Vocci Frank J, Acri Jane, Elkashef Ahmed
Division of Pharmacotherapies and Medical Consequences of Drug Abuse, 6001 Executive Blvd., Rm. 4133, MSC 9551, Bethesda, MD 20892-9551, USA.
Am J Psychiatry. 2005 Aug;162(8):1432-40. doi: 10.1176/appi.ajp.162.8.1432.
In 1989, the National Institute on Drug Abuse (NIDA) established its Medications Development Program. This program has concentrated on developing pharmacotherapies for opiate and cocaine dependence and, more recently, for methamphetamine and cannabis dependence. The major goals of this program are to optimize existing treatments and to expand treatment options for physicians and patients. This review will concentrate on the development of pharmacotherapies for the following substance abuse disorders: opiate, cocaine, methamphetamine, and cannabis dependence. Left untreated, opiate and stimulant dependence are responsible for significant morbidity and mortality. For example, use of illicit opiates is associated with an increased risk of hepatitis C infection, HIV infection, and other medical consequences, e.g., an overdose. The NIDA Medications Development Program has had success in developing, with pharmaceutical partners, levomethadyl acetate, buprenorphine, and buprenorphine/naloxone for opiate dependence. Moreover, several marketed medications have shown promise in reducing cocaine use. Of interest, these medications likely operate through diverse neurochemical mechanisms, suggesting that combination therapy may be a rational next step that could increase treatment gains further in cocaine-dependent patients. The Medications Development Program has also identified multiple neuronal mechanisms that are altered by chronic administration of drugs of abuse. Advances in neuroscience have identified changes in conditioned cueing, drug priming, stress-induced increases in drug intake, and reduced frontal inhibitory mechanisms as all being possible for the development of, maintenance of, and possible relapse to, addiction. Potential medications that modulate these mechanisms are highlighted.
1989年,美国国家药物滥用研究所(NIDA)设立了药物研发项目。该项目专注于开发针对阿片类药物和可卡因成瘾的药物治疗方法,最近还涉及甲基苯丙胺和大麻成瘾的治疗。该项目的主要目标是优化现有治疗方法,并为医生和患者拓展治疗选择。本综述将聚焦于以下药物滥用障碍的药物治疗开发:阿片类药物、可卡因、甲基苯丙胺和大麻成瘾。若不进行治疗,阿片类药物和兴奋剂成瘾会导致严重的发病率和死亡率。例如,使用非法阿片类药物会增加丙型肝炎感染、艾滋病毒感染以及其他医疗后果的风险,如用药过量。NIDA药物研发项目与制药合作伙伴成功开发出了用于治疗阿片类药物成瘾的醋酸左美沙朵、丁丙诺啡和丁丙诺啡/纳洛酮。此外,几种已上市的药物在减少可卡因使用方面显示出了前景。有趣的是,这些药物可能通过多种神经化学机制发挥作用,这表明联合治疗可能是合理的下一步措施,有望进一步提高可卡因成瘾患者的治疗效果。药物研发项目还确定了因长期滥用药物而改变的多种神经元机制。神经科学的进展表明,条件性提示、药物启动、压力诱导的药物摄入量增加以及额叶抑制机制减弱等变化,都可能导致成瘾的形成、维持以及可能的复发。文中强调了调节这些机制的潜在药物。