Neuropathology of Alzheimer Disease. Connections with cerebral senescence
September 18, 2011
Neuropathology of Alzheimer Disease. Connections with cerebral senescence
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Title: | Neuropathology of Alzheimer Disease. Connections with cerebral senescence |
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Article_Title: | Neuropathology of Alzheimer Disease. Connections with cerebral senescence |
Authors: | Dan Riga1*, Sorin Riga1, Aurel Ardelean2, George Pribac2, Francisc Schneider2 |
Affiliation: | 1 Department of Stress Research and Prophylaxis, ”Al. Obregia” Clinical Hospital of Psychiatry, Bucharest, Romania 2 ”Vasile Goldis” Western University, Arad, Romania |
Abstract: | Introduction. Alzheimer disease (AD) becomes ”disease of the century” by its prevalence, morbidity, prediction and economic impact. Paper aims of present and our following studies on AD were represented by the achievement of a global and unitarian bio-medical research of this inflammatory-degenerative pathology, the description of AD alterations in brain structures and by the correlation with the same changes from cerebral senescence. Materials and methods. Human brains from AD patients and old people, as well as aging brains from Wistar rats and guinea pigs were investigated by macro- and microscopic morphological methods. Results and Discussions. In AD patients, gross, imagistic and sectional anatomy revealed severe diffuse cortical atrophy (gyral narrowing and sulcal widening), ventricular dilatation and intense atrophy of the hippocampus and amygdala. Using microscopic anatomy, histology and cytology investigations, as AD structural hallmarks, we observed neuronal loss, amyloid plaques and neurofibrillary tangles, especially in cerebral cortex, hippocampus, amygdala and nucleus basalis of Meynert. In addition, we found neuropil threads, vascular amyloidosis, granulo-vacuolar degeneration, Hirano and Lewy bodies. All these neuropathological changes coexist with important lipopigment storages (lipofuscin and ceroid), landmarks of brain aging. The same modifications are presented in old human and animal brains, but much more reduced as number and intensity. Authors discuss the epistemological evolution of these pathological structural concepts and their pathophysiological significance. Conclusions. This study is the first Romanian research, where AD brains were investigated from anatomo-histologico-tissual level to cellular-subcellular and extracellular pathology. Also, the authors achieved a comparative and correlative research between AD and old brains from humans to animals. |
Keywords: | Alzheimer disease, cerebral senescence, neuropathology, morphological correlations, selective brain atrophy, amyloid plaques, neurofibrillary tangles, ceroid and lipofuscin pigments |
