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Subpopulations of mesencephalic dopaminergic neurons express different levels of tyrosine hydroxylase messenger RNA
Author(s) -
WeissWunder Linda T.,
Chesselet MarieFrançloise
Publication year - 1991
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.903030312
Subject(s) - pars compacta , substantia nigra , tyrosine hydroxylase , ventral tegmental area , biology , dopamine , dopaminergic , midbrain , tyrosine 3 monooxygenase , neuroscience , medicine , endocrinology , microbiology and biotechnology , central nervous system
Subpopulations of mesencephalic dopamine containing neurons possess different electro‐physiological, pharmacological, biochemical, and anatomical properties. In order to determine whether such differences are related to the regulation of tyrosine hydroxylase, the rate limiting enzyme in the synthesis of catecholamines, the regional distribution of tyrosine hydroxylase messenger RNA in these neurons was examined using in situ hybridization histochemistry. In the mouse, labelling for tyrosine hydroxylase messenger RNA associated with individual neurons was significantly less in the lateral substantia nigra pars compacta than in the medial substantia nigra pars compacta and the ventral tegmental area. A similar pattern of labelling was observed in the rat. Labelling for tyrosine hydroxylase messenger RNA was significantly less in the lateral substantia nigra pars compacta than in medial pars compacta (a densely cellular region), the area dorsal to the medial substantia nigra pars compacta (a less cell dense region), and the ventral tegmental area. Differences in levels of labelling for messenger RNA in mesencephalic dopamine neurons were not related to differences in cell size as measured in sections processed for tyrosine hydroxylase immunohistochemistry. The results suggest that tyrosine hydroxylase messenger RNA is differentially regulated in Subpopulations of mesencephalic dopamine neurons, supporting the view that these neurons are physiologically distinct.

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