On the structure of the human striate area
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Bibliographic Information
On the structure of the human striate area
（Advances in anatomy, embryology and cell biology, 77）
Springer-Verlag, 1982
- : gw
- : us
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Originally presented as the author's thesis in 1978 (doctoral--Anatomischen Institut, Christian-Albrecht-Universität, Kiel) under title: Habilitationschrift : Licht- und elektronenmikroskopische Untersuchungen zur Morphologie der primären Sehrinde des Menschen
Bibliography: p. 78-86
Includes index
Description and Table of Contents
Description
Primary cortical areas receive a defmed input which makes them especially appropria- te for investigating cortical functions. The striate area is the only isocortical field which can be delineated unequivocally in the human brain. Nevertheless, there have been only a few morphological studies of this particular area (cytoarchitectonic studies: Bailey and Von Bonin 1951, Beck 1934, Von Economo and Koskinas 1925, Filimo- noff 1932; myeloarchitectonic studies: Sanides and Vitzthum 1965, Vogt and Vogt 1919; pigmentoarchitectonic studies: Braak H 1976, 1977). For Golgi impregnations, Ramon y Cajal (1900, 1909-1911), Conel (1939-1967), and Shkol'nik-Yarros (1971) preferred the incompletely myelinated material taken from brains of young childre- a fact that somewhat restricts their descriptions of the human striate area. Pigment preparations (Braak H 1978) provide a detailed view of the lamination of cortical areas. Furthermore, many types of cortical nerve cells reveal a typicallipofus- cin-pigment pattern (Braak H 1974a).
Thus, a correlation can be drawn between the type of neuron as classified in Golgi preparations and the characteristic number and distribution of lipofuscin granules found in the cell body. Neurolipofuscin granules can therefore be considered the internal markers. In this study several cell types of the striate area have been identified under light and electron microscopes by means of their characteristic pigmentation.
Table of Contents
1 Introduction.- 2 Material and Methods.- 3 Lamination Pattern.- 4 Neurons and Neuropil of Layer I.- 4.1 Nissl-Stained and Methylene Blue-Azure II-Stained Sections.- 4.2 Golgi Preparations.- 4.3 Electron Microscopy.- 5 General Remarks Concerning Pyramidal and Nonpyramidal or Stellate Cells.- 5.1 Nissl Preparations.- 5.2 Golgi Preparations.- 5.3 Electron Microscopy.- 6 Pyramidal Cells and Neuropil of Layer II.- 6.1 Nissl Preparations.- 6.2 Golgi Preparations.- 6.3 Electron Microscopy.- 7 Pyramidal Cells and Neuropil of Layer IIIab.- 7.1 Nissl Preparations.- 7.2 Golgi Preparations.- 7.3 Electron Microscopy.- 8 Pyramidal and Polygonal Neurons and Neuropil of Layers IIIc/IVa, IVb, IVc?, and IVc?.- 8.1 General Remarks.- 8.2 Nissl Preparations.- 8.3 Golgi Preparations.- 8.4 Electron Microscopy.- 8.5 Are the Polygonal Neurons Modified Pyramidal Neurons?.- 9 Pyramidal and Polygonal Neurons and Neuropil of Layers IVd/Va and Vb.- 9.1 Nissl-Stained and Methylene Blue-Azure II-Stained Sections.- 9.2 Golgi Preparations.- 9.3 Electron Microscopy.- 10 Pyramidal Cells and Multiformed Neurons of Layers VIa and VIb.- 10.1 Nissl Preparations.- 10.2 Golgi Preparations.- 10.3 Electron Microscopy.- 11 Nonpyramidal Cells of Layers II to VI.- 11.1 Golgi Preparations.- 11.2 Nissl Preparations.- 11.3 Electron Microscopy.- 12 Glial Cells of Layers I to VI.- 12.1 Astrocytes.- 12.2 Oligodendrocytes.- 12.3 Microglial Cells.- 13 Summary.- Acknowledgments.- References.
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