Norris Christopher, Loureiro Michael, Kramar Cecilia, Zunder Jordan, Renard Justine, Rushlow Walter, Laviolette Steven R
Addiction Research Group, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.
Department of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.
Neuropsychopharmacology. 2016 Nov;41(12):2839-2850. doi: 10.1038/npp.2016.93. Epub 2016 Jun 14.
Emerging evidence suggests that the largest phytochemical component of cannabis, cannabidiol (CBD), may possess pharmacotherapeutic properties in the treatment of neuropsychiatric disorders. CBD has been reported to functionally interact with both the mesolimbic dopamine (DA) and serotonergic (5-HT) receptor systems. However, the underlying mechanisms by which CBD may modulate emotional processing are not currently understood. Using a combination of in vivo electrophysiological recording and fear conditioning in rats, the present study aimed to characterize the behavioral, neuroanatomical, and pharmacological effects of CBD within the mesolimbic pathway, and its possible functional interactions with 5-HT and DAergic transmission. Using targeted microinfusions of CBD into the shell region of the mesolimbic nucleus accumbens (NASh), we report that intra-NASh CBD potently blocks the formation of conditioned freezing behaviors. These effects were challenged with DAergic, cannabinoid CB1 receptor, and serotonergic (5-HT) transmission blockade, but only 5-HT blockade restored associative conditioned freezing behaviors. In vivo intra-ventral tegmental area (VTA) electrophysiological recordings revealed that behaviorally effective doses of intra-NASh CBD elicited a predominant decrease in spontaneous DAergic neuronal frequency and bursting activity. These neuronal effects were reversed by simultaneous blockade of 5-HT receptor transmission. Finally, using a functional contralateral disconnection procedure, we demonstrated that the ability of intra-NASh CBD to block the formation of conditioned freezing behaviors was dependent on intra-VTA GABAergic transmission substrates. Our findings demonstrate a novel NAcVTA circuit responsible for the behavioral and neuronal effects of CBD within the mesolimbic system via functional interactions with serotonergic 5-HT receptor signaling.
新出现的证据表明,大麻中最大的植物化学成分大麻二酚(CBD)可能在治疗神经精神疾病方面具有药物治疗特性。据报道,CBD在功能上与中脑边缘多巴胺(DA)和5-羟色胺能(5-HT)受体系统相互作用。然而,目前尚不清楚CBD调节情绪加工的潜在机制。本研究结合大鼠体内电生理记录和恐惧条件反射,旨在表征中脑边缘通路中CBD的行为、神经解剖学和药理学作用,以及其与5-HT和多巴胺能传递可能的功能相互作用。通过将CBD靶向微量注射到中脑边缘伏隔核壳区(NASh),我们发现NASh内注射CBD可有效阻断条件性僵住行为的形成。这些作用受到多巴胺能、大麻素CB1受体和5-羟色胺能(5-HT)传递阻断的挑战,但只有5-HT阻断可恢复联想性条件性僵住行为。体内腹侧被盖区(VTA)电生理记录显示,行为有效剂量的NASh内注射CBD可使自发多巴胺能神经元频率和爆发活动显著降低。同时阻断5-HT受体传递可逆转这些神经元效应。最后,使用功能性对侧切断程序,我们证明NASh内注射CBD阻断条件性僵住行为形成的能力依赖于VTA内的GABA能传递底物。我们的研究结果表明,通过与5-羟色胺能5-HT受体信号的功能相互作用,一种新的伏隔核-腹侧被盖区回路负责中脑边缘系统中CBD的行为和神经元效应。