Hippocampal neuronal loss in the CA1 and CA3 areas of Alzheimer's disease patients.

BACKGROUND It is believed that in Alzheimer's disease (AD) some areas of the brain are particularly vulnerable to specific degenerative processes and that they could exhibit neuronal dysfunction in the earliest stage of the disease. The implications of the hippocampus in memory processes are very well known and it is likely that the hippocampus would be among the first areas of the brain affected by the pathogenic mechanisms occurring in AD. However, the distinction between the neurodegenerative changes that accompany normal ageing and those that characterize AD is not clear. Also, the distribution of the hippocampal cell loss in both normal aging and AD is not very well understood. SUBJECTS AND METHODS In this context, we focused on the quantification of the neuronal density in the four specific areas of the hippocampus (CA1-CA4) of AD brains, as compared to an age-matched control group, by using the Nissl staining technique. RESULTS We found a significant reduction of neuronal density especially in the CA1 and CA3 hippocampal areas. The most prominent decrease was found at the CA1 area level, as compared to all other 3 areas which were analyzed. CONCLUSIONS In the present study we managed to demonstrate and confirm a significant neuronal loss of hippocampus in AD, as compared to an age-matched control group. Moreover, it seems that this decrease of hippocampal neuronal density is more prominent especially at the CA1 and also in the CA3 hippocampal areas. This could have important implications in the design of therapeutic and investigative strategies of AD. However, larger samples are necessary in order to provide the basis for firmer conclusions in this area of research.

[1]  B. Pakkenberg,et al.  No evidence for loss of hippocampal neurons in non‐Alzheimer dementia patients , 2004, Acta neurologica Scandinavica.

[2]  Michael W. Weiner,et al.  Selective Disruption of the Cerebral Neocortex in Alzheimer's Disease , 2010, PloS one.

[3]  Timothy A. Pedley,et al.  Epilepsy : a comprehensive textbook , 2008 .

[4]  A. Ciobica,et al.  Aspects Regarding the Neurobiology of Psycho-Affective Functions , 2012 .

[5]  Stavros J. Baloyannis,et al.  Mitochondrial alterations in Alzheimer's disease. , 2006, Journal of Alzheimer's disease : JAD.

[6]  S. Pavarini,et al.  [Alzheimer's disease influence on the perception of quality of life from the elderly people]. , 2010, Revista da Escola de Enfermagem da U S P.

[7]  Alin Ciobica,et al.  Changes of some oxidative stress markers in the serum of patients with mild cognitive impairment and Alzheimer's disease , 2010, Neuroscience Letters.

[8]  A. Hannan,et al.  The Latent Stem Cell Population Is Retained in the Hippocampus of Transgenic Huntington's Disease Mice but Not Wild-Type Mice , 2011, PloS one.

[9]  Z. Khachaturian Diagnosis of Alzheimer's disease. , 1985, Archives of neurology.

[10]  E. Mufson,et al.  Effect of neocortical and hippocampal amyloid deposition upon galaninergic and cholinergic neurites in AβPPswe/PS1ΔE9 mice. , 2011, Journal of Alzheimer's disease : JAD.

[11]  K. Valente,et al.  Increased PLA2 activity in the hippocampus of patients with temporal lobe epilepsy and psychosis. , 2011, Journal of psychiatric research.

[12]  Huaxi Xu,et al.  APP processing in Alzheimer's disease , 2011, Molecular Brain.

[13]  S. Khanna,et al.  Patterns of hippocampal neuronal loss and axon reorganization of the dentate gyrus in the mouse pilocarpine model of temporal lobe epilepsy , 2009, Journal of neuroscience research.

[14]  B. Hyman,et al.  Region-specific dissociation of neuronal loss and neurofibrillary pathology in a mouse model of tauopathy. , 2006, The American journal of pathology.

[15]  Stavros J. Baloyannis,et al.  Morphological Changes of the Human Purkinje Cells and Deposition of Neuritic Plaques and Neurofibrillary Tangles on the Cerebellar Cortex of Alzheimer’s Disease , 2010, American journal of Alzheimer's disease and other dementias.

[16]  A. Ciobica,et al.  Cardiovascular risk factors as potential markers for mild cognitive impairment and Alzheimer's disease. , 2011, Psychiatria Danubina.

[17]  J. Troncoso,et al.  Differences in the pattern of hippocampal neuronal loss in normal ageing and Alzheimer's disease , 1994, The Lancet.

[18]  G. Juckel,et al.  Are routine methods good enough to stain senile plaques and neurofibrillary tangles in different brain regions of demented patients? , 2011, Psychiatria Danubina.

[19]  G. Šimić,et al.  Volume and number of neurons of the human hippocampal formation in normal aging and Alzheimer's disease , 1997, The Journal of comparative neurology.

[20]  Luana Flávia da Silva Talmelli,et al.  [Functional independence level and cognitive deficit in elderly individuals with Alzheimer's disease]. , 2010, Revista da Escola de Enfermagem da U S P.

[21]  H G Wieser,et al.  Human hippocampus associates information in memory. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[22]  W. M. van der Flier,et al.  Hippocampal atrophy in Alzheimer disease: Age matters , 2006, Neurology.

[23]  Y. Suh,et al.  Apoptosis in subicular neurons: A comparison between suicide and Addison's disease , 2009, Indian journal of psychiatry.

[24]  G. Halliday,et al.  Patients with vascular dementia due to microvascular pathology have significant hippocampal neuronal loss , 2002, Journal of neurology, neurosurgery, and psychiatry.