Brain Imaging Center, McLean Hospital, Harvard Medical School, 115 Mill, St. Belmont, MA 02478, USA.
Psychopharmacology (Berl). 2011 Oct;217(3):367-75. doi: 10.1007/s00213-011-2292-6. Epub 2011 Apr 15.
Chronic cocaine exposure has been associated with progressive brain structural and functional changes. Clarifying mechanisms underlying cocaine's progressive brain effects may help in the development of effective cocaine abuse treatments.
We used a controlled squirrel monkey model of chronic cocaine exposure (45 mg/kg/week for 9 months) combined with ultra-high magnetic field (9.4 T) proton magnetic resonance spectroscopy to prospectively measure putamen metabolite changes.
Proton metabolites were measured with a STEAM sequence, quantified with LCModel using a simulated basis set, and expressed as metabolite/total creatine (tCr) ratios.
We found cocaine-induced time-dependent changes in putamen glutamate/tCr and glutamine/tCr metabolite ratios suggestive of altered glutamate compartmentalization, neurotransmission, and metabolism. By contrast, saline-treated monkeys exhibited no metabolite changes over time. The time course of cocaine-induced metabolite abnormalities we detected is consistent with the apparent time course of glutamate abnormalities identified in a cross-sectional study in human cocaine users, as well as with microdialysis findings in rodent models of repeated cocaine exposure.
Together, these findings suggests that this squirrel monkey model may be useful for characterizing glutamatergic changes associated with cocaine exposure and for determining efficacies of treatments designed to mitigate cocaine-induced glutamatergic system dysfunction.
慢性可卡因暴露与大脑结构和功能的进行性变化有关。阐明可卡因进行性脑效应的机制可能有助于开发有效的可卡因滥用治疗方法。
我们使用慢性可卡因暴露的受控松鼠猴模型(9 个月内每周 45mg/kg)结合超高磁场(9.4T)质子磁共振波谱,前瞻性测量壳核代谢物变化。
使用 STEAM 序列测量质子代谢物,使用 LCModel 使用模拟基组进行定量,并表示为代谢物/总肌酸(tCr)比值。
我们发现可卡因诱导的壳核谷氨酸/tCr 和谷氨酰胺/tCr 代谢物比值的时间依赖性变化提示谷氨酸区室化、神经传递和代谢改变。相比之下,盐水处理的猴子在整个研究过程中没有代谢物变化。我们检测到的可卡因诱导的代谢物异常的时间过程与人类可卡因使用者的横断面研究中确定的谷氨酸异常的明显时间过程以及重复可卡因暴露的啮齿动物模型中的微透析发现一致。
这些发现表明,这种松鼠猴模型可能有助于表征与可卡因暴露相关的谷氨酸能变化,并确定旨在减轻可卡因诱导的谷氨酸能系统功能障碍的治疗方法的疗效。