Cells (Mar 2023)

Changes in Liver Lipidomic Profile in G2019S-<i>LRRK2</i> Mouse Model of Parkinson’s Disease

  • Yaiza Corral Nieto,
  • Sokhna M. S. Yakhine-Diop,
  • Paula Moreno-Cruz,
  • Laura Manrique García,
  • Amanda Gabrielly Pereira,
  • José A. Morales-García,
  • Mireia Niso-Santano,
  • Rosa A. González-Polo,
  • Elisabet Uribe-Carretero,
  • Sylvère Durand,
  • Maria Chiara Maiuri,
  • Marta Paredes-Barquero,
  • Eva Alegre-Cortés,
  • Saray Canales-Cortés,
  • Adolfo López de Munain,
  • Jordi Pérez-Tur,
  • Ana Pérez-Castillo,
  • Guido Kroemer,
  • José M. Fuentes,
  • José M. Bravo-San Pedro

DOI
https://doi.org/10.3390/cells12050806
Journal volume & issue
Vol. 12, no. 5
p. 806

Abstract

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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.

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