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Quantitative Maps of GAbAergic and Glutamatergic Neuronal Systems in the Human Brain

Overview
Journal Hum Brain Mapp
Publisher Wiley
Specialty Neurology
Date 2000 Nov 4
PMID 11061336
Citations 8
Authors
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Abstract

GABAergic and glutamatergic neuronal systems in adult normal human brains were shown quantitatively and in detail through the distributions of glutamate decarboxylase (GAD) and glutamate dehydrogenase (GDH), respectively. Consecutive coronal sections containing part of the striatum and the substantia nigra were obtained from the right hemisphere of three deceased persons with no history of neurological or psychiatric diseases and were stained immunohistochemically for GAD and GDH. Each stained section was divided into approximately 3 million microareas and the immunohistochemical fluorescence intensity in each area was measured by a human brain mapping analyzer, which is a microphotometry system for analysis of the distribution of neurochemicals in a large tissue slice. In the analyzed brain regions, conspicuously intense GAD-like immunoreactivity was observed in the substantia nigra, globus pallidus, and hypothalamus. GDH was widely and rather evenly distributed in the gray matter compared to GAD, although intense GDH-like immunoreactivity was observed in the lateral geniculate nucleus and substantia nigra. Within the substantia nigra, the globus pallidus, and other regions, characteristic distributions of GAD- and GDH-like immunoreactivity were found. We believe that the analysis of the human brain by this novel technique can help to understand the functional distribution of neuronal systems in the normal human brain and may be able to identify abnormal changes in the diseased human brain. It can also provide basic data to help in the interpretation of functional magnetic resonance imaging or positron emission tomography.

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References
1.
Sutoo D, Akiyama K, Maeda I . [The development of a high sensitivity and high linearity fluorescence microphotometry system for distribution analysis of neurotransmitter in the brain]. Nihon Yakurigaku Zasshi. 1988; 91(4):173-80. DOI: 10.1254/fpj.91.173. View

2.
Mesulam M, Geula C . Nucleus basalis (Ch4) and cortical cholinergic innervation in the human brain: observations based on the distribution of acetylcholinesterase and choline acetyltransferase. J Comp Neurol. 1988; 275(2):216-40. DOI: 10.1002/cne.902750205. View

3.
YATES R, Roberts P . Effects of enucleation and intra-ocular colchicine on the amino acids of frog optic tectum. J Neurochem. 1974; 23(4):891-3. DOI: 10.1111/j.1471-4159.1974.tb04423.x. View

4.
Fisher H . L-Glutamate dehydrogenase from bovine liver. Methods Enzymol. 1985; 113:16-27. DOI: 10.1016/s0076-6879(85)13006-5. View

5.
Sutoo D, Akiyama K, Yabe K, Kohno K . Multiple analysis of tyrosine hydroxylase and calmodulin distributions in the forebrain of the rat using a microphotometry system. Brain Res Bull. 1991; 26(6):973-82. DOI: 10.1016/0361-9230(91)90265-l. View