HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

DHA-PC and PSD-95 decrease after loss of synaptophysin and before neuronal loss in patients with Alzheimer's disease.

Abstract
Alzheimer's disease (AD) is a progressive neurodegenerative disease that is characterized by senile plaques, neurofibrillary tangles, synaptic disruption, and neuronal loss. Several studies have demonstrated decreases of docosahexaenoic acid-containing phosphatidylcholines (DHA-PCs) in the AD brain. In this study, we used matrix-assisted laser desorption/ionization imaging mass spectrometry in postmortem AD brain to show that PC molecular species containing stearate and DHA, namely PC(18:0/22:6), was selectively depleted in the gray matter of patients with AD. Moreover, in the brain regions with marked amyloid β (Aβ) deposition, the magnitude of the PC(18:0/22:6) reduction significantly correlated with disease duration. Furthermore, at the molecular level, this depletion was associated with reduced levels of the postsynaptic protein PSD-95 but not the presynaptic protein synaptophysin. Interestingly, this reduction in PC(18:0/22:6) levels did not correlate with the degrees of Aβ deposition and neuronal loss in AD. The analysis of the correlations of key factors and disease duration showed that their effects on the disease time course were arranged in order as Aβ deposition, presynaptic disruption, postsynaptic disruption coupled with PC(18:0/22:6) reduction, and neuronal loss.
AuthorsDai Yuki, Yuki Sugiura, Nobuhiro Zaima, Hiroyasu Akatsu, Shiro Takei, Ikuko Yao, Masato Maesako, Ayae Kinoshita, Takayuki Yamamoto, Ryo Kon, Keikichi Sugiyama, Mitsutoshi Setou
JournalScientific reports (Sci Rep) Vol. 4 Pg. 7130 (Nov 20 2014) ISSN: 2045-2322 [Electronic] England
PMID25410733 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Amyloid beta-Peptides
  • DLG4 protein, human
  • Disks Large Homolog 4 Protein
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Phosphatidylcholines
  • SYP protein, human
  • Synaptophysin
  • Docosahexaenoic Acids
Topics
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease (genetics, metabolism, pathology)
  • Amyloid beta-Peptides (chemistry, genetics, metabolism)
  • Autopsy
  • Brain Chemistry
  • Cell Death
  • Disease Progression
  • Disks Large Homolog 4 Protein
  • Docosahexaenoic Acids (chemistry, metabolism)
  • Female
  • Gene Expression
  • Gray Matter (chemistry, metabolism, pathology)
  • Humans
  • Intracellular Signaling Peptides and Proteins (genetics, metabolism)
  • Male
  • Membrane Proteins (genetics, metabolism)
  • Neurons (metabolism, pathology)
  • Phosphatidylcholines (chemistry, metabolism)
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Synapses (chemistry, metabolism, pathology)
  • Synaptophysin (genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: