哌甲酯治疗可卡因成瘾的临床潜力:对现有证据的回顾。

IF 5.1 Q1 SUBSTANCE ABUSE Substance Abuse and Rehabilitation Pub Date : 2015-06-17 eCollection Date: 2015-01-01 DOI:10.2147/SAR.S50807
Kenneth M Dürsteler, Eva-Maria Berger, Johannes Strasser, Carlo Caflisch, Jochen Mutschler, Marcus Herdener, Marc Vogel
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引用次数: 0

摘要

背景:可卡因使用仍然是一个公共卫生问题,但目前尚无经证实有效的药物治疗可卡因依赖。治疗可卡因依赖的一种有希望的方法可能是激动剂替代疗法,这种疗法已经有效地用于治疗阿片类药物和烟草依赖。可卡因依赖的替代方法假定,服用长效兴奋剂药物应使长期使用可卡因引起的神经化学和行为紊乱正常化。一种可能取代可卡因的药物是哌醋甲酯(MPH),因为这种兴奋剂具有与可卡因相似的药物行为特性。目的:提供一个定性的回顾,解决使用MPH作为可卡因替代品的基本原理及其在治疗可卡因依赖的临床潜力。方法:我们在MEDLINE检索使用MPH治疗可卡因滥用/依赖患者的临床研究,并筛选相关文献的文献书目。结果:MPH与可卡因一样,通过抑制多巴胺再摄取而增加突触多巴胺。MPH和可卡因的鉴别特性、强化电位和主观效应几乎相同,重要的是,在实验室条件下,在动物和人类志愿者中发现MPH可以替代可卡因。然而,当以治疗剂量口服时,其滥用风险似乎很低,对于缓释MPH制剂尤其如此。虽然文献中有一些令人鼓舞的数据,主要来自病例报告和开放标签研究,但迄今为止随机对照试验的结果令人失望,并且不能证实在没有注意缺陷多动障碍的患者中使用MPH作为可卡因依赖的替代品。结论:评价MPH替代可卡因依赖的临床研究提供了不一致的结果。然而,阴性结果可以用特定的研究特征来解释,其中包括剂量、治疗持续时间或样本量。在讨论MPH作为可卡因依赖替代疗法的潜力时,需要考虑到这一点。最后,在此基础上提出了今后可能的研究方向。
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Clinical potential of methylphenidate in the treatment of cocaine addiction: a review of the current evidence.

Background: Cocaine use continues to be a public health problem, yet there is no proven effective pharmacotherapy for cocaine dependence. A promising approach to treating cocaine dependence may be agonist-replacement therapy, which is already used effectively in the treatment of opioid and tobacco dependence. The replacement approach for cocaine dependence posits that administration of a long-acting stimulant medication should normalize the neurochemical and behavioral perturbations resulting from chronic cocaine use. One potential medication to be substituted for cocaine is methylphenidate (MPH), as this stimulant possesses pharmacobehavioral properties similar to those of cocaine.

Aim: To provide a qualitative review addressing the rationale for the use of MPH as a cocaine substitute and its clinical potential in the treatment of cocaine dependence.

Methods: We searched MEDLINE for clinical studies using MPH in patients with cocaine abuse/dependence and screened the bibliographies of the articles found for pertinent literature.

Results: MPH, like cocaine, increases synaptic dopamine by inhibiting dopamine reuptake. The discriminative properties, reinforcing potential, and subjective effects of MPH and cocaine are almost identical and, importantly, MPH has been found to substitute for cocaine in animals and human volunteers under laboratory conditions. When taken orally in therapeutic doses, its abuse liability, however, appears low, which is especially true for extended-release MPH preparations. Though there are promising data in the literature, mainly from case reports and open-label studies, the results of randomized controlled trials have been disappointing so far and do not corroborate the use of MPH as a substitute for cocaine dependence in patients without attention deficit hyperactivity disorder.

Conclusion: Clinical studies evaluating MPH substitution for cocaine dependence have provided inconsistent findings. However, the negative findings may be explained by specific study characteristics, among them dosing, duration of treatment, or sample size. This needs to be considered when discussing the potential of MPH as replacement therapy for cocaine dependence. Finally, based on the results, we suggest possible directions for future research.

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