The intralaminar nuclei assigned to the medial pain system and other components of this system are early and progressively affected by the Alzheimer's disease-related cytoskeletal pathology

The intralaminar nuclei of the human thalamus are integrated into the ascending reticular activating system and into limbic, oculomotor and somatomotor loops. In addition, some of them also represent important components of the medial pain system. We examined the occurrence and severity of the Alzheimer's disease (AD)-related cytoskeletal pathology and beta-amyloidosis in the seven intralaminar nuclei (central lateral nucleus, CL; central medial nucleus, CEM; centromedian nucleus, CM; cucullar nucleus, CU; paracentral nucleus, PC; parafascicular nucleus, PF; subparafascicular nucleus, SPF) in 27 autopsy cases at different stages of the cortical neurofibrillary pathology (cortical NFT/NT-stages I-VI) and beta-amyloidosis (cortical phases 1-4). The CEM, CL, PF, and SPF are slightly affected at stage II (corresponding to preclinical AD). They are markedly involved at stages III and IV (i.e. incipient AD) and severely affected at stages V and VI (i.e. clinical AD). In the PC and CU, the cytoskeletal pathology is mild at stage III, marked at stage IV, and severe at stages V-VI, whereas the CM is only mildly affected at stages IV-VI. In all of the intralaminar nuclei, deposits of the protein beta-amyloid occur for the first time during the final phase of cortical beta-amyloidosis. Functionally, the cytoskeletal pathology encountered in the intralaminar nuclei may contribute to the memory and affective symptoms, attention deficits, and dysfunctions related to horizontal saccades and smooth pursuits seen in AD patients. Equally important, however, are the findings that the cytoskeletal pathology developing within the intralaminar nuclei assigned to the medial pain system (CEM, CL, CU, PC, PF) as well as within other components of this system begins already during the preclinical or incipient phases of AD. Given this fact, the question arises as to whether non-discriminative aspects mediated by the medial pain system could be employed to identify individuals in the very earliest stages of AD.

[1]  W A Fletcher,et al.  Smooth pursuit dysfunction in Alzheimer's disease , 1988, Neurology.

[2]  M. Mesulam,et al.  From sensation to cognition. , 1998, Brain : a journal of neurology.

[3]  H. Braak,et al.  Early involvement of the tegmentopontine reticular nucleus during the evolution of Alzheimer’s disease-related cytoskeletal pathology , 2001, Brain Research.

[4]  G. Martin 8 – Reticular Formation of the Pons and Medulla , 1990 .

[5]  J. Hodges,et al.  Attention and executive deficits in Alzheimer's disease. A critical review. , 1999, Brain : a journal of neurology.

[6]  B. Vogt,et al.  Anterior Cingulate Cortex and the Medial Pain System , 1993 .

[7]  G. E. Alexander,et al.  Basal ganglia-thalamocortical circuits: parallel substrates for motor, oculomotor, "prefrontal" and "limbic" functions. , 1990, Progress in brain research.

[8]  E. Scherder,et al.  Alzheimer patients report less pain intensity and pain affect than non-demented elderly. , 1999, Psychiatry.

[9]  G Gainotti,et al.  A double dissociation between accuracy and time of execution on attentional tasks in Alzheimer's disease and multi-infarct dementia. , 2001, Brain : a journal of neurology.

[10]  A. Damasio,et al.  Selective pathological changes of the periaqueductal gray in Alzheimer's disease , 2000, Neurobiology of Aging.

[11]  M M Mesulam,et al.  Cholinergic innervation of the human thalamus: Dual origin and differential nuclear distribution , 1992, The Journal of comparative neurology.

[12]  K. Jellinger,et al.  Neuropathological staging of Alzheimer lesions and intellectual status in Alzheimer's and Parkinson's disease patients , 1993, Neuroscience Letters.

[13]  J. Price,et al.  Diagnostic Criteria for Alzheimer’s Disease , 1997, Neurobiology of Aging.

[14]  H. Braak,et al.  A sequence of cytoskeleton changes related to the formation of neurofibrillary tangles and neuropil threads , 2004, Acta Neuropathologica.

[15]  J. Voogd,et al.  The human central nervous system , 1978 .

[16]  H. Braak,et al.  Demonstration of Amyloid Deposits and Neurofibrillary Changes in Whole Brain Sections , 1991, Brain pathology.

[17]  Igor A. Ilinsky,et al.  Limbic Thalamus: Structure, Intrinsic Organization, and Connections , 1993 .

[18]  A. Parent,et al.  Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: A PHA‐L study of subcortical projections , 1992, The Journal of comparative neurology.

[19]  R. Helme,et al.  The impact of dementia on the pain experience , 1996, PAIN.

[20]  W. Markesbery Neuropathology of dementing disorders , 1998 .

[21]  F. Benedetti,et al.  Autonomic responses and pain perception in Alzheimer’s disease , 2000, European journal of pain.