References: | Akashi T, Maruyama N, Sawayama N. An autopsy case of idiopathic parkinsonism with numerous Lewy bodies in the cerebral cortex – diffuse Lewy body disease. Brain and Nerve, 43: 175-181, 1991. American Psychiatric Association. DSM-IV-TR. Diagnostic and Statistical Manual of Mental Disorders. Forth Edition Text Revision. American Psychiatric Association, Washington, DC, 2000. Alzheimer A. Histologische Studien zur Differentialdiagnose der progressiven Paralyse. Fischer, Jena, DE, 1904. Alzheimer A. Über einen eigenartigen schweren Erkrankungsprozeß der Hirnrinde. Neurologisches Centralblatt, Leipzig, DE, 23: 1129-1136, 1906. Alzheimer A. Über eine eigenartige Erkrankung der Hirnrinde. Allg Z Psychiat, 64: 146-148, 1907. Anderson DM (ed). Dorland’s Illustrated Medical Dictionary, 30th ed. Elsevier-Saunders, Philadelphia, PA, 2003. Ball MJ. Hippocampal histopathology – a critical substrate for dementia of the Alzheimer type, pp. 16-37. In: S Ulrich (ed). Histology and Histopathology of the Aging Brain (HP von Hahn, ed Interdisciplinary Topics in Gerontology, vol 25). Karger, Basel, CH, 1988. Blocq P, Marinescu G. Sur les lésions et la pathogénie de l’épilepsie dite essentielle. Sem Méd, 12: 445-446, 1892. Bonin-Guillaume S, Zekry D, Giacobini E, Gold G, Michel JP. Impact économique de la démence. Presse Méd, 34: 35-41, 2005. Braak H, Braak E. Morphology of the human isocortex in young and aged individuals: qualitative and quantitative findings, pp. 1-15. In: J Ulrich (ed), Histology and Histopathology of the Aging Brain (HP von Hahn ed, Interdisciplinary Topics in Gerontology, vol 25). Karger, Basel, CH, 1988. Brookmeyer R, Johnson E, Ziegler-Graham K, Arrighi HM. Forecasting the global burden of Alzheimer’s disease. Alzheimer’s and Dementia, 3: 186-191, 2007. Esiri MM, Hyman BT, Beyreuther K, Masters CL. Ageing and dementia, pp. 153-233. In: DI Graham, PL Lantos (eds). Greenfield’s Neuropathology, 6th ed. Arnold, London, UK, 1997. Esiri MM, Morris JH. The Neuropathology of Dementia. Cambridge University Press, Cambridge, UK, 1997. Esquirol JED. Des maladies mentales considérées sous les rapports médical, hygiénique et médicolégal. Baillière, Paris, FR, 1830. Fischer O. Miliare Nekrosen mit drusigen Wucherungen der Neurofibrillen, eine regelmässige Veränderung der Hirnrinde bei seniler Demenz. Monatsschr Psychiat Neurol, 22: 361-372, 1907. Forno LS, The Lewy body in Parkinson’s disease. Adv Neurol, 45: 398-414, 1986. Gibson PH, Tomlinson BE. The numbers of Hirano bodies in the hippocampus of normal and demented subjects with Alzheimer’s disease. J Neurol Sci, 33: 199-206, 1977. Goedert M. Tau protein and the neurofibrillary pathology of Alyheimer’s disease. Trends Neurosci, 16: 460- 465, 1993. Hirano A. Pathology of amyotrophic lateral sclerosis, pp. 23-37. In: DC Gajdusek, CJ Gibbs, Jr (eds). Slow Latent and Temperate Virus Infections, NINDB Monograph No 2. National Institutes of Health, Bethesda, MD, 1965. Hirano A, Malamud N, Elizan TS, Kurland LT. Amyotrophic lateral sclerosis and Parkinsonismdementia complex on Guam. Arch Neurol, 15: 35- 51, 1966. Hirano A. Hirano bodies and related neuronal inclusions. Neurophatol Appl Neurobiol, 20: 3-11, 1994. Kraepelin E. Psychiatrie. Ein Lehrbuch für Studierende und Ärzte, 8 Auflage, Band II (Klinische Psychiatrie). Johann Ambrosius Barth Verlag, Leipzig, DE, 1910. Lennox G. Lewy body dementia. Bailliere’s Clin Neurol, 1: 653-676, 1992. Lewy FH. Paralysis agitans. 