Please use this identifier to cite or link to this item: doi:10.22028/D291-35594
Title: Methylxanthines Induce a Change in the AD/Neurodegeneration-Linked Lipid Profile in Neuroblastoma Cells
Author(s): Janitschke, Daniel
Lauer, Anna Andrea
Bachmann, Cornel Manuel
Winkler, Jakob
Griebsch, Lea Victoria
Pilz, Sabrina Melanie
Theiss, Elena Leoni
Grimm, Heike Sabine
Hartmann, Tobias
Grimm, Marcus Otto Walter
Language: English
Title: International Journal of Molecular Sciences
Volume: 23
Issue: 4
Publisher/Platform: MDPI
Year of Publication: 2022
Free key words: lipidomics
methylxanthines
caffeine
theobromine
theophylline
pentoxifylline
propentofylline
sphingomyelin
ceramide
phosphatidylcholine
plasmalogens
DDC notations: 610 Medicine and health
Publikation type: Journal Article
Abstract: Alzheimer’s disease (AD) is characterized by an increased plaque burden and tangle accumulation in the brain accompanied by extensive lipid alterations. Methylxanthines (MTXs) are alkaloids frequently consumed by dietary intake known to interfere with the molecular mechanisms leading to AD. Besides the fact that MTX consumption is associated with changes in triglycerides and cholesterol in serum and liver, little is known about the effect of MTXs on other lipid classes, which raises the question of whether MTX can alter lipids in a way that may be relevant in AD. Here we have analyzed naturally occurring MTXs caffeine, theobromine, theophylline, and the synthetic MTXs pentoxifylline and propentofylline also used as drugs in different neuroblastoma cell lines. Our results show that lipid alterations are not limited to triglycerides and cholesterol in the liver and serum, but also include changes in sphingomyelins, ceramides, phosphatidylcholine, and plasmalogens in neuroblastoma cells. These changes comprise alterations known to be beneficial, but also adverse effects regarding AD were observed. Our results give an additional perspective of the complex link between MTX and AD, and suggest combining MTX with a lipid-altering diet compensating the adverse effects of MTX rather than using MTX alone to prevent or treat AD.
DOI of the first publication: 10.3390/ijms23042295
Link to this record: urn:nbn:de:bsz:291--ds-355949
hdl:20.500.11880/32504
http://dx.doi.org/10.22028/D291-35594
ISSN: 1422-0067
Date of registration: 1-Mar-2022
Description of the related object: Supplementary Materials
Related object: https://www.mdpi.com/1422-0067/23/4/2295/s1
Faculty: M - Medizinische Fakultät
Department: M - Neurologie und Psychiatrie
Professorship: M - Prof. Dr. Tobias Hartmann
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

Files for this record:
File Description SizeFormat 
ijms-23-02295-v2.pdf3,03 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons