Preservation of midbrain catecholaminergic neurons in very old human subjects
Identifieur interne : 002313 ( Istex/Curation ); précédent : 002312; suivant : 002314Preservation of midbrain catecholaminergic neurons in very old human subjects
Auteurs : N. Kubis ; B. A. Faucheux ; G. Ransmayr [Autriche] ; P. Damier ; C. Duyckaerts ; D. Henin ; B. Forette ; Y. Le Charpentier [France] ; J.-J. Hauw ; Y. Agid ; E. C. HirschSource :
- Brain [ 0006-8950 ] ; 2000-02.
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Abstract
Parkinson's disease is characterized by a progressive degeneration of dopaminergic neurons in the midbrain, yet the cause of this neuronal loss is still unknown. It has been hypothesized that Parkinson's disease could be the consequence of accelerated ageing. In order to reveal a possible common process during ageing and Parkinson's disease neurodegeneration, catecholaminergic neurons of five anatomical regions of the brainstem (substantia nigra, central grey substance, ventral tegmental area, peri- and retrorubral area, and locus coeruleus) have been quantified using immunohistochemical staining for tyrosine hydroxylase (TH) on regularly spaced sections, between the rostral and caudal poles of the mesencephalon and in the rostral pole of the pons, in post-mortem samples of 21 control subjects who died at ages 44–110 years. No statistically significant loss of TH positive neurons was observed in the older subjects, either in the substantia nigra or in the other midbrain regions that are known to degenerate to a lesser degree in Parkinson's disease. Furthermore, in the later regions no neuronal loss was observed from age 44 to 80 years, indicating that this result is not dependent on the inclusion of `supernormal' very old people. These results suggest that from age 44 to 110 years, ageing in control adults is not, or is scarcely, accompanied by catecholaminergic cell loss in the midbrain and hence Parkinson's disease is probably not caused by an acceleration of a degenerative process during ageing.
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DOI: 10.1093/brain/123.2.366
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N. Kubis<affiliation><mods:affiliation>INSERM U289 and</mods:affiliation><wicri:noCountry code="no comma">INSERM U289 and</wicri:noCountry></affiliation><affiliation><mods:affiliation>INSERM U289 and</mods:affiliation><wicri:noCountry code="no comma">INSERM U289 and</wicri:noCountry></affiliation><affiliation><mods:affiliation>INSERM U289 and</mods:affiliation><wicri:noCountry code="no comma">INSERM U289 and</wicri:noCountry></affiliation><affiliation><mods:affiliation>Laboratoire de Neuropathologie R. Escourolle, INSERM U360, Hôpital de la Salpêtrière,</mods:affiliation><wicri:noCountry code="subField"></wicri:noCountry></affiliation><affiliation><mods:affiliation>Service d'Anatomo-Pathologie, Hôpital Bichat,</mods:affiliation><wicri:noCountry code="subField"></wicri:noCountry></affiliation><affiliation><mods:affiliation>Service de Gériatrie, Hôpital Sainte-Périne,</mods:affiliation><wicri:noCountry code="subField"></wicri:noCountry></affiliation><affiliation><mods:affiliation>Laboratoire de Neuropathologie R. Escourolle, INSERM U360, Hôpital de la Salpêtrière,</mods:affiliation><wicri:noCountry code="subField"></wicri:noCountry></affiliation><affiliation><mods:affiliation>INSERM U289 and</mods:affiliation><wicri:noCountry code="no comma">INSERM U289 and</wicri:noCountry></affiliation><affiliation><mods:affiliation>INSERM U289 and</mods:affiliation><wicri:noCountry code="no comma">INSERM U289 and</wicri:noCountry></affiliation>Le document en format XML
