Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (45)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Hoogendijk, W. J. G.
Right arrow Articles by Swaab, D. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hoogendijk, W. J. G.
Right arrow Articles by Swaab, D. F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 118, No. 1, 131-143, 1995
© 1995 Oxford University Press


research-article

Image analyser-assisted morphometry of the locus coeruleus in Alzheimer's disease, Parkinson's disease and amyotrophic lateral sclerosis

Witte J. G. Hoogendijk1,3,, Chris W. Pool1, Dirk Troost2, Ed van Zwieten1 and Dick F. Swaab1

1Netherlands Institute for Brain Research Amsterdam, The Netherlands 2Department of Pathology, Academic Medical Centre Amsterdam, The Netherlands 3Valerius Clinic, Free University Amsterdam, The Netherlands

Correspondence to: W. J. G. Hoogendijk, Netherlands Institute for Brain Research, Meibergdreef 33, 1105 AZ Amsterdam, The Netherlands

Several observations suggest that neuronal shrinkage rather than cell death is the major phenomenon in neurodegenerative diseases. In order to make this distinction, smaller cells should also be included in cell counts. Also, morphometric determination of total cell numbers of brain structures is required. Morphometry was performed on the locus coeruleus using a newly developed method to delineate this nucleus from five patients who had died with Alzheimer's disease, five with Parkinson's disease, five with amyotrophic lateral sclerosis and from five control subjects who had died from causes that would not have affected the locus coeruleus. The length and volume of the locus coeruleus and its total number of large pigmented neurons, small unpigmented neurons and glial cells were determined. Since reliable delineation of the boundaries of the locus coeruleus is a requirement for the determination of total cell numbers, an image analyser-assisted procedure was developed. In Alzheimer's disease we found an 82% decrease in the number of large pigmented neurons and a 39% decrease of small unpigmented neurons. In Parkinson's disease, we found a 39% decrease of large pigmented neurons but also a 44% (though not significant) increase of small unpigmented neurons, which is indicative of a shift from large pigmented neurons to small unpigmented neurons in Parkinson's disease. The large pigmented/small unpigmented neuron number ratio was greatly and significantly reduced in Alzheimer's disease, Parkinson's disease and amyotrophic lateral sclerosis. These findings support the hypothesis that the decrease of large pigmented neurons of the locus coeruleus in some neurodegenerative diseases is not entirely due to cell death, but rather to cell shrinkage and a loss of phenotype. This hypothesis may have consequences for the development of therapeutic strategies since atrophied cells can be activated. On the other hand our data confirm that, at least in Alzheimer's disease, large pigmented neurons do also undergo cell death.

image analysis; locus coeruleus; Alzheimer's disease; Parkinson's disease; amyotrophic lateral sclerosis

Received July 11, 1994. Accepted August 30, 1994.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Sci Transl MedHome page
F. K. Wiseman
Cognitive Enhancement Therapy for a Model of Down Syndrome
Science Translational Medicine, November 18, 2009; 1(7): 7ps9 - 7ps9.
[Full Text] [PDF]


Home page
Sci Transl MedHome page
A. Salehi, M. Faizi, D. Colas, J. Valletta, J. Laguna, R. Takimoto-Kimura, A. Kleschevnikov, S. L. Wagner, P. Aisen, M. Shamloo, et al.
Restoration of Norepinephrine-Modulated Contextual Memory in a Mouse Model of Down Syndrome
Science Translational Medicine, November 18, 2009; 1(7): 7ra17 - 7ra17.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
L. Zecca, A. Stroppolo, A. Gatti, D. Tampellini, M. Toscani, M. Gallorini, G. Giaveri, P. Arosio, P. Santambrogio, R. G. Fariello, et al.
The role of iron and copper molecules in the neuronal vulnerability of locus coeruleus and substantia nigra during aging
PNAS, June 29, 2004; 101(26): 9843 - 9848.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
C. Zarow, S. A. Lyness, J. A. Mortimer, and H. C. Chui
Neuronal Loss Is Greater in the Locus Coeruleus Than Nucleus Basalis and Substantia Nigra in Alzheimer and Parkinson Diseases
Arch Neurol, March 1, 2003; 60(3): 337 - 341.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
M. Simonetta Moreau, S. Meunier, M. Vidailhet, S. Pol, M. Galitzky, and O. Rascol
Transmission of group II heteronymous pathways is enhanced in rigid lower limb of de novo patients with Parkinson's disease
Brain, September 1, 2002; 125(9): 2125 - 2133.
[Abstract] [Full Text] [PDF]


Home page
Arch Gen PsychiatryHome page
W. J. G. Hoogendijk, I. E. C. Sommer, C. W. Pool, W. Kamphorst, M. A. Hofman, P. Eikelenboom, and D. F. Swaab
Lack of Association Between Depression and Loss of Neurons in the Locus Coeruleus in Alzheimer Disease
Arch Gen Psychiatry, January 1, 1999; 56(1): 45 - 51.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.