Myelination of cortical-hippocampal relays during late adolescence.

The normal developmental series of brains in the Yakovlev Collection has been examined to explore the possibility that various brain regions implicated in schizophrenia may show changes in myelination during late adolescence, a period coinciding with the appearance of early symptoms of this disorder. The prefrontal, cingulate, and parahippocampal (entorhinal) cortex, as well as the perforant pathway, cingulum bundle, and hippocampus, were closely examined because these regions have recently been found to show various neuropathological differences in schizophrenia. Observation of these specimens has confirmed earlier reports by Yakovlev and Lecours (1967) that primary motor and sensory cortices show robust myelination early in the first decade of life. In contrast, associative cortical areas show increased amounts of myelin staining only by the second decade, although some cortical areas, like the cingulate and basofrontal cortex, remain poorly myelinated throughout life. The most striking finding, however, was the appearance of increased myelination of the subicular and presubicular regions during the late adolescent period. Increased myelination in the subiculum was localized to a discrete region at the surface where fibers of the perforant pathway are known to aggregate as they course toward the area dentata. The comparable region in the adjacent presubicular area that also showed increased myelin staining probably contains distal portions of the cingulum bundle. Support for this latter possibility was obtained from a single case in which a stereotaxically placed lesion causing interruption of the cingulum bundle showed less myelin in the presubicular area of the effectively lesioned side.(ABSTRACT TRUNCATED AT 250 WORDS)

[1]  E. Fifková,et al.  Two types of terminal degeneration in the molecular layer of the dentate fascia following lesions of the entorhinal cortex. , 1975, Brain research.

[2]  S. Finger,et al.  Early brain damage , 1984 .

[3]  E. Irle,et al.  Widespread cortical projections of the hippocampal formation in the cat , 1982, Neuroscience.

[4]  J. W. Papez A PROPOSED MECHANISM OF EMOTION , 1937 .

[5]  F. Benes,et al.  An analysis of the arrangement of neurons in the cingulate cortex of schizophrenic patients. , 1987, Archives of general psychiatry.

[6]  F. Mott ARCHIVES OF NEUROLOGY AND PSYCHIATRY , 1923 .

[7]  F. Benes,et al.  Quantitative cytoarchitectural studies of the cerebral cortex of schizophrenics. , 1986, Archives of general psychiatry.

[8]  P. Yakovlev,et al.  The myelogenetic cycles of regional maturation of the brain , 1967 .

[9]  D. Weinberger Implications of normal brain development for the pathogenesis of schizophrenia. , 1987, Archives of general psychiatry.

[10]  R. Murray,et al.  Is schizophrenia a neurodevelopmental disorder? , 1987, British medical journal.

[11]  M. T. Shipley,et al.  Presubiculum afferents to the entorhinal area and the Papez circuit. , 1974, Brain research.

[12]  T. Blackstad On the termination of some afferents to the hippocampus and fascia dentata; an experimental study in the rat. , 1958, Acta anatomica.

[13]  A. Hjorth-Simonsen,et al.  Some intrinsic connections of the hippocampus in the rat: An experimental analysis , 1973, The Journal of comparative neurology.

[14]  M. Mesulam,et al.  The functional anatomy and hemispheric specialization for directed attention The role of the parietal lobe and its connectivity , 1983, Trends in Neurosciences.

[15]  E. Fifkova´ Two types of terminal degeneration in the molecular layer of the dentate fascia following lesions of the entorhinal cortex , 1975, Brain Research.

[16]  A. Minkowski,et al.  Regional Development of the Brain in Early Life , 1968 .

[17]  F. Benes,et al.  Increased vertical axon numbers in cingulate cortex of schizophrenics. , 1987, Archives of general psychiatry.

[18]  B. Bogerts,et al.  Basal Ganglia and Limbic System Pathology in Schizophrenia: A Morphometric Study of Brain Volume and Shrinkage , 1985 .

[19]  G. Raisman,et al.  An experimental analysis of the efferent projection of the hippocampus. , 1966, Brain : a journal of neurology.

[20]  C. Sahley,et al.  8 – Functional Development of the Prefrontal System* , 1984 .

[21]  A. Hjorth-Simonsen,et al.  Origin and termination of the hippocampal perforant path in the rat studied by silver impregnation , 1972, The Journal of comparative neurology.

[22]  A. Scheibel,et al.  A neurohistological correlate of schizophrenia. , 1984, Biological psychiatry.

[23]  S. Mednick,et al.  Perinatal Complications and Clinical Outcome within the Schizophrenia Spectrum , 1982, British Journal of Psychiatry.

[24]  B. Seltzer,et al.  A direct inferior parietal lobule projection to the presubiculum in the rhesus monkey , 1979, Brain Research.

[25]  P. Goldman-Rakic,et al.  Dual pathways connecting the dorsolateral prefrontal cortex with the hippocampal formation and parahippocampal cortex in the rhesus monkey , 1984, Neuroscience.

[26]  V. B. Domesick Projections from the cingulate cortex in the rat. , 1969, Brain research.

[27]  C. Brooks Studies on the Cerebral Cortex , 1933 .

[28]  R Jagoe,et al.  Postmortem evidence of structural brain changes in schizophrenia. Differences in brain weight, temporal horn area, and parahippocampal gyrus compared with affective disorder. , 1986, Archives of general psychiatry.

[29]  Deepak N. Pandya,et al.  Some connections of the entorhinal (area 28) and perirhinal (area 35) cortices of the rhesus monkey. III. Efferent connections , 1975, Brain Research.

[30]  Michael W. Miller,et al.  Cortical connections between rat cingulate cortex and visual, motor, and postsubicular cortices , 1983, The Journal of comparative neurology.