Optimization of mass spectrometry settings for steroidomic analysis in young and old killifish.


Journal

Analytical and bioanalytical chemistry
ISSN: 1618-2650
Titre abrégé: Anal Bioanal Chem
Pays: Germany
ID NLM: 101134327

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 27 01 2020
accepted: 03 04 2020
revised: 02 03 2020
pubmed: 26 4 2020
medline: 4 2 2021
entrez: 26 4 2020
Statut: ppublish

Résumé

Steroids are essential structural components of cell membranes that organize lipid rafts and modulate membrane fluidity. They can also act as signalling molecules that work through nuclear and G protein-coupled receptors to impact health and disease. Notably, changes in steroid levels have been implicated in metabolic, cardiovascular and neurodegenerative diseases, but how alterations in the steroid pool affect ageing is less well understood. One of the major challenges in steroidomic analysis is the ability to simultaneously detect and distinguish various steroids due to low in vivo concentrations and naturally occurring stereoisomers. Here, we established such a method to study the mass spectrometry behaviour of nine sterols/steroids and related molecules (cholesterol precursors: squalene, lanosterol; sterol metabolites; 7 Dehydrocholesterol, 24, 25 and 27 Hydroxycholesterol; and steroids: progesterone, testosterone, and corticosterone) during ageing in the African turquoise killifish, a new model for studying vertebrate longevity. We find that levels of all tested steroids change significantly with age in multiple tissues, suggesting that specific steroids could be used as biomarkers of ageing. These findings pave the way for use of Nothobranchius furzeri as a novel model organism to unravel the role of sterols/steroids in ageing and age-related diseases. Graphical abstract.

Identifiants

pubmed: 32333075
doi: 10.1007/s00216-020-02640-6
pii: 10.1007/s00216-020-02640-6
pmc: PMC7320053
doi:

Substances chimiques

Steroids 0
Cholesterol 97C5T2UQ7J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4089-4099

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Auteurs

Rahel Dabrowski (R)

Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9 b, 50931, Cologne, Germany.

Roberto Ripa (R)

Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9 b, 50931, Cologne, Germany.

Christian Latza (C)

Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9 b, 50931, Cologne, Germany.

Andrea Annibal (A)

Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9 b, 50931, Cologne, Germany. aannibal@age.mpg.de.

Adam Antebi (A)

Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9 b, 50931, Cologne, Germany. aantebi@age.mpg.de.
Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Josef-Stelzmann-Strasse 26, 50931, Cologne, Germany. aantebi@age.mpg.de.

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Classifications MeSH