Peuckmann V, Strumpf M, Zenz M, Bruera E
Klinik für Anaesthesiologie, Intensiv- und Schmerztherapie, Universitätsklinik Bergmannsheil Bochum.
Schmerz. 2003 Jun;17(3):204-10. doi: 10.1007/s00482-003-0216-z.
Thalidomide was introduced as a sedative and antiemetic agent to the European market in the late 1950s. However, it soon became clear that a hitherto unheard-of incidence of severe birth defects was due to the maternal use of thalidomide and the drug was withdrawn from the market. Despite its teratogenesis, thalidomide is currently being rediscovered because of its known spectrum of anticachectic, antiemetic, mildly hypnotic, anxiolytic, anti-inflammatory, antiangiogenic, and analgesic properties. The mechanism of action of thalidomide is probably based on its immunomodulatory effect, namely the suppression of production of tumor necrosis factor alpha and the modulation of interleukins. A striking but not well-known finding is the effectiveness of thalidomide as an analgesic or analgesic adjuvant. During the early era of thalidomide use, the drug was shown to enhance the analgesic efficacy of a combined treatment with acetylsalicylic acid, phenacetin, and caffeine (APC) by testing "normal volunteers, using electrical stimulation of teeth." The combination of thalidomide and APC was superior to other combinations (APC alone, APC and codeine) with respect to both the total analgesic effect and the duration of this analgesic effect. In 1965 thalidomide was found to be effective in treating the painful subcutaneous manifestations of the leprosy-associated erythema nodosum leprosum, a condition for which it eventually was approved by the United States Food and Drug Administration in 1998. In an animal model of neuropathic pain (chronic constriction injury), thalidomide was shown to reduce both mechanical allodynia and thermal hyperalgesia. Recent studies documented the analgesic efficacy of thalidomide in treating painful mucocutaneous aphthous ulcers associated with HIV syndrome and Behcet's disease.However, to date there are no recent clinical trials that are specifically designed to explore the analgesic potential of thalidomide. In view of the current basic research and clinical findings,we suggest to investigate the potential benefits of thalidomide in severe pain conditions that respond poorly to common pain management approaches such as neuropathic pain, postherpetic neuralgia, or central pain phenomena. Because its mechanism of action is distinct from that of other drugs such as steroids, thalidomide offers the possibility of a combined treatment with other agents with nonoverlapping toxicities. We conclude that thalidomide, when used properly,may enrich the therapeutic regimen in the management of some pain-related conditions.
沙利度胺于20世纪50年代末作为一种镇静和止吐药物被引入欧洲市场。然而,很快就发现,孕妇使用沙利度胺导致了一种前所未有的严重出生缺陷发生率,该药物因此被撤出市场。尽管具有致畸性,但由于其已知的抗恶病质、止吐、轻度催眠、抗焦虑、抗炎、抗血管生成和镇痛特性,沙利度胺目前正在被重新发现。沙利度胺的作用机制可能基于其免疫调节作用,即抑制肿瘤坏死因子α的产生和调节白细胞介素。一个显著但鲜为人知的发现是沙利度胺作为一种镇痛药或镇痛辅助药物的有效性。在沙利度胺使用的早期,通过对“正常志愿者进行牙齿电刺激测试”表明,该药物可增强乙酰水杨酸、非那西丁和咖啡因(APC)联合治疗的镇痛效果。沙利度胺与APC的组合在总镇痛效果和镇痛效果持续时间方面均优于其他组合(单独使用APC、APC与可待因)。1965年发现沙利度胺对治疗与麻风相关的结节性红斑的疼痛性皮下表现有效,该病症最终于1998年被美国食品药品监督管理局批准使用。在神经性疼痛(慢性压迫损伤)的动物模型中,沙利度胺被证明可减轻机械性异常性疼痛和热痛觉过敏。最近的研究记录了沙利度胺在治疗与HIV综合征和白塞病相关的疼痛性黏膜皮肤阿弗他溃疡方面的镇痛效果。然而,迄今为止,尚无专门设计用于探索沙利度胺镇痛潜力的近期临床试验。鉴于当前的基础研究和临床发现,我们建议研究沙利度胺在对常见疼痛管理方法(如神经性疼痛、带状疱疹后神经痛或中枢性疼痛现象)反应不佳的严重疼痛状况中的潜在益处。由于其作用机制与其他药物(如类固醇)不同,沙利度胺提供了与其他具有非重叠毒性的药物联合治疗的可能性。我们得出结论,沙利度胺在正确使用时,可能会丰富某些疼痛相关病症管理中的治疗方案。