Yerkes National Primate Research Center, Emory University, 954 Gatewood Road NE, Atlanta, GA 30329, USA.
Psychopharmacology (Berl). 2010 Feb;208(2):191-9. doi: 10.1007/s00213-009-1720-3. Epub 2009 Nov 19.
Acute re-exposure to cocaine or drug cues associated with cocaine use can elicit drug craving and relapse. Neuroimaging studies have begun to define neurobiological substrates underlying the acute effects of cocaine or cocaine cues in cocaine-dependent subjects.
The present study was the first to use functional brain imaging to document acute cocaine-induced changes in brain activity during active drug use in nonhuman primates.
Positron emission tomography imaging with O15-labeled water was used to measure drug-induced changes in cerebral blood flow. The acute effects of cocaine administered noncontingently were characterized in four drug-naïve rhesus monkeys. The same subjects were trained to self-administer cocaine under a fixed ratio schedule during image acquisition. Subsequently, three subjects with an extensive history of cocaine use were trained to self-administer cocaine under a second-order schedule. The same subjects also underwent extinction sessions during which saline was substituted for cocaine under the second-order schedule.
Noncontingent administration of cocaine in drug-naïve subjects induced robust activation of prefrontal cortex localized primarily to the dorsolateral regions. In contrast, the pattern of brain activation induced by self-administered cocaine differed qualitatively and included anterior cingulate cortex. Moreover, drug-associated stimuli during extinction also induced robust activation of prefrontal cortex.
The effects of cocaine and associated cues extend beyond the limbic system to engage brain areas involved in cognitive processes. The identification of neural circuits underlying the direct pharmacological and conditioned stimulus effects of cocaine may be highly relevant toward efforts to develop treatments for cocaine addiction.
急性重新接触可卡因或与可卡因使用相关的药物线索会引起药物渴求并导致复发。神经影像学研究已开始定义可卡因依赖者中可卡因或可卡因线索的急性作用的神经生物学基础。
本研究首次使用功能脑成像技术记录非人类灵长类动物在主动使用药物期间可卡因引起的大脑活动的急性变化。
使用 O15 标记水的正电子发射断层扫描成像来测量脑血流引起的药物变化。在四个药物-naïve 恒河猴中描述了非条件给予可卡因的急性作用。相同的受试者在图像采集期间接受了固定比率方案下的可卡因自我给药训练。随后,三名有大量可卡因使用史的受试者接受了二级方案下的可卡因自我给药训练。相同的受试者还接受了消退课程,在此期间,根据二级方案用盐水代替可卡因。
在药物-naïve 受试者中给予非条件可卡因诱导了前额叶皮层的强烈激活,主要定位于背外侧区域。相比之下,自我给予可卡因引起的大脑激活模式在质量上有所不同,包括前扣带皮层。此外,在消退期间,与药物相关的刺激也会引起前额叶皮层的强烈激活。
可卡因和相关线索的作用不仅限于边缘系统,还涉及参与认知过程的大脑区域。确定可卡因直接药理和条件刺激作用的神经回路可能与开发可卡因成瘾治疗方法的努力高度相关。