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Exp Neurol ; 193(2): 444-54, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15869947

ABSTRACT

The present study examined in the rat the effect of a partial lesion of the nigrostriatal dopaminergic pathway induced by intrastriatal injection of 6-hydroxydopamine (6-OHDA), on the dopaminergic innervation of the cortex and the globus pallidus as revealed using tyrosine hydroxylase (TH) immunoreactivity. Twenty-eight days after unilateral injection of 6-OHDA into the dorsal part of the striatum, TH-positive fiber density was reduced by 41% in the dorsal and central part of the structure, and was accompanied by a retrograde loss of 33% of TH-positive neurons in the substantia nigra (SN), while the ventral tegmental area was completely spared. In the SN, TH-positive cell loss was most severe in the ventral part of the structure (-55%). In the same animals, a substantial loss of TH-positive fibers was evident in the dorsal part of the globus pallidus, and involved both thick fibers of passage and thin varicose terminal axonal branches. In the cortex, a loss of TH-positive fibers was prominent in the cingulate area, moderate in the motor area and less affected in the insular area, while the noradrenergic innervation revealed using dopamine-beta-hydroxylase immunoreactivity was preserved in all of these cortical subregions. These results demonstrate that the intrastriatal 6-OHDA lesion model in rats produces a significant loss of dopaminergic axons in extrastriatal structures including the pallidum and cortex, which may contribute to functional sequelae in this animal model of Parkinson's disease.


Subject(s)
Adrenergic Agents/toxicity , Cerebral Cortex/metabolism , Dopamine/metabolism , Globus Pallidus/metabolism , Oxidopamine/toxicity , Substantia Nigra/drug effects , Animals , Cell Count/methods , Functional Laterality/physiology , Immunohistochemistry/methods , Male , Nerve Fibers/metabolism , Neural Pathways/metabolism , Rats , Rats, Sprague-Dawley , Substantia Nigra/injuries , Substantia Nigra/pathology , Tyrosine 3-Monooxygenase/metabolism
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