatment with either 5 mM dextrorphan (DEX), 10 mM memantine (MEM) or 10 mM ketamine (KET) significantly attenuated formalin-induced lifting and licking behaviors, however flinching behavior was not effected. Control experiments indicated that these drug actions could be attributed to local and not systemic effects of the antagonists. We hypothesize that these actions result from blocking NMDA receptors present on unmyelinated sensory axons in the skin. These data suggest that peripheral NMDA receptors contribute to nociceptor activation and can be manipulated to reduce pain of peripheral origin. Since DEX, MEM and KET are currently used in humans and considered clinically safe, they have potential therapeutic value in the treatment of physiologic or pathologic pain states which are induced or maintained by peripheral nociceptor activity. Topical or local application would avoid the side effects that can accompany systemic or intrathecal injection of NMDA antagonists.

摘要

本研究调查了目前用于人类的局部注射NMDA受体拮抗剂的可能预防作用。用5 mM右啡烷(DEX)、10 mM美金刚(MEM)或10 mM氯胺酮(KET)进行足底预处理可显著减轻福尔马林诱导的抬足和舔足行为,但对退缩行为无影响。对照实验表明,这些药物作用可归因于拮抗剂的局部而非全身作用。我们推测,这些作用是由于阻断了皮肤中无髓鞘感觉轴突上存在的NMDA受体所致。这些数据表明,外周NMDA受体参与伤害感受器的激活,可以通过调控来减轻外周源性疼痛。由于DEX、MEM和KET目前已用于人类且被认为临床安全,它们在治疗由外周伤害感受器活动诱导或维持的生理或病理疼痛状态方面具有潜在的治疗价值。局部或 topical应用可避免全身或鞘内注射NMDA拮抗剂可能伴随的副作用。 (注:原文中“Topical”未翻译完整,推测可能是想说“局部的”)

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