Increased frequency of dentate granule cells with basal dendrites in the hippocampal formation of schizophrenics

Psychiatry Research - Neuroimaging

Volumn 122, Issue 2, 2003, Pages 89-97

  Lauer, Martin ^a   Beckmann, Helmut ^a   Senitz, Dieter ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

Adult neurogenesis; Dentate gyrus; Entorhinal cortex; Hippocampus; Migration disorder; Neuroplasticity; Prenatal maldevelopement

Indexed keywords

ADULT; AGED; ARTICLE; BRAIN DEVELOPMENT; CELL STRUCTURE; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOARCHITECTURE; DENDRITE; DENTATE GYRUS; DEVELOPMENTAL DISORDER; ENTORHINAL CORTEX; FEMALE; GOLGI COMPLEX; GRANULE CELL; HIPPOCAMPUS; HUMAN; HUMAN TISSUE; LIMBIC CORTEX; MALE; PRENATAL DEVELOPMENT; PRIORITY JOURNAL; SCHIZOPHRENIA;

AGED; AGED, 80 AND OVER; BRAIN DAMAGE, CHRONIC; CELL COUNT; CELL MOVEMENT; DENDRITES; DENTATE GYRUS; ENTORHINAL CORTEX; FEMALE; HIPPOCAMPUS; HUMANS; INTERNEURONS; MALE; MIDDLE AGED; NEURONAL PLASTICITY; REFERENCE VALUES; SCHIZOPHRENIA;

EID: 0037441696     PISSN: 09254927     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4927(02)00122-1     Document Type: Article

References (52)