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Kubis</name><affiliation><mods:affiliation>INSERM U289 and</mods:affiliation><wicri:noCountry code="no comma">INSERM U289 and</wicri:noCountry></affiliation></author><author><name sortKey="Faucheux, B A" sort="Faucheux, B A" uniqKey="Faucheux B" first="B. A." last="Faucheux">B. A. Faucheux</name><affiliation><mods:affiliation>INSERM U289 and</mods:affiliation><wicri:noCountry code="no comma">INSERM U289 and</wicri:noCountry></affiliation></author><author><name sortKey="Ransmayr, G" sort="Ransmayr, G" uniqKey="Ransmayr G" first="G." last="Ransmayr">G. Ransmayr</name><affiliation wicri:level="1"><mods:affiliation>Universität Klinik für Neurologie, Innsbrück, Austria</mods:affiliation><country xml:lang="fr">Autriche</country><wicri:regionArea>Universität Klinik für Neurologie, Innsbrück</wicri:regionArea></affiliation></author><author><name sortKey="Damier, P" sort="Damier, P" uniqKey="Damier P" first="P." last="Damier">P. 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Forette</name><affiliation><mods:affiliation>Service de Gériatrie, Hôpital Sainte-Périne,</mods:affiliation><wicri:noCountry code="subField"></wicri:noCountry></affiliation></author><author><name sortKey="Le Charpentier, Y" sort="Le Charpentier, Y" uniqKey="Le Charpentier Y" first="Y." last="Le Charpentier">Y. Le Charpentier</name><affiliation wicri:level="1"><mods:affiliation>Service d'Anatomo-Pathologie, Hôpital de la Pitié, Paris, France and</mods:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Service d'Anatomo-Pathologie, Hôpital de la Pitié, Paris</wicri:regionArea></affiliation></author><author><name sortKey="Hauw, J J" sort="Hauw, J J" uniqKey="Hauw J" first="J.-J." last="Hauw">J.-J. Hauw</name><affiliation><mods:affiliation>Laboratoire de Neuropathologie R. 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Hirsch</name><affiliation><mods:affiliation>INSERM U289 and</mods:affiliation><wicri:noCountry code="no comma">INSERM U289 and</wicri:noCountry></affiliation></author></analytic><monogr></monogr><series><title level="j">Brain</title><title level="j" type="abbrev">Brain</title><idno type="ISSN">0006-8950</idno><idno type="eISSN">1460-2156</idno><imprint><publisher>Oxford University Press</publisher><date type="published" when="2000-02">2000-02</date><biblScope unit="volume">123</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="366">366</biblScope><biblScope unit="page" to="373">373</biblScope></imprint><idno type="ISSN">0006-8950</idno></series><idno type="istex">58AD85E646F93D5D47E891CD8CBB2ED4C4CBF147</idno><idno type="DOI">10.1093/brain/123.2.366</idno><idno type="PII">1460-2156</idno><idno type="local">1230366</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0006-8950</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>A8 = peri- and retro-rubral catecholaminergic cell group A8</term><term>AChE = acetylcholinesterase</term><term>CGS = central grey substance</term><term>LC = locus coeruleus</term><term>SNpc = substantia nigra pars compacta</term><term>TH = tyrosine hydroxylase</term><term>VTA = ventral tegmental area</term><term>ageing</term><term>human</term><term>substantia nigra</term><term>tyrosine hydroxylase</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Parkinson's disease is characterized by a progressive degeneration of dopaminergic neurons in the midbrain, yet the cause of this neuronal loss is still unknown. It has been hypothesized that Parkinson's disease could be the consequence of accelerated ageing. In order to reveal a possible common process during ageing and Parkinson's disease neurodegeneration, catecholaminergic neurons of five anatomical regions of the brainstem (substantia nigra, central grey substance, ventral tegmental area, peri- and retrorubral area, and locus coeruleus) have been quantified using immunohistochemical staining for tyrosine hydroxylase (TH) on regularly spaced sections, between the rostral and caudal poles of the mesencephalon and in the rostral pole of the pons, in post-mortem samples of 21 control subjects who died at ages 44–110 years. No statistically significant loss of TH positive neurons was observed in the older subjects, either in the substantia nigra or in the other midbrain regions that are known to degenerate to a lesser degree in Parkinson's disease. Furthermore, in the later regions no neuronal loss was observed from age 44 to 80 years, indicating that this result is not dependent on the inclusion of `supernormal' very old people. These results suggest that from age 44 to 110 years, ageing in control adults is not, or is scarcely, accompanied by catecholaminergic cell loss in the midbrain and hence Parkinson's disease is probably not caused by an acceleration of a degenerative process during ageing.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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