Webster Lynn R
Lifetree Clinical Research and Pain Clinic, Salt Lake City, Utah, USA.
Expert Opin Investig Drugs. 2007 Aug;16(8):1277-83. doi: 10.1517/13543784.16.8.1277.
Oxytrex (Pain Therapeutics, Inc.) is an oral opioid that combines a therapeutic amount of oxycodone with an ultra-low dose of the antagonist naltrexone. Animal data indicate that this combination minimizes the development of physical dependence and analgesic tolerance while prolonging analgesia. Oxytrex is in late-stage clinical development by Pain Therapeutics for the treatment of moderate-to-severe chronic pain. To evaluate the safety and efficacy of the oxycodone/naltrexone combination, three clinical studies have been conducted, one in healthy volunteers and the other two in patients with chronic pain. The putative mechanism of ultra-low-dose naltrexone is to prevent an alteration in G-protein coupling by opioid receptors that is associated with opioid tolerance and dependence. Opioid agonists are initially inhibitory but become excitatory through constant opioid receptor activity. The agonist/antagonist combination of Oxytrex may reduce the conversion from an inhibitory to an excitatory receptor, thereby decreasing the development of tolerance and physical dependence.
奥昔曲肽(Pain Therapeutics公司)是一种口服阿片类药物,它将治疗剂量的羟考酮与超低剂量的拮抗剂纳曲酮相结合。动物数据表明,这种组合在延长镇痛时间的同时,能将身体依赖性和镇痛耐受性的发展降至最低。奥昔曲肽正处于Pain Therapeutics公司治疗中重度慢性疼痛的后期临床开发阶段。为评估羟考酮/纳曲酮组合的安全性和有效性,已开展了三项临床研究,一项针对健康志愿者,另外两项针对慢性疼痛患者。超低剂量纳曲酮的推测机制是防止阿片受体的G蛋白偶联发生改变,而这种改变与阿片耐受性和依赖性相关。阿片激动剂最初具有抑制作用,但通过持续的阿片受体活性会变为兴奋作用。奥昔曲肽的激动剂/拮抗剂组合可能会减少从抑制性受体向兴奋性受体的转变,从而减少耐受性和身体依赖性的发展。