THE QUANTITATIVE HISTOCHEMISTRY OF THE CEREBRAL CORTEX—I. ARCHITECTONIC DISTRIBUTION OF TEN CHEMICAL CONSTITUENTS IN THE MOTOR AND VISUAL CORTICES *

THE development of quantitative methods for the measurement of chemical and enzymatic tissue constituents in samples of tissue weighing less than 10 p g has made possible the study of the amount and localization of these constituents at rather precise locations in the brain (ROBINS and SMITH, 1953; LOWRY, ROBERTS, LEINER, Wu, FARR, and ALBERS, 1954; POPE, 1952). By utilization of these methods, it is possible to study the chemical and enzymatic architectonics of the cerebral cortex. In this report, the results of a study of the distribution of dry weight per unit volume, protein, total lipide, cephalins, lecithins, sphingomyelins, total sphingolipides. non-phosphorus-containing sphingolipides, total phospholipides, cholesterol, and number of cells per unit volume in each histologically defined layer and sublayer of the motor cortex and visual cortex of the monkey are presented. In thc accompanying papers, studies of some of the enzymatic constituents of these layers ( R O B I ~ S , MITH, EYDT, and MCCAMAN, 1956) and of analyses at 50 p intervals compared with those by architectonic layers throughout the depth of the two cortices (ROBINS. MITH, and EYDT, 1956) are reported.

[1]  D. E. Smith,et al.  Distribution of lipides in the cerebellar cortex and its subjacent white matter. , 1956, The Journal of biological chemistry.

[2]  E. Robins,et al.  Microdetermination of phospholipides and sphingolipides in brain. , 1956, The Journal of biological chemistry.

[3]  D. E. Smith,et al.  THE QUANTITATIVE HISTOCHEMISTRY OF THE CEREBRAL CORTEX—II. ARCHITECTONIC DISTRIBUTION OF NINE ENZYMES IN THE MOTOR AND VISUAL CORTICES * , 1956, Journal of neurochemistry.

[4]  E. Robins,et al.  THE QUANTITATIVE HISTOCHEMISTRY OF THE CEREBRAL CORTEX—III. ANALYSES AT 50 μ INTERVALS COMPARED WITH ANALYSES BY ARCHITECTONIC LAYERS IN THE MOTOR AND VISUAL CORTICES * , 1956, Journal of neurochemistry.

[5]  B. Glass Biochemistry of the Developing Nervous System , 1956 .

[6]  O. H. Lowry,et al.  Fluorometric Determination of 0.1 to 10 Micrograms of Cholesterol , 1955 .

[7]  K. Elliott,et al.  Desoxyribonucleic acid content and cell density in brain and human brain tumors. , 1954, Canadian journal of biochemistry and physiology.

[8]  O. H. Lowry,et al.  The quantitative histochemistry of brain. I. Chemical methods. , 1954, The Journal of biological chemistry.

[9]  O. H. Lowry,et al.  The quantitative histochemistry of brain. III. Ammon's horn. , 1954, The Journal of biological chemistry.

[10]  G. A. Shariff,et al.  Cell counts in the primate cerebral cortex , 1953, The Journal of comparative neurology.

[11]  R. Rossiter,et al.  Estimation of nucleic acids in tissue from the nervous system. , 1952, The Biochemical journal.

[12]  A. Pope Quantitative distribution of dipeptidase and acetylcholine esterase in architectonic layers of rat cerebral cortex. , 1952, Journal of neurophysiology.

[13]  Oliver H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[14]  F. Mettler,et al.  Cell concentration and laminar thickness in the frontal cortex of psychotic patients; studies on cortex removed at operation , 1949, The Journal of comparative neurology.

[15]  P. Bucy The Precentral Motor Cortex , 1946 .

[16]  G. Bonin,et al.  The striate area of primates , 1942 .

[17]  J. O'leary,et al.  Structure of the area striata of the cat , 1941 .

[18]  A. Johnson,et al.  Lipids of normal brain. , 1948, The Biochemical journal.

[19]  R. Stowell Effect on Tissue Volume of Various Methods of Fixation, Dehydration, and Embedding , 1941 .