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Cholinergic fiber aberrations in nucleus basalis lesioned rat and Alzheimer's disease

  • R. P.A. Gaykema
  • , C. Nyakas
  • , E. Horvath
  • , L. B. Hersh
  • , C. Majtenyi
  • , P. G.M. Luiten

Producción científica: Articlerevisión exhaustiva

45 Citas (Scopus)

Resumen

-Innervation density and morphological aberrations of cholinergic fibers were studied with choline acetyltransferase (ChAT) immunocytochemistry and acetylcholinesterase (AChE) histochemistry in 30-35 month-old aged rats and rats with long-term bilateral lesions of the magnocellular basal nucleus (MBN). In addition, AChE histochemistry was performed on human cortical sections derived from autopsy brains of normal aged and Alzheimer's disease (AD) patients. A limited but variable number of morphological alterations were observed in ChAT-immunoreactive fibers in the cortex and the hippocampus of the aged control rats. The aged MBN-lesioned rats displayed a severely reduced number of cholinergic fibers in the denervated areas of the neocortex, whereas the surviving fibers showed a strongly increased number of aberrations. Fiber anomalies were also observed in the cortex of the aged human subjects and Alzheimer patients, the latter showing a higher incidence of such aberrations. Only a part of these distended profiles were seen in close association with senile plaques as detected in the AChE-stained material. These findings suggest that experimental MBN lesions combined with aging share with AD the induction of large quantities of fiber malformations. Implications of possible mechanisms in both conditions are discussed.

Idioma originalEnglish
Páginas (desde-hasta)441-448
Número de páginas8
PublicaciónNeurobiology of Aging
Volumen13
N.º3
DOI
EstadoPublished - 1992

Nota bibliográfica

Funding Information:
We thank Jan Gaasnt d Willeke vaRno onf or their skillful assis-tanceH. ansJ. A. Beldhuiiss acknowledged for his heclopmfuml ents on statistical evaluaTtihoins.r esearcwha sp artially supported by the NIH grants AG058a9n3d A G08013to L.B . Hersh.

Financiación

We thank Jan Gaasnt d Willeke vaRno onf or their skillful assis-tanceH. ansJ. A. Beldhuiiss acknowledged for his heclopmfuml ents on statistical evaluaTtihoins.r esearcwha sp artially supported by the NIH grants AG058a9n3d A G08013to L.B . Hersh.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
National Institute on AgingR01AG005893

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • General Neuroscience
    • Aging
    • Clinical Neurology
    • Developmental Biology
    • Geriatrics and Gerontology

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