Chair in Clinical Pharmacology and Therapeutics, University of Hertfordshire, School of Life and Medical Sciences, College Lane Campus, Hatfield, AL10 9AB, UK,
CNS Drugs. 2014 Jun;28(6):491-6. doi: 10.1007/s40263-014-0164-4.
Gabapentinoids (e.g. pregabalin and gabapentin) are widely used in neurology, psychiatry and primary healthcare but are increasingly being reported as possessing a potential for misuse. In fact, increasing levels of both prescriptions and related fatalities, together with an anecdotally growing black market, have been reported from a range of countries. This article reviews the current evidence base of this potential, in an attempt to answer the question of whether there is cause for concern about these drugs. Potent binding of pregabalin/gabapentin at the calcium channel results in a reduction in the release of excitatory molecules. Furthermore, gabapentinoids are thought to possess GABA-mimetic properties whilst possibly presenting with direct/indirect effects on the dopaminergic 'reward' system. Overall, pregabalin is characterized by higher potency, quicker absorption rates and greater bioavailability levels than gabapentin. Although at therapeutic dosages gabapentinoids may present with low addictive liability levels, misusers' perceptions for these molecules to constitute a valid substitute for most common illicit drugs may be a reason of concern. Gabapentinoid experimenters are profiled here as individuals with a history of recreational polydrug misuse, who self-administer with dosages clearly in excess (e.g. up to 3-20 times) of those that are clinically advisable. Physicians considering prescribing gabapentinoids for neurological/psychiatric disorders should carefully evaluate a possible previous history of drug abuse, whilst being able to promptly identify signs of pregabalin/gabapentin misuse and provide possible assistance in tapering off the medication.
加巴喷丁类药物(如普瑞巴林和加巴喷丁)广泛应用于神经病学、精神病学和初级保健领域,但越来越多的报道称它们具有潜在的滥用风险。事实上,越来越多的处方和相关的死亡病例,以及一个传闻中的黑市,已经在许多国家得到了报道。本文综述了这些潜在风险的现有证据基础,试图回答是否有理由担心这些药物的问题。普瑞巴林/加巴喷丁在钙通道上的强结合导致兴奋性分子的释放减少。此外,加巴喷丁类药物被认为具有 GABA 模拟特性,同时可能对多巴胺能“奖励”系统具有直接/间接影响。总体而言,普瑞巴林的效力比加巴喷丁更强,吸收速度更快,生物利用度更高。尽管在治疗剂量下,加巴喷丁类药物可能具有较低的成瘾性,但滥用者认为这些分子可以作为大多数常见非法药物的有效替代品,这可能是一个令人担忧的原因。加巴喷丁类药物的使用者被描绘为有滥用多种药物史的个体,他们自行服用的剂量明显超过临床建议剂量(例如,高达 3-20 倍)。医生在考虑为神经/精神疾病开加巴喷丁类药物时,应仔细评估患者是否有滥用药物的既往史,同时能够及时识别普瑞巴林/加巴喷丁滥用的迹象,并为逐渐减少药物剂量提供可能的帮助。