Soderstrom Ken, Tian Qiyu
Department of Pharmacology and Toxicology, Brody School of Medicine, East Carolina University, Greenville, NC 27834, USA.
Psychopharmacology (Berl). 2008 Aug;199(2):265-73. doi: 10.1007/s00213-008-1190-z. Epub 2008 May 29.
CB(1) cannabinoid receptors are distinctly expressed at high density within several regions of zebra finch telencephalon, including those known to be involved in song learning (lMAN and Area X) and production (HVC and RA) because (1) exposure to cannabinoid agonists during developmental periods of auditory and sensory-motor song learning alters song patterns produced later in adulthood and (2) densities of song region expression of CB(1) waxes and wanes during song learning. It is becoming clear that CB(1)-receptor-mediated signaling is important to normal processes of vocal development.
To better understand the mechanisms involved in cannabinoid modulation of vocal behavior, we have investigated the dose-response relationship between systemic cannabinoid exposure and changes in neuronal activity (as indicated by expression of the transcription factor, c-Fos) within telencephalic brain regions, with established involvement in song learning and/or control.
In adults, we have found that low doses (0.1 mg/kg) of the cannabinoid agonist WIN-55212-2 decrease neuronal activity (as indicated by densities of c-fos-expressing nuclei) within vocal motor regions of caudal telencephalon (HVC and RA) while higher doses (3 mg/kg) stimulate activity. Both effects were reversed by pretreatment with the CB(1)-selective antagonist rimonabant. Interestingly, no effects of cannabinoid treatment were observed within the rostral song regions lMAN and Area X, despite distinct and dense CB(1) receptor expression within these areas.
Overall, our results demonstrate that, depending on dosage, CB(1) agonism can both inhibit and stimulate neuronal activity within brain regions controlling adult vocal motor output, implicating involvement of multiple CB(1)-sensitive neuronal circuits.
CB(1)大麻素受体在斑胸草雀端脑的几个区域中以高密度特异性表达,包括那些已知参与鸣叫学习的区域(lMAN和X区)以及鸣叫产生的区域(HVC和RA),原因如下:(1)在听觉和感觉运动鸣叫学习的发育阶段接触大麻素激动剂会改变成年后期产生的鸣叫模式;(2)在鸣叫学习过程中,CB(1)在鸣叫区域的表达密度会有起伏。越来越清楚的是,CB(1)受体介导的信号传导对正常的发声发育过程很重要。
为了更好地理解大麻素对发声行为调节的机制,我们研究了全身大麻素暴露与端脑区域神经元活动变化(由转录因子c-Fos的表达表示)之间的剂量反应关系,这些区域已确定参与鸣叫学习和/或控制。
在成年鸟中,我们发现低剂量(0.1mg/kg)的大麻素激动剂WIN-55212-2会降低尾端脑发声运动区域(HVC和RA)的神经元活动(由表达c-fos的细胞核密度表示),而高剂量(3mg/kg)则会刺激活动。两种效应都被CB(1)选择性拮抗剂利莫那班预处理所逆转。有趣的是,尽管在喙端鸣叫区域lMAN和X区有明显且密集的CB(1)受体表达,但未观察到大麻素处理对这些区域有影响。
总体而言,我们的结果表明,根据剂量不同,CB(1)激动作用既能抑制也能刺激控制成年发声运动输出的脑区中的神经元活动,这表明多个CB(1)敏感神经元回路参与其中。