TY - JOUR
T1 - Changes in Liver Lipidomic Profile in G2019S-LRRK2 Mouse Model of Parkinson’s Disease
AU - Corral Nieto, Yaiza
AU - Yakhine-Diop, Sokhna M.S.
AU - Moreno-Cruz, Paula
AU - Manrique García, Laura
AU - Gabrielly Pereira, Amanda
AU - Morales-García, José A.
AU - Niso-Santano, Mireia
AU - González-Polo, Rosa A.
AU - Uribe-Carretero, Elisabet
AU - Durand, Sylvère
AU - Maiuri, Maria Chiara
AU - Paredes-Barquero, Marta
AU - Alegre-Cortés, Eva
AU - Canales-Cortés, Saray
AU - López de Munain, Adolfo
AU - Pérez-Tur, Jordi
AU - Pérez-Castillo, Ana
AU - Kroemer, Guido
AU - Fuentes, José M.
AU - Bravo-San Pedro, José M.
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/3/1
Y1 - 2023/3/1
N2 - The identification of Parkinson’s disease (PD) biomarkers has become a main goal for the diagnosis of this neurodegenerative disorder. PD has not only been intrinsically related to neurological problems, but also to a series of alterations in peripheral metabolism. The purpose of this study was to identify metabolic changes in the liver in mouse models of PD with the scope of finding new peripheral biomarkers for PD diagnosis. To achieve this goal, we used mass spectrometry technology to determine the complete metabolomic profile of liver and striatal tissue samples from WT mice, 6-hydroxydopamine-treated mice (idiopathic model) and mice affected by the G2019S-LRRK2 mutation in LRRK2/PARK8 gene (genetic model). This analysis revealed that the metabolism of carbohydrates, nucleotides and nucleosides was similarly altered in the liver from the two PD mouse models. However, long-chain fatty acids, phosphatidylcholine and other related lipid metabolites were only altered in hepatocytes from G2019S-LRRK2 mice. In summary, these results reveal specific differences, mainly in lipid metabolism, between idiopathic and genetic PD models in peripheral tissues and open up new possibilities to better understand the etiology of this neurological disorder.
AB - The identification of Parkinson’s disease (PD) biomarkers has become a main goal for the diagnosis of this neurodegenerative disorder. PD has not only been intrinsically related to neurological problems, but also to a series of alterations in peripheral metabolism. The purpose of this study was to identify metabolic changes in the liver in mouse models of PD with the scope of finding new peripheral biomarkers for PD diagnosis. To achieve this goal, we used mass spectrometry technology to determine the complete metabolomic profile of liver and striatal tissue samples from WT mice, 6-hydroxydopamine-treated mice (idiopathic model) and mice affected by the G2019S-LRRK2 mutation in LRRK2/PARK8 gene (genetic model). This analysis revealed that the metabolism of carbohydrates, nucleotides and nucleosides was similarly altered in the liver from the two PD mouse models. However, long-chain fatty acids, phosphatidylcholine and other related lipid metabolites were only altered in hepatocytes from G2019S-LRRK2 mice. In summary, these results reveal specific differences, mainly in lipid metabolism, between idiopathic and genetic PD models in peripheral tissues and open up new possibilities to better understand the etiology of this neurological disorder.
KW - lipids
KW - liver
KW - LRRK2
KW - metabolome
KW - neurodegeneration
KW - Parkinson
UR - http://www.scopus.com/inward/record.url?scp=85149712000&partnerID=8YFLogxK
U2 - 10.3390/cells12050806
DO - 10.3390/cells12050806
M3 - Article
C2 - 36899942
AN - SCOPUS:85149712000
SN - 2073-4409
VL - 12
JO - Cells
JF - Cells
IS - 5
M1 - 806
ER -