Prommer Eric E
Department of Hematology/Oncology/Palliative Care, Mayo Clinic, Phoenix, Arizona, USA.
J Opioid Manag. 2010 May-Jun;6(3):223-6. doi: 10.5055/jom.2010.0020.
Tapentadol hydrochloride (17(-)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol) is a newly released analgesic that works at two levels: by acting as a p-opioid agonist and as a modulator of descending inhibitory pathways through its effects on neurotransmitters involved in these pathways. The theoretical advantage is the provision of synergistic analgesic activities, which may lessen the need for opioid escalation. The advantage is its potential as a possible new agent in neuropathic pain. Preclinical models confirm analgesic properties in acute pain and neuropathic pain models, but with less potency than morphine. Tapentadol has minimal CYP 450 interactions limiting potential for drug interactions. Human clinical trial data in nonmalignant pain suggest less potency than a step-3 opioid, and the drug remains to be tested in patients with cancer pain and neuropathic pain.
盐酸曲马多(17(-)-(1R,2R)-3-(3-二甲基氨基-1-乙基-2-甲基丙基)-苯酚)是一种新上市的镇痛药,其作用于两个层面:作为μ-阿片受体激动剂,并通过对这些途径中涉及的神经递质的作用,作为下行抑制途径的调节剂。理论优势在于提供协同镇痛活性,这可能减少阿片类药物剂量增加的需求。其优势在于它有可能成为治疗神经性疼痛的新型药物。临床前模型证实了其在急性疼痛和神经性疼痛模型中的镇痛特性,但效力低于吗啡。曲马多与细胞色素P450的相互作用极小,限制了药物相互作用的可能性。非恶性疼痛的人体临床试验数据表明其效力低于三级阿片类药物,该药物仍有待在癌症疼痛和神经性疼痛患者中进行测试。