Decreased DHA-containing phospholipids in the neocortex of dementia with Lewy bodies are associated with soluble Aβ
Humans
alpha-Synuclein
/ metabolism
Lewy Body Disease
/ pathology
Neocortex
/ metabolism
Docosahexaenoic Acids
/ metabolism
Chromatography, Liquid
Tandem Mass Spectrometry
Alzheimer Disease
/ pathology
Amyloid beta-Peptides
/ metabolism
Phospholipids
/ metabolism
Fatty Acid-Binding Proteins
/ metabolism
beta-amyloid
dementia with Lewy bodies
docosahexaenoic acid
neocortex
synaptopathology
α-synuclein
Journal
Brain pathology (Zurich, Switzerland)
ISSN: 1750-3639
Titre abrégé: Brain Pathol
Pays: Switzerland
ID NLM: 9216781
Informations de publication
Date de publication:
11 2023
11 2023
Historique:
received:
01
01
2023
accepted:
03
07
2023
medline:
23
10
2023
pubmed:
18
7
2023
entrez:
18
7
2023
Statut:
ppublish
Résumé
Docosahexaenoic acid (DHA) is an essential omega-3 polyunsaturated fatty acid implicated in cognitive functions by promoting synaptic protein expression. While alterations of specific DHA-containing phospholipids have been described in the neocortex of patients with Alzheimer's disease (AD), the status of these lipids in dementia with Lewy bodies (DLB), known to manifest aggregated α-synuclein-containing Lewy bodies together with variable amyloid pathology, is unclear. In this study, post-mortem samples from the parietal cortex of 25 DLB patients and 17 age-matched controls were processed for phospholipidomics analyses using a liquid chromatography-tandem mass spectrometry (LC-MS/MS) platform. After controlling for false discovery rate, six out of the 46 identified putative DHA-phospholipid species were significantly decreased in DLB, with only one showing increase. Altered putative DHA-phospholipid species were subsequently validated with further LC-MS/MS measurements. Of the DHA-containing phospholipid (DCP) species showing decreases, five negatively correlated with soluble beta-amyloid (Aβ42) levels, whilst three also correlated with phosphorylated α-synuclein (all p < 0.05). Furthermore, five of these phospholipid species correlated with deficits of presynaptic Rab3A, postsynaptic neurogranin, or both (all p < 0.05). Finally, we found altered immunoreactivities of brain lysolipid DHA transporter, MFSD2A, and the fatty acid binding protein FABP5 in DLB parietal cortex. In summary, we report alterations of specific DCP species in DLB, as well as their associations with markers of neuropathological burden and synaptopathology. These results support the potential role of DHA perturbations in DLB as well as therapeutic targets.
Identifiants
pubmed: 37463072
doi: 10.1111/bpa.13190
pmc: PMC10580008
doi:
Substances chimiques
alpha-Synuclein
0
Docosahexaenoic Acids
25167-62-8
Amyloid beta-Peptides
0
Phospholipids
0
FABP5 protein, human
0
Fatty Acid-Binding Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e13190Informations de copyright
© 2023 The Authors. Brain Pathology published by John Wiley & Sons Ltd on behalf of International Society of Neuropathology.
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