Department of Neurosurgery, Farber Institute for Neurosciences, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
J Neurosci Res. 2009 Dec;87(16):3671-8. doi: 10.1002/jnr.22158.
We previously reported that administration of the synthetic cannabinoid agonist WIN 55,212-2 causes an increase in norepinephrine (NE) efflux in the frontal cortex (FC). The present study examined the expression levels of alpha2- and beta1-adrenergic receptors (ARs) as well as the norepinephrine transporter (NET) in the FC of rats following exposure to WIN 55,212-2. Rats received systemic injection of WIN 55,212-2 (3 mg/kg) acutely or for 7 days. Another group of rats received repeated WIN 55,212-2 treatment followed by a period of abstinence. Control rats received vehicle injections. Rats were euthanized 30 min after the last WIN 55,212-2 injection, the FC was microdissected, and protein extracts were probed for alpha2-AR, beta1-AR, and NET. Results showed that beta1-AR expression was significantly decreased following repeated WIN 55,212-2 treatment but significantly increased following a period of abstinence. alpha2-AR expression showed no significant change in all groups examined. NET expression was significantly decreased following acute WIN 55,212-2 treatment, with no changes following chronic administration or a period of abstinence. Alterations in NET may arise from modulation of cannabinoid receptors (CB1) that are localized to noradrenergic axon terminals as we demonstrate colocalization of CB1 receptor and NET in the same cortical axonal processes. The present findings support significant alterations in adrenergic receptor and NET expression in the FC after WIN 55,212 exposure that may underlie the reported changes in attention, cognition, and anxiety commonly observed after cannabinoid exposure.
我们之前曾报道过,合成大麻素激动剂 WIN 55,212-2 的给药会导致前额皮质(FC)中去甲肾上腺素(NE)外排增加。本研究检测了 WIN 55,212-2 暴露后大鼠 FC 中 alpha2-和 beta1-肾上腺素能受体(AR)以及去甲肾上腺素转运体(NET)的表达水平。大鼠接受全身注射 WIN 55,212-2(3mg/kg),急性或连续 7 天。另一组大鼠接受重复 WIN 55,212-2 治疗,然后进行一段时间的戒断。对照组大鼠接受载体注射。大鼠在最后一次 WIN 55,212-2 注射后 30 分钟被安乐死,FC 被微分离,蛋白质提取物用于探测 alpha2-AR、beta1-AR 和 NET。结果表明,反复 WIN 55,212-2 处理后 beta1-AR 表达显著降低,但戒断后明显增加。所有检测的组 alpha2-AR 表达均无明显变化。NET 表达在急性 WIN 55,212-2 处理后显著降低,慢性给药或戒断后无变化。NET 的变化可能源于位于去甲肾上腺素能轴突末端的大麻素受体(CB1)的调制,正如我们在同一皮质轴突过程中显示 CB1 受体和 NET 的共定位所证明的那样。本研究结果支持 WIN 55,212 暴露后 FC 中肾上腺素能受体和 NET 表达的显著改变,这可能是大麻素暴露后常见的注意力、认知和焦虑变化的基础。