Neuropathology Unit, Division of Brain Sciences, Department of Medicine, Imperial College London, London, UK.
Department of Eye Pathology, Institute of Ophthalmology, University College London, London, UK.
Neuropathol Appl Neurobiol. 2018 Dec;44(7):647-662. doi: 10.1111/nan.12513. Epub 2018 Aug 13.
Although the nucleus of the vertical limb of the diagonal band of Broca (nvlDBB) is the second largest cholinergic nucleus in the basal forebrain, after the nucleus basalis of Meynert, it has not generally been a focus for studies of neurodegenerative disorders. However, the nvlDBB has an important projection to the hippocampus and discrete lesions of the rostral basal forebrain have been shown to disrupt retrieval memory function, a major deficit seen in patients with Lewy body disorders. One reason for its neglect is that the anatomical boundaries of the nvlDBB are ill defined and this area of the brain is not part of routine diagnostic sampling protocols. We have reviewed the history and anatomy of the nvlDBB and now propose guidelines for distinguishing nvlDBB from other neighbouring cholinergic cell groups for standardizing future clinicopathological work. Thorough review of the literature regarding neurodegenerative conditions reveals inconsistent results in terms of cholinergic neuronal loss within the nvlDBB. This is likely to be due to the use of variable neuronal inclusion criteria and omission of cholinergic immunohistochemical markers. Extrapolating from those studies showing a significant nvlDBB neuronal loss in Lewy body dementia, we propose an anatomical and functional connection between the cholinergic component of the nvlDBB (Ch2) and the CA2 subfield in the hippocampus which may be especially vulnerable in Lewy body disorders.
虽然 Broca 垂直束的核(nvlDBB)是基底前脑第二大胆碱能核,但仅次于基底核 Meynert,它通常不是神经退行性疾病研究的焦点。然而,nvlDBB 对海马有重要的投射,并且已经证明,前基底前脑的离散性损伤会破坏检索记忆功能,这是路易体障碍患者的主要缺陷之一。其被忽视的一个原因是 nvlDBB 的解剖边界不明确,而且大脑的这个区域不在常规诊断采样方案中。我们已经回顾了 nvlDBB 的历史和解剖结构,现在提出了区分 nvlDBB 与其他邻近胆碱能细胞群的指南,以标准化未来的临床病理工作。对神经退行性疾病相关文献的全面回顾显示,nvlDBB 内胆碱能神经元丢失的结果不一致。这可能是由于使用了可变的神经元纳入标准,以及省略了胆碱能免疫组织化学标志物。从那些显示路易体痴呆中 nvlDBB 神经元大量丢失的研究中推断,我们提出了 nvlDBB 的胆碱能成分(Ch2)与海马 CA2 亚区之间的解剖和功能联系,这在路易体障碍中可能特别脆弱。