Effects of lifestyle intervention in tissue‐specific lipidomic profile of formerly obese mice
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Effects of lifestyle intervention in tissue‐specific lipidomic profile of formerly obese mice. / Dahdah, Norma; Gonzalez‐franquesa, Alba; Samino, Sara; Gama‐perez, Pau; Herrero, Laura; Perales, José Carlos; Yanes, Oscar; Malagón, Maria Del Mar; Garcia‐roves, Pablo Miguel.
In: International Journal of Molecular Sciences, Vol. 22, No. 7, 3694, 2021.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Effects of lifestyle intervention in tissue‐specific lipidomic profile of formerly obese mice
AU - Dahdah, Norma
AU - Gonzalez‐franquesa, Alba
AU - Samino, Sara
AU - Gama‐perez, Pau
AU - Herrero, Laura
AU - Perales, José Carlos
AU - Yanes, Oscar
AU - Malagón, Maria Del Mar
AU - Garcia‐roves, Pablo Miguel
PY - 2021
Y1 - 2021
N2 - Lipids are highly diverse in their composition, properties and distribution in different biological entities. We aim to establish the lipidomes of several insulin‐sensitive tissues and to test their plasticity when divergent feeding regimens and lifestyles are imposed. Here, we report a pro-ton nuclear magnetic resonance (1H‐NMR) study of lipid abundance across 4 tissues of C57Bl6J male mice that includes the changes in the lipid profile after every lifestyle intervention. Every tissue analysed presented a specific lipid profile irrespective of interventions. Glycerolipids and fatty acids were most abundant in epididymal white adipose tissue (eWAT) followed by liver, whereas sterol lipids and phosphoglycerolipids were highly enriched in hypothalamus, and gastrocnemius had the lowest content in all lipid species compared to the other tissues. Both when subjected to a high-fat diet (HFD) and after a subsequent lifestyle intervention (INT), the lipidome of hypothalamus showed no changes. Gastrocnemius and liver revealed a pattern of increase in content in many lipid species after HFD followed by a regression to basal levels after INT, while eWAT lipidome was affected mainly by the fat composition of the administered diets and not their caloric density. Thus, the present study demonstrates a unique lipidome for each tissue modulated by caloric intake and dietary composition.
AB - Lipids are highly diverse in their composition, properties and distribution in different biological entities. We aim to establish the lipidomes of several insulin‐sensitive tissues and to test their plasticity when divergent feeding regimens and lifestyles are imposed. Here, we report a pro-ton nuclear magnetic resonance (1H‐NMR) study of lipid abundance across 4 tissues of C57Bl6J male mice that includes the changes in the lipid profile after every lifestyle intervention. Every tissue analysed presented a specific lipid profile irrespective of interventions. Glycerolipids and fatty acids were most abundant in epididymal white adipose tissue (eWAT) followed by liver, whereas sterol lipids and phosphoglycerolipids were highly enriched in hypothalamus, and gastrocnemius had the lowest content in all lipid species compared to the other tissues. Both when subjected to a high-fat diet (HFD) and after a subsequent lifestyle intervention (INT), the lipidome of hypothalamus showed no changes. Gastrocnemius and liver revealed a pattern of increase in content in many lipid species after HFD followed by a regression to basal levels after INT, while eWAT lipidome was affected mainly by the fat composition of the administered diets and not their caloric density. Thus, the present study demonstrates a unique lipidome for each tissue modulated by caloric intake and dietary composition.
KW - Diet composition
KW - Energy intake
KW - Exercise
KW - Gastrocnemius
KW - Hypo-thalamus
KW - Lipidomics
KW - Liver
KW - Plasticity
KW - Tissue‐specific
KW - White adipose tissue
U2 - 10.3390/ijms22073694
DO - 10.3390/ijms22073694
M3 - Journal article
C2 - 33916315
AN - SCOPUS:85103308875
VL - 22
JO - International Journal of Molecular Sciences (CD-ROM)
JF - International Journal of Molecular Sciences (CD-ROM)
SN - 1424-6783
IS - 7
M1 - 3694
ER -
ID: 261002401