1. Akbarian S., Vinuela A., Kim J.J., Potkin S.G., Bunney W.E. Jr., Jones E.G. Distorted distribution of nicotinamide-adenine-diaphorase neurons in temporal lobe of schizophrenics implies anomalous cortical development. Archives of General Psychiatry. 50:1993;169-187.
2. Akil M., Lewis D.A. Cytoarchitecture of the entorhinal cortex in schizophrenia. American Journal of Psychiatry. 154:1997;1010-1012.
3. Akil M., Edgar C.L., Pierri J.N., Casali S., Lewis D.A. Decreased density of tyrosine hydroxylase-immunoreactive axons in the entorhinal cortex of schizophrenic subjects. Biological Psychiatry. 47:2000;361-370.
4. Alexander G.E., DeLong M.R., Strick P.L. Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annual Review of Neuroscience. 9:1986;357-381.
5. Arnold S.E., Hyman B.T., Van Hoesen G.W., Damasio A.R. Some cytoarchitectural abnormalities of the entorhinal cortex in schizophrenia. Archives of General Psychiatry. 48:1991;625-632.
6. Arnold S.E., Ruscheinsky D.D., Han L.Y. Further evidence of abnormal cytoarchitecture of the entorhinal cortex in schizophrenia using spatial point pattern analyses. Biological Psychiatry. 42:1997;639-647.
7. Arnold S.E., Trojanowski J.Q. Recent advances in defining the neuropathology of schizophrenia. Acta Neuropathologica. 92:1996;217-231.
8. Arnold S.E. Cellular and molecular neuropathology of the parahippocampal region in schizophrenia. Annals of the New York Academy of Sciences. 911:2000;275-292.
9. Beckmann H. Neuropathology of the endogenous psychoses. Henn F., Sartorius N., Helmchen H., Lauter H. Contemporary Psychiatry. 3:2001;81-101 Springer Verlag, Berlin and New York.
10. Beckmann H., Jakob H. Prenatal disturbances of nerve cell migration in the entorhinal region: a common vulnerability factor in functional psychoses? Journal of Neural Transmission. 84:1991;155-164.
11. Bernstein H.G., Krell D., Baumann B., Danos P., Falkai P., Diekmann S., Henning H., Bogerts B. Morphometric studies of the entorhinal cortex in neuropsychiatric patients and controls: clusters of heterotopically displaced lamina II neurons are not indicative of schizophrenia. Schizophrenia Research. 33:1998;125-132.
12. Braak H., Braak E. The human entorhinal cortex: normal morphology and lamina-specific pathology in various diseases. Neuroscience Research. 15:1992;6-31.
13. Braak H., Braak E., Yilmazer D., de Vos R.A., Jansen E.N., Bohl J. Pattern of brain destruction in Parkinson's and Alzheimer's diseases. Journal of Neural Transmission. 103:1996;455-490.
14. Bubenaite J. Ber einige Erfahrungen mit der Golgi-Methode. Zeitschrift für wissenschaftiche Mikroskopie. 46:1929;359-360.
15. Buchsbaum M.S. Frontal lobes, basal ganglia, temporal lobes - three sites for schizophrenia? Schizophrenia Bulletin. 16:1990;377-378.
16. Cameron H.A., McEwen B.S., Gould E. Regulation of adult neurogenesis by excitatory input and NMDA receptor activation in the dentate gyrus. Journal of Neuroscience. 15:1995;4687-4692.
17. Csernansky J.G., Bardgett M.E. Limbic-cortical neuronal damage and the pathophysiology of schizophrenia. Schizophrenia Bulletin. 24:1998;231-248.
18. Dawirs R.R., Hildebrandt K., Teuchert-Noodt G. Adult treatment with haloperidol increases dentate granule cell proliferation in the gerbil hippocampus. Journal of Neural Transmission. 105:1998;317-327.
19. Duffy C.J., Rakic P. Differentiation of granule cell dendrites in the dentate gyrus of the rhesus monkey: a quantitative Golgi study. Journal of Comparative Neurology. 214:1983;224-237.
20. Duman R.S. Synaptic plasticity and mood disorders. Molecular Psychiatry. 7:(Supplement 1):2002;S29-S43.
21. Erickson S.L., Akil M., Levey A.I., Lewis D.A. Postnatal development of tyrosine hydroxylase- and dopamine transporter-immunoreactive axons in monkey rostral entorhinal cortex. Cerebral Cortex. 8:1998;415-427.
22. Eriksson P.S., Perfilieva E., Bjork-Eriksson T., Alborn A.M., Nordborg C., Peterson D.A., Gage F.H. Neurogenesis in the adult human hippocampus. Nature Medicine. 4:1998;1-5.
23. Falkai P., Bogerts B., Rozumek M. Limbic pathology in schizophrenia: the entorhinal region - a morphometric study. Biological Psychiatry. 24:1988;515-521.
24. Falkai P., Schneider-Axmann T., Honer W.G. Entorhinal cortex pre-alpha cell clusters in schizophrenia: quantitative evidence of a developmental abnormality. Biological Psychiatry. 47:2000;937-943.
25. Gould E., Cameron H.A. Regulation of neuronal birth, migration and death in the rat dentate gyrus. Developmental Neuroscience. 18:1996;22-35.