1. Pathologische anatomie, pp. 920-933. In: M Lewandowsky (ed.), Handbuch der Neurologie. Springer, Berlin, DE, 1912. Mann DMA, Neary D, Testa H. Color Atlas and Text of Adult Dementias. Mosby-Wolfe, London, UK, 1994. Marinesco G. La cellule nerveuse, vol 1 et vol 2, Octave Doin et Fils Éd, Paris, FR, 1909. Mayeux R, Stern Y, Spantos S. Heterogeneity in dementia of the Alzheimer type. Neurology, 35: 435-461, 1985. McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM. Clinical diagnosis of Alzheimer’s disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease. Neurology, 34: 939- 944, 1984. Nissl F. Zum Andenken A. Alzheimers. All Z Psychiat, 73: 96-107, 1916. Racchi M, Govoni S. The farmacology of amyloid precursor protein processing. Exp Gerontol, 38: 145-157, 2003. Rewcastle NB. Degenerative diseases of the central nervous system, pp. 904-961. In: RL Davis, DM Robertson (eds). Textbook of Neuropathology, 2nd ed. Williams & Wilkins, Baltimore, MD, 1991. Riga D, Riga S. Lipofuscin and ceroid pigments in aging and brain pathology. A review. I. Biochemical and morphological properties. Rom J Neurol Psychiat, 33: 121-136, 1995. Riga D, Riga S, Hălălău F, Schneider F. Brain lipopigment accumulation in normal and pathological aging, pp. 158- 163. In: SIS Rattan, P Kristensen, BFC Clark (eds), Understanding and Modulating Aging (Ann New York Acad Sci, vol 1067). Blackwell, Boston, MA, 2006a. Riga D, Riga S, Hălălău F, Schneider F. Lipofuscin and ceroid pigments – markers of normal and pathological brain aging, pp. 213-221. In: R Klatz, R Goldman (eds), Anti-Aging Therapeutics, vol. 8. American Academy of Anti-Aging Medicine (A4M), Chicago, IL, 2006b. Riga D, Riga S, Ardelean A, Hermenean A, Schneider F. Leziuni neuro-degenerative în boala Alzheimer şi în patologia asociată îmbătrânirii. A 27-a Sesiune Ştiinţifică Anuală a Societăţii Române de Biologie Celulară, Bistriţa, 11-14 iunie, 2009; Buletinul Societăţii Române de Biologie Celulară, 37: 25, 2009a. Riga S, Riga D, Hermenean A, Ardelean A, Schneider F. Modificări neuro-degenerative în îmbătrânire. A 27-a Sesiune Ştiinţifică Anuală a Societăţii Române de Biologie Celulară, Bistriţa, 11-14 iunie, 2009; Buletinul Societăţii Române de Biologie Celulară, 37: 26, 2009b. Riga S, Riga D, Pribac G, Ardelean A, Schneider F. Neuropathology of aging. Relations with Alzheimer disease. Studia Universitatis Vasile Goldiş. Life Science Series, 20: in press, 2010. Scholz W. Studien zur Pathologie der Hirngefässe. II. Die drusige Entartung der Hirnarterien und Kapillaren. Z ges Neurol Pschiat, 162: 694-715, 1938. Simchowicz T. Histologische Studien über die senile Demenz. Histol Histopathol Arbeit Grosshirnde, 4: 267-444, 1911. Summers WK, Korneva HA. Alzheimer’s disease – oxidative injury and cytokines, pp. 91-93. In: MD Binder, N Hirokawa, U Windhorst (eds). Encyclopedia of Neuroscience, Vol. 1(A-C). Springer, Berlin, DE, 2009. St George-Hyslop PH, Tanzi RE, Polinsky RJ, Haines JL, Nee L, Watkins PC, Myers RH, Feldman RG, Pollen D, Drachman D et al. The genetic defect causing familial Alzheimer’s disease maps on chromosome 21. Science, 235: 885-890, 1987. Trojanowski JQ, Schmidt ML, Shin R-W, Bramblett GT, Rao D, Lee VM-Y. PHFτ(A68): from pathological marker to potential mediator of neuronal dysfunction and neuronal degeneration in Alzheimer’s disease. Clin Neurosci, 1: 184-191, 1993. World Health Organization. The ICD-10 Classification of Mental and Behavioural Disorders. Clinical Descriptions and Diagnostic Guidelines. World Health Organization, Geneva, 1992. Bucharest, 2004. |
Read_full_article: | pdf/21-2011/21-2-2011/SU21-2-2011Riga.pdf |
