Rosse R B, Alim T N, Fay-McCarthy M, Collins J P, Vocci F J, Lindquist T, Jentgen C, Hess A L, Deutsch S I
VA/NIDA Substance Abuse Research Unit, Washington, D.C., USA.
Clin Neuropharmacol. 1994 Aug;17(4):348-58. doi: 10.1097/00002826-199408000-00007.
Recent preclinical studies suggest utility for voltage-sensitive calcium channel blockers (VSCCBs) in the treatment of cocaine addiction. The following double-blind placebo-controlled study examined the role of the VSCCB nimodipine in attenuating cocaine craving in 66 recently abstinent cocaine-dependent patients on an inpatient substance abuse treatment unit utilizing an intensive 12-step milieu-oriented psychosocial therapy. While the medication was well tolerated, the dose of nimodipine used in this study (90 mg q.d.) was not superior to placebo in reducing background or cue-induced cocaine craving over the 3 weeks of the study. There was the suggestion that nimodipine might attenuate the severity of some cocaine-induced brain deficits, as detected by evaluation of smooth pursuit eye movement function. A rationale for evaluating higher doses of nimodipine for the treatment of cocaine addiction is presented. As nimodipine might have anticraving and mood-stabilizing properties and cardio- and neuroprotective properties in the face of cocaine intoxication and might possibly even reverse some cocaine-induced brain deficits, further investigation of the role of nimodipine (and other VSCCBs) in cocaine addiction appears an attractive avenue of future medication development.
近期的临床前研究表明,电压敏感性钙通道阻滞剂(VSCCBs)在治疗可卡因成瘾方面具有应用价值。以下这项双盲安慰剂对照研究,在一家住院药物滥用治疗机构中,对66名近期戒毒的可卡因依赖患者,运用强化的以12步为导向的环境心理社会疗法,研究了VSCCB尼莫地平在减轻可卡因渴求方面的作用。虽然该药物耐受性良好,但在本研究中使用的尼莫地平剂量(每日90毫克)在研究的3周内,在减少背景或线索诱发的可卡因渴求方面并不优于安慰剂。有迹象表明,通过对平稳跟踪眼球运动功能的评估发现,尼莫地平可能会减轻一些可卡因诱发的脑功能缺陷的严重程度。本文提出了评估更高剂量尼莫地平治疗可卡因成瘾的理论依据。由于尼莫地平在面对可卡因中毒时可能具有抗渴求、稳定情绪的特性以及心脏和神经保护特性,甚至可能逆转一些可卡因诱发的脑功能缺陷,进一步研究尼莫地平(以及其他VSCCBs)在可卡因成瘾中的作用似乎是未来药物开发的一个有吸引力的途径。