Meng Wei, Wang Songhua, Yao Lihua, Zhang Nan, Li Dongfeng
Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal UniversityNanchang, China; School of Life Science, South China Normal UniversityGuangzhou, China.
School of Life Science, Jiangxi Science and Technology Normal University Nanchang, China.
Front Cell Neurosci. 2017 Feb 28;11:51. doi: 10.3389/fncel.2017.00051. eCollection 2017.
Songbirds are a useful model for the study of learned vocal behavior in vertebrates. The robust nucleus of the arcopallium (RA) is a premotor nucleus in the vocal motor pathway. It receives excitatory synaptic inputs from the anterior forebrain pathway. RA also receives cholinergic inputs from the ventral paleostriatum of the basal forebrain. Our previous study showed that carbachol, a non-selective cholinergic receptor agonist, modulates the electrophysiology of RA projection neurons (PNs), indicating that cholinergic modulation of RA may play an important role in song production. However, the receptor mechanisms underlying these effects are poorly understood. In the present study, we investigated the electrophysiological properties of two acetylcholine receptors on the RA PNs of adult male zebra finches using whole-cell current clamp. Our results demonstrate that activation of muscarinic acetylcholine receptors (mAChRs) simulate the effects of carbachol. Both carbachol and the mAChR agonist muscarine produced a decrease in the excitability of RA PNs and a hyperpolarization of the membrane potential. The mAChR antagonist atropine blocked the effects of carbachol. Activation of nicotinic acetylcholine receptors (nAChRs) with nAChR agonist nicotine or DMPP had no effect on the excitability of RA PNs, and the nAChR antagonist mecamylamine failed to inhibit the effects of carbachol. These results suggest that mAChRs, but not nAChRs, primarily modulate the effects of carbachol on the activity of RA PNs. Collectively, these findings contribute to our understanding of the mechanism of cholinergic modulation in the vocal nuclei of songbirds.
鸣禽是研究脊椎动物习得性发声行为的有用模型。古纹状体粗核(RA)是发声运动通路中的一个运动前核。它从前脑通路接收兴奋性突触输入。RA还从基底前脑的腹侧古纹状体接收胆碱能输入。我们之前的研究表明,卡巴胆碱,一种非选择性胆碱能受体激动剂,可调节RA投射神经元(PNs)的电生理,表明RA的胆碱能调节可能在鸣叫产生中起重要作用。然而,这些作用背后的受体机制尚不清楚。在本研究中,我们使用全细胞电流钳研究了成年雄性斑胸草雀RA PNs上两种乙酰胆碱受体的电生理特性。我们的结果表明,毒蕈碱型乙酰胆碱受体(mAChRs)的激活模拟了卡巴胆碱的作用。卡巴胆碱和mAChR激动剂毒蕈碱均使RA PNs的兴奋性降低,膜电位超极化。mAChR拮抗剂阿托品阻断了卡巴胆碱的作用。用nAChR激动剂尼古丁或DMPP激活烟碱型乙酰胆碱受体(nAChRs)对RA PNs的兴奋性没有影响,nAChR拮抗剂美加明也未能抑制卡巴胆碱的作用。这些结果表明,主要是mAChRs而非nAChRs调节卡巴胆碱对RA PNs活性的影响。总的来说,这些发现有助于我们理解鸣禽发声核团中胆碱能调制机制。