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Choline acetyltransferase and somatostatin levels in aged Microcebus murinus brain

P Dournaud1, J P Gautron, E Pattou

  • 1INSERM U159, Centre Paul Broca, Paris, France.

Neurobiology of Aging
|November 1, 1994
PubMed

Insights

Aging Microcebus murinus brains show beta-amyloid deposits. Choline acetyltransferase activity increased with age, but somatostatin levels remained unchanged, unlike in Alzheimer's disease.

Area of Science:

  • Neuroscience
  • Aging Research
  • Comparative Pathology

Background:

  • Alzheimer's disease (AD) is characterized by beta-amyloid (beta-AP) deposits, decreased choline acetyltransferase (ChAT) activity, and reduced somatostatin (SRIH) levels.
  • Aging Microcebus murinus primates exhibit beta-AP deposits in the brain, similar to AD pathology.

Purpose of the Study:

  • To investigate age-related changes in ChAT activity and SRIH content in the cerebral cortex of Microcebus murinus.
  • To determine if these neurochemical changes correlate with the presence of beta-AP deposits.

Main Methods:

  • Analysis of ChAT activity and SRIH content in the cerebral cortex of middle-aged to aged Microcebus murinus.
  • High-performance liquid chromatography (HPLC) to characterize SRIH immunoreactivity.
  • Histopathological examination for beta-amyloid deposits and cortical lesions.

Main Results:

  • A positive correlation was found between age and ChAT activity.
  • Cortical SRIH content was not significantly affected by age, with four immunoreactive peaks identified, including SRIH-28 and SRIH-14.
  • Amyloid angiopathy was prevalent in all examined brains; however, significant alterations in ChAT activity and SRIH levels were not observed even in the oldest cases with plaque-like lesions.

Conclusions:

  • Aging Microcebus murinus display beta-AP deposition but lack the characteristic decrease in ChAT activity and SRIH content seen in Alzheimer's disease.
  • These findings suggest that beta-AP deposition in aging primates may not directly parallel the neurochemical deficits associated with human Alzheimer's disease.

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