Dendritic reorganisation in the basal forebrain under degenerative conditions and its defects in Alzheimer's disease. III. The basal forebrain compared with other subcortical areas
- 9 January 1995
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 351 (2) , 223-246
- https://doi.org/10.1002/cne.903510204
Abstract
The distribution of the reticular neuronal type in the human brain and its involvement in both degeneration and dendritic reorganisation under the conditions of ageing, Korsakoff's disease (KD), Alzheimer's disease (AD), and Parkinson's disease (PD) was comparatively investigated after Golgi impregnation. Reticular neurones are distributed throughout different areas along the brain axis. The cholinergic basal forebrain nuclei, i.e., the basal nucleus of Meynert, the nucleus of the diagonal band, and the medial septal nucleus form the most rostral part of this network of “open nuclei,” which is collectively referred to as the “reticular core.” Reticular neurones of the following areas were quantitatively investigated by a computer‐based three‐dimensional analysis: caudate nucleus, globus pallidus, medial septal nucleus, nucleus of the vertical limb of the diagonal band, basal nucleus, medial amygdaloid nucleus, reticular thalamic nucleus, lateral hypothalamic area, subthalamic nucleus, substantia nigra, locus coeruleus, pedunculopontine tegmental nucleus, and raphe magnus nucleus. There are three major findings. First, neurones that were found to be susceptible to degeneration in AD were largely part of the same neuronal populations prone to degeneration during ageing, in KD and PD. Thus, areas could be classified according to their overall degree of vulnerability under the present degenerative conditions as being highly vulnerable (basal forebrain nuclei, caudate nucleus, locus coeruleus), moderately vulnerable (medial amygdaloid nucleus, raphe magnus nucleus, lateral hypothalamic area, substantia nigra, pedunculopontine tegmental nucleus), or marginally vulnerable (globus pallidus, subthalamic nucleus, reticular thalamic nucleus). Second, neuronal populations that are particularly vulnerable to degenerative changes show a high degree of structural plasticity. Third, the degree of this dendritic plasticity is inversely related to the complexity of dendritic arborisation of the neurone. It is concluded that the sparsely ramified reticular type of neurone forms a pool of pluripotent neurones that have retained their plastic capacity throughout life, which makes them vulnerable to a variety of perturbations. © 1995 Willy‐Liss, Inc.Keywords
This publication has 98 references indexed in Scilit:
- Tau protein and the neurofibrillary pathology of Alzheimer's diseaseTrends in Neurosciences, 1993
- Clinico-pathological correlations in Parkinson's diseaseClinical Neurology and Neurosurgery, 1992
- AGEING AND PARKINSON'S DISEASE: SUBSTANTIA NIGRA REGIONAL SELECTIVITYBrain, 1991
- Amyloid beta protein precursor is a mitogenBiochemical and Biophysical Research Communications, 1989
- The basal nucleus of Meynert revised: the nerve cell number decreases with ageArchives of Gerontology and Geriatrics, 1989
- The pontomesencephalotegmental cholinergic system does not degenerate in Alzheimer's diseaseNeuroscience Letters, 1989
- Hypothalamic pathology in Alzheimer's diseaseNeuroscience Letters, 1987
- Absolute number of neurons and thickness of the cerebral cortex during aging, senile and vascular dementia, and Pick's and Alzheimer's diseasesNeuroscience and Behavioral Physiology, 1973
- ParkinsonismNeurology, 1967
- Zur Klinik und Pathologie der Alzheimerschen KrankheitArchiv Fur Psychiatrie Und Nervenkrankheiten, 1928