Correspondence: | Dan Riga, Department Of Stress Research And Prophylaxis, ”Al. Obregia” Clinical Hospital Of Psychiatry, 10 Berceni Rd., 041914 Bucharest 8, Romania, Tel. +40 21 334 3008, Fax +40 21 230 95 79, Email: d_s_riga@yahoo.com |
Read full article | |
Article Title: | Neuropathology of Alzheimer Disease. Connections with cerebral senescence |
Authors: | Dan Riga1*, Sorin Riga1, Aurel Ardelean2, George Pribac2, Francisc Schneider2 |
Affiliation: | 1 Department of Stress Research and Prophylaxis, ”Al. Obregia” Clinical Hospital of Psychiatry, Bucharest, Romania 2 ”Vasile Goldis” Western University, Arad, Romania |
Abstract: | Introduction. Alzheimer disease (AD) becomes ”disease of the century” by its prevalence, morbidity, prediction and economic impact. Paper aims of present and our following studies on AD were represented by the achievement of a global and unitarian bio-medical research of this inflammatory-degenerative pathology, the description of AD alterations in brain structures and by the correlation with the same changes from cerebral senescence. Materials and methods. Human brains from AD patients and old people, as well as aging brains from Wistar rats and guinea pigs were investigated by macro- and microscopic morphological methods. Results and Discussions. In AD patients, gross, imagistic and sectional anatomy revealed severe diffuse cortical atrophy (gyral narrowing and sulcal widening), ventricular dilatation and intense atrophy of the hippocampus and amygdala. Using microscopic anatomy, histology and cytology investigations, as AD structural hallmarks, we observed neuronal loss, amyloid plaques and neurofibrillary tangles, especially in cerebral cortex, hippocampus, amygdala and nucleus basalis of Meynert. In addition, we found neuropil threads, vascular amyloidosis, granulo-vacuolar degeneration, Hirano and Lewy bodies. All these neuropathological changes coexist with important lipopigment storages (lipofuscin and ceroid), landmarks of brain aging. The same modifications are presented in old human and animal brains, but much more reduced as number and intensity. Authors discuss the epistemological evolution of these pathological structural concepts and their pathophysiological significance. Conclusions. This study is the first Romanian research, where AD brains were investigated from anatomo-histologico-tissual level to cellular-subcellular and extracellular pathology. Also, the authors achieved a comparative and correlative research between AD and old brains from humans to animals. |
Keywords: | Alzheimer disease, cerebral senescence, neuropathology, morphological correlations, selective brain atrophy, amyloid plaques, neurofibrillary tangles, ceroid and lipofuscin pigments |
References: | Akashi T, Maruyama N, Sawayama N. An autopsy case of idiopathic parkinsonism with numerous Lewy bodies in the cerebral cortex – diffuse Lewy body disease. Brain and Nerve, 43: 175-181, 1991. American Psychiatric Association. DSM-IV-TR. Diagnostic and Statistical Manual of Mental Disorders. Forth Edition Text Revision. American Psychiatric Association, Washington, DC, 2000. Alzheimer A. Histologische Studien zur Differentialdiagnose der progressiven Paralyse. Fischer, Jena, DE, 1904. Alzheimer A. Über einen eigenartigen schweren Erkrankungsprozeß der Hirnrinde. Neurologisches Centralblatt, Leipzig, DE, 23: 