Treweek Jennifer B, Sun Chengzao, Mayorov Alexander V, Qi Longwu, Levy Coree L, Roberts Amanda J, Dickerson Tobin J, Janda Kim D
Department of Chemistry, The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
J Med Chem. 2008 Nov 13;51(21):6866-75. doi: 10.1021/jm800506v. Epub 2008 Oct 16.
One approach to treating drug abuse uses antidrug antibodies to immunize subjects against the illicit substance rather than administering therapeutics that target the specific CNS site of action. At present, passive vaccination has recognized efficacy in treating certain gross symptoms of drug misuse, namely, motor activation, self-administration, and overdose. However, the potential for antibodies to prevent drug-induced changes involving finer cognitive processes, such as benzodiazepine-associated amnesia, remains unexplored. To address this concept, a flunitrazepam hapten was synthesized and employed in the generation of a panel of high affinity monoclonal antibodies. Anti-flunitrazepam mAb RCA3A3 ( K d,app = 200 nM) was tested in a mouse model of passive immunization and subsequent mole-equivalent challenge with flunitrazepam. Not only was flunitrazepam-induced sedation prevented but immunization also conferred protection to memory consolidation as assessed through contextual and cued fear conditioning paradigms. These results provide evidence that immunopharmacotherapeutic blockade of drug intoxication also preserves complex cognitive function.
一种治疗药物滥用的方法是使用抗药物抗体对受试者进行免疫,使其对非法药物产生抵抗力,而不是给予针对特定中枢神经系统作用位点的治疗药物。目前,被动免疫接种在治疗药物滥用的某些明显症状方面已被证实有效,即运动激活、自我给药和过量用药。然而,抗体预防涉及更精细认知过程的药物诱导变化的潜力,如与苯二氮䓬相关的失忆,仍未得到探索。为了验证这一概念,合成了一种氟硝西泮半抗原,并用于生成一组高亲和力单克隆抗体。抗氟硝西泮单克隆抗体RCA3A3(Kd,app = 200 nM)在被动免疫小鼠模型中进行了测试,并随后用氟硝西泮进行了摩尔当量攻击。结果显示,氟硝西泮诱导的镇静作用不仅得到了预防,而且通过情境和线索恐惧条件反射范式评估,免疫接种还对记忆巩固起到了保护作用。这些结果证明,药物中毒的免疫药物治疗性阻断也能保留复杂的认知功能。