[De novo biosynthesis of glycerophospholipids and longevity].

Biosíntesis de novo de glicerofosfolípidos y longevidad.
Diacilglicéridos Diacylglycerides Espectrometría de masas Lipidomics Lipidómica Longevidad máxima Mass spectrometry Maximum longevity

Journal

Revista espanola de geriatria y gerontologia
ISSN: 1578-1747
Titre abrégé: Rev Esp Geriatr Gerontol
Pays: Spain
ID NLM: 8009022

Informations de publication

Date de publication:
Historique:
received: 01 03 2018
revised: 30 05 2018
accepted: 31 05 2018
entrez: 19 3 2019
pubmed: 19 3 2019
medline: 8 5 2020
Statut: ppublish

Résumé

The glycerophospholipids, synthesised from diacylglycerol (DAG), are one of the main lipid components of cell membranes. The lipid profile is an optimised feature associated with animal longevity. In this context, the hypothesis is presented that the DAG biosynthesis rate, and thus, the glycerophospholipids content, is related to animal longevity. A plasma lipidomic analysis was performed based on the mass spectrometry of 11 mammalian species with a maximum longevity ranging from 3.5 to 120 years. Lipid identification was based on exact mass, retention time, and isotopic distribution. ANOVA test was applied to differentiate the lipids between animal species. The relationship between these lipids and longevity was carried out with a Spearman correlation. Data was analysed using SPSS and MetaboAnalyst. Among the 1,061 different lipid molecular species found between species, 47 were defined as DAG. Interestingly, 14 of them showed a negative correlation with mammalian maximum longevity. Multivariate statistics revealed that 14 DAGs were enough to define mammalian species and their maximum longevity. Data suggest that long-lived mammalian species have a lower rate of glycerophospholipids synthesis through the de novo pathway, possibly associated with a lower rate of membrane lipid exchange, which in turn is related to lower energy expenditure.

Sections du résumé

BACKGROUND BACKGROUND
The glycerophospholipids, synthesised from diacylglycerol (DAG), are one of the main lipid components of cell membranes. The lipid profile is an optimised feature associated with animal longevity. In this context, the hypothesis is presented that the DAG biosynthesis rate, and thus, the glycerophospholipids content, is related to animal longevity.
MATERIAL AND METHODS METHODS
A plasma lipidomic analysis was performed based on the mass spectrometry of 11 mammalian species with a maximum longevity ranging from 3.5 to 120 years. Lipid identification was based on exact mass, retention time, and isotopic distribution. ANOVA test was applied to differentiate the lipids between animal species. The relationship between these lipids and longevity was carried out with a Spearman correlation. Data was analysed using SPSS and MetaboAnalyst.
RESULTS RESULTS
Among the 1,061 different lipid molecular species found between species, 47 were defined as DAG. Interestingly, 14 of them showed a negative correlation with mammalian maximum longevity. Multivariate statistics revealed that 14 DAGs were enough to define mammalian species and their maximum longevity.
CONCLUSIONS CONCLUSIONS
Data suggest that long-lived mammalian species have a lower rate of glycerophospholipids synthesis through the de novo pathway, possibly associated with a lower rate of membrane lipid exchange, which in turn is related to lower energy expenditure.

Identifiants

pubmed: 30879491
pii: S0211-139X(18)30580-8
doi: 10.1016/j.regg.2018.05.006
pii:
doi:

Substances chimiques

Glycerophospholipids 0

Types de publication

Journal Article

Langues

spa

Sous-ensembles de citation

IM

Pagination

88-93

Informations de copyright

Copyright © 2018 SEGG. Publicado por Elsevier España, S.L.U. All rights reserved.

Auteurs

Natalia Mota-Martorell (N)

Departament de Medicina Experimental, Universitat de Lleida-Institut de Recerca Biomèdica de Lleida (UdL-IRBLleida), Lleida, España.

Irene Pradas (I)

Departament de Medicina Experimental, Universitat de Lleida-Institut de Recerca Biomèdica de Lleida (UdL-IRBLleida), Lleida, España.

Mariona Jové (M)

Departament de Medicina Experimental, Universitat de Lleida-Institut de Recerca Biomèdica de Lleida (UdL-IRBLleida), Lleida, España.

Alba Naudí (A)

Departament de Medicina Experimental, Universitat de Lleida-Institut de Recerca Biomèdica de Lleida (UdL-IRBLleida), Lleida, España.

Reinald Pamplona (R)

Departament de Medicina Experimental, Universitat de Lleida-Institut de Recerca Biomèdica de Lleida (UdL-IRBLleida), Lleida, España. Electronic address: reinald.pamplona@mex.udl.cat.

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Classifications MeSH