1129-1136, 1906. Alzheimer A. Über eine eigenartige Erkrankung der Hirnrinde. Allg Z Psychiat, 64: 146-148, 1907. Anderson DM (ed). Dorland’s Illustrated Medical Dictionary, 30th ed. Elsevier-Saunders, Philadelphia, PA, 2003. Ball MJ. Hippocampal histopathology – a critical substrate for dementia of the Alzheimer type, pp. 16-37. In: S Ulrich (ed). Histology and Histopathology of the Aging Brain (HP von Hahn, ed Interdisciplinary Topics in Gerontology, vol 25). Karger, Basel, CH, 1988. Blocq P, Marinescu G. Sur les lésions et la pathogénie de l’épilepsie dite essentielle. Sem Méd, 12: 445-446, 1892. Bonin-Guillaume S, Zekry D, Giacobini E, Gold G, Michel JP. Impact économique de la démence. Presse Méd, 34: 35-41, 2005. Braak H, Braak E. Morphology of the human isocortex in young and aged individuals: qualitative and quantitative findings, pp. 1-15. In: J Ulrich (ed), Histology and Histopathology of the Aging Brain (HP von Hahn ed, Interdisciplinary Topics in Gerontology, vol 25). Karger, Basel, CH, 1988. Brookmeyer R, Johnson E, Ziegler-Graham K, Arrighi HM. Forecasting the global burden of Alzheimer’s disease. Alzheimer’s and Dementia, 3: 186-191, 2007. Esiri MM, Hyman BT, Beyreuther K, Masters CL. Ageing and dementia, pp. 153-233. In: DI Graham, PL Lantos (eds). Greenfield’s Neuropathology, 6th ed. Arnold, London, UK, 1997. Esiri MM, Morris JH. The Neuropathology of Dementia. Cambridge University Press, Cambridge, UK, 1997. Esquirol JED. Des maladies mentales considérées sous les rapports médical, hygiénique et médicolégal. Baillière, Paris, FR, 1830. Fischer O. Miliare Nekrosen mit drusigen Wucherungen der Neurofibrillen, eine regelmässige Veränderung der Hirnrinde bei seniler Demenz. Monatsschr Psychiat Neurol, 22: 361-372, 1907. Forno LS, The Lewy body in Parkinson’s disease. Adv Neurol, 45: 398-414, 1986. Gibson PH, Tomlinson BE. The numbers of Hirano bodies in the hippocampus of normal and demented subjects with Alzheimer’s disease. J Neurol Sci, 33: 199-206, 1977. Goedert M. Tau protein and the neurofibrillary pathology of Alyheimer’s disease. Trends Neurosci, 16: 460- 465, 1993. Hirano A. Pathology of amyotrophic lateral sclerosis, pp. 23-37. In: DC Gajdusek, CJ Gibbs, Jr (eds). Slow Latent and Temperate Virus Infections, NINDB Monograph No 2. National Institutes of Health, Bethesda, MD, 1965. Hirano A, Malamud N, Elizan TS, Kurland LT. Amyotrophic lateral sclerosis and Parkinsonismdementia complex on Guam. Arch Neurol, 15: 35- 51, 1966. Hirano A. Hirano bodies and related neuronal inclusions. Neurophatol Appl Neurobiol, 20: 3-11, 1994. Kraepelin E. Psychiatrie. Ein Lehrbuch für Studierende und Ärzte, 8 Auflage, Band II (Klinische Psychiatrie). Johann Ambrosius Barth Verlag, Leipzig, DE, 1910. Lennox G. Lewy body dementia. Bailliere’s Clin Neurol, 1: 653-676, 1992. Lewy FH. Paralysis agitans. 