Jürgens U
German Primate Centre, Göttingen.
Behav Brain Res. 1994 Jun 30;62(2):107-17. doi: 10.1016/0166-4328(94)90017-5.
This is a review of our current knowledge about the role of the periaqueductal grey (PAG) in vocal control. It shows that electrical stimulation of the PAG can evoke species-specific calls with short latency and low habituation in many mammals. The vocalization-eliciting region contains neurones the activity of which is correlated with the activity of specific laryngeal muscles. Lesioning studies show that destruction of the PAG and laterally bordering tegmentum can cause mutism without akinesia. Neuroanatomical studies reveal that the PAG lacks direct connections with the majority of phonatory motoneurone pools but is connected with the periambigual reticular formation, an area which does have direct connections with all phonatory motor nuclei. The PAG receives a glutamatergic input from several sensory areas, such as the superior and inferior colliculi, solitary tract nucleus and spinal trigeminal nucleus. Glutamatergic input, in addition, reaches it from numerous limbic structures the stimulation of which also produces vocalization, such as the anterior cingulate cortex, septum, amygdala, hypothalamus and midline thalamus. Pharmacological blocking of this glutamatergic input causes mutism. The glutamatceptive vocalization-controlling neurones are under a tonic inhibitory control from GABAergic neurones. Removal of this inhibitory input lowers the threshold for the elicitation of vocalization by external stimuli. A modulatory control on vocalization threshold is also exerted by glycinergic, opioidergic, cholinergic, histaminergic and, possibly, noradrenergic and dopaminergic afferents. It is proposed that the PAG serves as a link between sensory and motivation-controlling structures on the one hand and the periambigual reticular formation coordinating the activity of the different phonatory muscles on the other.
这是一篇关于中脑导水管周围灰质(PAG)在发声控制中作用的当前知识综述。研究表明,在许多哺乳动物中,电刺激PAG可在短潜伏期内引发物种特异性叫声,且不易产生习惯化。引发发声的区域包含一些神经元,其活动与特定喉肌的活动相关。损伤研究表明,破坏PAG及其外侧相邻的被盖可导致缄默但无运动不能。神经解剖学研究显示,PAG与大多数发声运动神经元池缺乏直接联系,但与疑核周围网状结构相连,该区域确实与所有发声运动核有直接联系。PAG从几个感觉区域接收谷氨酸能输入,如上下丘、孤束核和三叉神经脊束核。此外,谷氨酸能输入还来自众多边缘结构,刺激这些结构也会产生发声,如前扣带回皮质、隔区、杏仁核、下丘脑和中线丘脑。对这种谷氨酸能输入进行药理学阻断会导致缄默。感受谷氨酸的发声控制神经元受到来自γ-氨基丁酸能神经元的紧张性抑制控制。去除这种抑制性输入会降低外部刺激引发发声的阈值。甘氨酸能、阿片样物质能、胆碱能、组胺能以及可能的去甲肾上腺素能和多巴胺能传入纤维也对发声阈值施加调节控制。有人提出,PAG一方面作为感觉和动机控制结构之间的联系,另一方面作为协调不同发声肌肉活动的疑核周围网状结构之间的联系。