26. Gould E., Cameron H.A., McEwen B.S. Blockade of NMDA receptors increases cell death and birth in the developing rat dentate gyrus. Journal of Comparative Neurology. 340:1994;551-565.
27. Gould, E., Reeves, A.J., Fallah, M., Tanapat, P., Gross, C.G., Fuchs, E. 1999. Hippocampal neurogenesis in adult Old World primates. Proceedings of the National Academy of Science USA 96, 5263-5267.
28. Harrison P.J., Roberts G.W. The Neuropathology of Schizophrenia. 2000;Oxford University Press, Oxford.
29. Jakob, H., Beckmann, H. 1984. Clinical-neuropathological studies of developmental disorders in the limbic system in chronic schizophrenia. In: Schizophrenia: An Integrative View. XIV CINP. Ricerca Scient. Educazione Permanente Supplement 39, p. 81.
30. Jakob H., Beckmann H. Prenatal developmental disturbances in the limbic allocortex in schizophrenics. Journal of Neural Transmission. 65:1986;303-326.
31. Jakob H., Beckmann H. Circumscribed malformation and nerve cell alterations in the entorhinal cortex of schizophrenics. Journal of Neural Transmission. 98:1994;83-106.
32. Karnovsky M.J. A formaldehyde-glutaraldehyde fixative of high osmolarity for use in electron microscopy. Journal of Cell Biology. 27:1965;137A-138A.
33. Kovelman J.A., Scheibel A.B. A neurohistological correlate of schizophrenia. Biological Psychiatry. 19:1984;1601-1619.
34. Krimer L.S., Herman M.M., Saunders R.C., Boyd J.C., Hyde T.M., Carter J.M., Kleinman J.E., Weinberger D.R. A qualitative and quantitative analysis of the entorhinal cortex in schizophrenia. Cerebral Cortex. 7:1997;732-739.
35. Malberg J.E., Eisch A.J., Nestler E.J., Duman R.S. Chronic antidepressant treatment increases neurogenesis in adult rat hippocampus. Neuroscience. 15:2000;9104-9110.
36. Markakis E.A., Gage F.H. Adult-generated neurons in the dentate gyrus send axonal projections to field CA3 and are surrounded by synaptic vesicles. Journal of Comparative Neurology. 406:1999;449-460.
37. Oppenheim R.W. Cell death during development of the nervous system. Annual Review of Neuroscience. 14:1991;453-501.
38. Parent J.M., Yu T.W., Leibowitz R.T., Geschwind D.H., Sloviter R.S., Lowenstein D.H. Dentate granule cell neurogenesis is increased by seizures and contributes to aberrant network reorganization in the adult rat hippocampus. Journal of Neuroscience. 17:1997;3727-3738.
39. Poduri A., Beason-Held L.L., Moss M.B., Rosene D.L., Hyman B.T. CA3 neuronal degeneration follows chronic entorhinal cortex lesions. Neuroscience Letters. 197:1995;1-4.
40. Senitz D. Über einen interkapillären Zelltyp im Hirn alter Menschen. Zentralblatt der Allgemeinen Pathologie und Pathologischen Anatomie. 122:1978;423-427.
41. Seress L. Morphological variability and developmental aspects of monkey and human granule cells: differences between the rodent and primate dentate gyrus. Epilepsy Research Supplement. 7:1992;3-28.
42. Seress L., Mrzljak L. Basal dendrites of granule cells are normal features of the fetal and adult dentate gyrus of both monkey and human hippocampal formations. Brain Research. 405:1987;169-174.
43. Seress L., Pokorny J. Structure of the granular layer of the rat dentate gyrus. A light microscopic and Golgi study. Journal of Anatomy. 133:1981;181-195.
44. Spigelman I., Yan X.X., Obenaus A., Lee E.Y., Wasterlain C.G., Ribak C.E. Dentate granule cells form novel basal dendrites in a rat model of temporal lobe epilepsy. Neuroscience. 86:1998;109-120.
45. Sutula T., Cascino G., Cavazos J., Parada I., Ramirez L. Mossy fiber synaptic reorganization in the epileptic human temporal lobe. Annals of Neurology. 26:1989;321-330.
46. Tömböl T., Somogyi G., Hajdu F. Golgi study on cat hippocampal formation. Anatomy and Embryology. 153:1978;331-350.
47. Vaidya V.A., Siuciak J.A., Du F., Duman R.S. Hippocampal mossy fiber sprouting induced by chronic electroconvulsive seizures. Neuroscience. 89:1999;157-166.
48. Van Hoesen G.W. The parahippocampal gyrus. New observations regarding its cortical connections in the monkey. Trends in Neuroscience. 5:1982;345-350.
49. von Campe G., Spencer D.D., de Lanerolle N.C. Morphology of dentate granule cells in the human epileptogenic hippocampus. Hippocampus. 7:1997;472-488.
50. Weinberger D.R. From neuropathology to neurodevelopment. The Lancet. 346:1995;552-557.
51. Weinberger D.R. Cell biology of the hippocampal formation in schizophrenia. Biological Psychiatry. 45:1999;395-402.
52. Yan X.X., Spigelman I., Tran P.H., Ribak C.E. Atypical features of rat dentate granule cells: recurrent basal dendrites and apical axons. Anatomy and Embryology. 203:2001;203-209.