Nerve cell loss in the thalamic mediodorsal nucleus in Huntington's disease

Citation
H. Heinsen et al., Nerve cell loss in the thalamic mediodorsal nucleus in Huntington's disease, ACT NEUROP, 97(6), 1999, pp. 613-622
Citations number
118
Categorie Soggetti
Neurosciences & Behavoir
Journal title
ACTA NEUROPATHOLOGICA
ISSN journal
00016322 → ACNP
Volume
97
Issue
6
Year of publication
1999
Pages
613 - 622
Database
ISI
SICI code
0001-6322(199906)97:6<613:NCLITT>2.0.ZU;2-J
Abstract
We estimated the total neurone number, glial number, and glial index (ratio glial cells/neurone) in the thalamic mediodorsal nucleus (MD) in seven pat ients suffering from Huntington's disease (HD; four males, three females, m ean age 52.4 +/- 13.6 years) and age- and sex-matched controls (four males, three females, mean age 53.6 +/- 12.1 years) by means of a stereological p rotocol. The mean total neurone number (N-(T) over bar) in the MD of contro ls was 2,985,188 +/- 174,710, the mean glial number (G-T; astrocytes, oligo dendrocytes) 21,785,008 +/- 2,986,678, and the glial index 7.29 +/- 0.88. I n HD, the average neurone number was decreased by 23.8% to 2,275,321 +/- 24 7,162 (Mann-Whitney U-test P < 0.05), the mean glial number by 29.7 % to 15 ,318,895 +/- 1,722,524 (Mann-Whitney U-test P < 0.05), the glial index was slightly reduced to 6.81 +/- 1.06. Gallyas' impregnation for the demonstrat ion of fibrous astroglia gave strongly positive results in all cases with H D and negative results in the controls. The morpho-functional correlation o f the results is complicated because individual variability, presence of se gregated and parallel neuronal circuits, and plasticity of the adult human CNS must be considered.