1. Pathologische anatomie, pp. 920-933. In: M Lewandowsky (ed.), Handbuch der Neurologie. Springer, Berlin, DE, 1912. Mann DMA, Neary D, Testa H. Color Atlas and Text of Adult Dementias. Mosby-Wolfe, London, UK, 1994. Marinesco G. La cellule nerveuse, vol 1 et vol 2, Octave Doin et Fils Éd, Paris, FR, 1909. Mayeux R, Stern Y, Spantos S. Heterogeneity in dementia of the Alzheimer type. Neurology, 35: 435-461, 1985. McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM. Clinical diagnosis of Alzheimer’s disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease. Neurology, 34: 939- 944, 1984. Nissl F. Zum Andenken A. Alzheimers. All Z Psychiat, 73: 96-107, 1916. Racchi M, Govoni S. The farmacology of amyloid precursor protein processing. Exp Gerontol, 38: 145-157, 2003. Rewcastle NB. Degenerative diseases of the central nervous system, pp. 904-961. In: RL Davis, DM Robertson (eds). Textbook of Neuropathology, 2nd ed. Williams & Wilkins, Baltimore, MD, 1991. Riga D, Riga S. Lipofuscin and ceroid pigments in aging and brain pathology. A review. I. Biochemical and morphological properties. Rom J Neurol Psychiat, 33: 121-136, 1995. Riga D, Riga S, Hălălău F, Schneider F. Brain lipopigment accumulation in normal and pathological aging, pp. 158- 163. In: SIS Rattan, P Kristensen, BFC Clark (eds), Understanding and Modulating Aging (Ann New York Acad Sci, vol 1067). Blackwell, Boston, MA, 2006a. Riga D, Riga S, Hălălău F, Schneider F. Lipofuscin and ceroid pigments – markers of normal and pathological brain aging, pp. 213-221. In: R Klatz, R Goldman (eds), Anti-Aging Therapeutics, vol. 8. American Academy of Anti-Aging Medicine (A4M), Chicago, IL, 2006b. Riga D, Riga S, Ardelean A, Hermenean A, Schneider F. Leziuni neuro-degenerative în boala Alzheimer şi în patologia asociată îmbătrânirii. A 27-a Sesiune Ştiinţifică Anuală a Societăţii Române de Biologie Celulară, Bistriţa, 11-14 iunie, 2009; Buletinul Societăţii Române de Biologie Celulară, 37: 25, 2009a. Riga S, Riga D, Hermenean A, Ardelean A, Schneider F. Modificări neuro-degenerative în îmbătrânire. A 27-a Sesiune Ştiinţifică Anuală a Societăţii Române de Biologie Celulară, Bistriţa, 11-14 iunie, 2009; Buletinul Societăţii Române de Biologie Celulară, 37: 26, 2009b. Riga S, Riga D, Pribac G, Ardelean A, Schneider F. Neuropathology of aging. Relations with Alzheimer disease. Studia Universitatis Vasile Goldiş. Life Science Series, 20: in press, 2010. Scholz W. Studien zur Pathologie der Hirngefässe. II. Die drusige Entartung der Hirnarterien und Kapillaren. Z ges Neurol Pschiat, 162: 694-715, 1938. Simchowicz T. Histologische Studien über die senile Demenz. Histol Histopathol Arbeit Grosshirnde, 4: 267-444, 1911. Summers WK, Korneva HA. Alzheimer’s disease – oxidative injury and cytokines, pp. 91-93. In: MD Binder, N Hirokawa, U Windhorst (eds). Encyclopedia of Neuroscience, Vol. 1(A-C). Springer, Berlin, DE, 2009. St George-Hyslop PH, Tanzi RE, Polinsky RJ, Haines JL, Nee L, Watkins PC, Myers RH, Feldman RG, Pollen D, Drachman D et al. The genetic defect causing familial Alzheimer’s disease maps on chromosome 21. Science, 235: 885-890, 1987. Trojanowski JQ, Schmidt ML, Shin R-W, Bramblett GT, Rao D, Lee VM-Y. PHFτ(A68): from pathological marker to potential mediator of neuronal dysfunction and neuronal degeneration in Alzheimer’s disease. Clin Neurosci, 1: 184-191, 1993. World Health Organization. The ICD-10 Classification of Mental and Behavioural Disorders. Clinical Descriptions and Diagnostic Guidelines. World Health Organization, Geneva, 1992. Bucharest, 2004. |
*Correspondence: | Dan Riga, Department Of Stress Research And Prophylaxis, ”Al. Obregia” Clinical Hospital Of Psychiatry, 10 Berceni Rd., 041914 Bucharest 8, Romania, Tel. +40 21 334 3008, Fax +40 21 230 95 79, Email: d_s_riga@yahoo.com |