Institute of Clinical Neuroanatomy, Neuroscience Center, Goethe-University, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.
Brain. 2011 Jan;134(Pt 1):24-35. doi: 10.1093/brain/awq327. Epub 2010 Nov 28.
The pre-Bötzinger complex has been identified as an essential part of the medullary respiratory network in mammals. Although well described in experimental animals, its localization in the human brain has remained elusive. Using serially sectioned brainstems from 19 normal individuals and patients suffering from neurodegenerative diseases (multiple system atrophy, n = 10; spinocerebellar ataxia type 3, n = 8), we have identified a circumscribed area of the ventrolateral medulla that represents the human homologue of the pre-Bötzinger complex and have mapped its longitudinal and horizontal extents. The presumed human pre-Bötzinger complex is characterized by an aggregation of loosely scattered, small and lipofuscin-rich neurons, which contain neurokinin 1 receptor as well as somatostatin, but are negative for markers of monoaminergic neurons and of motoneurons. In brains of patients suffering from multiple systems atrophy (with central respiratory deficits but without swallowing problems), pre-Bötzinger complex neurons were reduced, whereas pharyngeal motoneurons of the ambigual nucleus were not affected. In contrast, in brains of patients with spinocerebellar ataxia 3 (no reported central respiratory deficits but with dysphagia), pre-Bötzinger complex neurons were preserved, whereas ambigual motoneurons, which control swallowing, were diminished. These pathoanatomical findings support the view, that affection of the central respiratory network, including the pre-Bötzinger complex, contributes to breathing disorders in multiple system atrophy, whereas damage to ambigual motoneurons is important for pathogenesis of breathing disturbances and dysphagia in patients with spinocerebellar ataxia type 3. On the basis of these findings, the putative human homologue of the pre-Bötzinger complex can now be reliably delineated on pigment-Nissl-stained sections, making neuropathological investigations of central respiratory disturbances feasible.
已确定 Pre-Bötzinger 复合体是哺乳动物髓质呼吸网络的重要组成部分。虽然在实验动物中得到了很好的描述,但它在人脑中的定位仍然难以捉摸。我们使用来自 19 名正常个体和患有神经退行性疾病(多系统萎缩症,n = 10;脊髓小脑共济失调 3 型,n = 8)的连续切片脑干,确定了延髓腹外侧的一个限定区域,该区域代表人类 Pre-Bötzinger 复合体的同源物,并绘制了其纵向和横向范围。假定的人类 Pre-Bötzinger 复合体的特征是聚集了松散分散的、小的和脂褐素丰富的神经元,这些神经元包含神经激肽 1 受体以及生长抑素,但对单胺能神经元和运动神经元的标志物呈阴性。在患有多系统萎缩症(中枢性呼吸缺陷但无吞咽问题)的患者大脑中,Pre-Bötzinger 复合体神经元减少,而疑核的咽运动神经元不受影响。相比之下,在患有脊髓小脑共济失调 3 型的患者大脑中(无报道的中枢性呼吸缺陷但有吞咽困难),Pre-Bötzinger 复合体神经元得以保留,而控制吞咽的疑核运动神经元则减少。这些病理解剖学发现支持这样的观点,即中枢呼吸网络的受累,包括 Pre-Bötzinger 复合体,导致多系统萎缩症的呼吸障碍,而疑核运动神经元的损伤对于脊髓小脑共济失调 3 型患者呼吸紊乱和吞咽困难的发病机制很重要。基于这些发现,现在可以在色素尼氏染色切片上可靠地描绘假定的人类 Pre-Bötzinger 复合体同源物,从而使中枢呼吸紊乱的神经病理学研究成为可能。