[22]  G. V. Van Hoesen,et al.  Selective pathological changes of the periaqueductal gray matter in Alzheimer's disease , 2000, Annals of neurology.

[23]  J. Trojanowski,et al.  Editorial on Consensus Recommendations for the Postmortem Diagnosis of Alzheimer Disease from the National Institute on Aging and the Reagan Institute Working Group on Diagnostic Criteria for the Neuropathological Assessment of Alzheimer Disease , 1997, Journal of neuropathology and experimental neurology.

[24]  M. Gabriel,et al.  Neurobiology of Cingulate Cortex and Limbic Thalamus , 1993 .

[25]  G. Zaccara,et al.  Smooth-pursuit eye movements: alterations in Alzheimer's disease , 1992, Journal of the Neurological Sciences.

[26]  J. Bortz,et al.  Verteilungsfreie Methoden in der Biostatistik , 1982 .

[27]  J. Hardy,et al.  Alzheimer's disease: the amyloid cascade hypothesis. , 1992, Science.

[28]  J. Morris,et al.  Dementia and response to pain in the elderly , 1996, Pain.

[29]  J. Ulrich,et al.  Alzheimer's Disease: A Description of the Structural Lesions , 1991, Brain pathology.

[30]  G. Kuchel,et al.  Neurotrophin receptor and tyrosine hydroxylase gene expression in aged sympathetic neurons , 1997, Neurobiology of Aging.

[31]  H. Buschke,et al.  Memory and mental status correlates of modified Braak staging , 1999, Neurobiology of Aging.

[32]  M. Kunik,et al.  Assessment and understanding of pain in patients with dementia. , 2000, The Gerontologist.

[33]  Ove Almkvist,et al.  Early diagnosis of Alzheimer dementia based on clinical and biological factors , 1999, European Archives of Psychiatry and Clinical Neuroscience.

[34]  B. Gulyás,et al.  Activation by Attention of the Human Reticular Formation and Thalamic Intralaminar Nuclei , 1996, Science.

[35]  A. Gellatly,et al.  The experience and expression of pain in Alzheimer patients. , 1997, Age and ageing.

[36]  H. Braak,et al.  Sequence of Aβ‐Protein Deposition in the Human Medial Temporal Lobe , 2000 .

[37]  E. G. Jones,et al.  A new parcellation of the human thalamus on the basis of histochemical staining , 1989, Brain Research Reviews.

[38]  H. Braak,et al.  Parkinson’s disease: the thalamic components of the limbic loop are severely impaired by α-synuclein immunopositive inclusion body pathology , 2002, Neurobiology of Aging.

[39]  H. Braak,et al.  Diagnostic Criteria for Neuropathologic Assessment of Alzheimer’s Disease , 1997, Neurobiology of Aging.

[40]  H. Braak,et al.  Neuropathological stageing of Alzheimer-related changes , 2004, Acta Neuropathologica.

[41]  J. Sharpe,et al.  Saccadic eye movement dysfunction in Alzheimer's disease , 1986, Annals of neurology.

[42]  E. Scherder,et al.  Visual Analogue Scales for Pain Assessment in Alzheimer’s Disease , 1999, Gerontology.

[43]  A. Morel,et al.  Multiarchitectonic and stereotactic atlas of the human thalamus , 1997, The Journal of comparative neurology.

[44]  A. Eschalier,et al.  Pain and Alzheimer’s Disease , 2000, Gerontology.

[45]  H. Braak,et al.  The premotor region essential for rapid vertical eye movements shows early involvement in Alzheimer's disease-related cytoskeletal pathology , 2001, Vision Research.

[46]  H. Braak,et al.  The autonomic higher order processing nuclei of the lower brain stem are among the early targets of the Alzheimer's disease-related cytoskeletal pathology , 2001, Acta Neuropathologica.

[47]  D. German,et al.  Alzheimer's disease: Neurofibrillary tangles in nuclei that project to the cerebral cortex , 1987, Neuroscience.

[48]  B. Vogt,et al.  The medial pain system, cingulate cortex, and parallel processing of nociceptive information. , 2000, Progress in brain research.

[49]  F. Benedetti,et al.  Pain threshold and tolerance in Alzheimer's disease , 1999, Pain.

[50]  Hans Förstl,et al.  Clinical features of Alzheimer’s disease , 1999, European Archives of Psychiatry and Clinical Neuroscience.

[51]  H. Groenewegen,et al.  The specificity of the ‘nonspecific’ midline and intralaminar thalamic nuclei , 1994, Trends in Neurosciences.

[52]  G. V. Van Hoesen,et al.  Severe pathological changes of parabrachial nucleus in Alzheimer's disease , 1998, Neuroreport.

[53]  B. Reisberg,et al.  The neurologic syndrome of severe Alzheimer's disease. Relationship to functional decline. , 1993, Archives of neurology.

[54]  R. Leigh,et al.  The neurology of eye movements , 1984 .