Sex-specific lipid molecular signatures in obesity-associated metabolic dysfunctions revealed by lipidomic characterization in ob/ob mouse | Biology of Sex Differences | Full Text

Sex-specific lipid molecular signatures in obesity-associated metabolic dysfunctions revealed by lipidomic characterization in ob/ob mouse | Biology of Sex Differences | Full Text

Biology of Sex Differences

Sex-specific lipid molecular signatures in obesity-associated metabolic dysfunctions revealed by lipidomic characterization in ob/ob mouse

• Marcela González-Granillo,
• Luisa A. Helguero†,
• Eliana Alves†,
• Amena Archer,
• Christina Savva,
• Matteo Pedrelli,
• Osman Ahmed,
• Xidan Li,
• Maria Rosário Domingues,
• Paolo Parini,
• Jan-Åke Gustafsson and
• Marion Korach-AndréEmail authorView ORCID ID profile

†Contributed equally

Biology of Sex Differences201910:11

https://doi.org/10.1186/s13293-019-0225-y

©  The Author(s). 2019

• Received: 12 November 2018
• Accepted: 7 February 2019
• Published: 26 February 2019

Abstract

The response to overfeeding is sex dependent, and metabolic syndrome is more likely associated to obesity in men or postmenopausal women than in young fertile women. We hypothesized that obesity-induced metabolic syndrome is sex dependent due to a sex-specific regulation of the fatty acid (FA) synthesis pathways in liver and white adipose depots. We aimed to identify distinctive molecular signatures between sexes using a lipidomics approach to characterize lipid species in liver, perigonadal adipose tissue, and inguinal adipose tissue and correlate them to the physiopathological responses observed. Males had less total fat but lower subcutaneous on visceral fat ratio together with higher liver weight and higher liver and serum triglyceride (TG) levels. Males were insulin resistant compared to females. Fatty acid (FA) and TG profiles differed between sexes in both fat pads, with longer chain FAs and TGs in males compared to that in females. Remarkably, hepatic phospholipid composition was sex dependent with more abundant lipotoxic FAs in males than in females. This may contribute to the sexual dimorphism in response to obesity towards more metaflammation in males. Our work presents an exhaustive novel description of a sex-specific lipid signature in the pathophysiology of metabolic disorders associated with obesity in ob/ob mice. These data could settle the basis for future pharmacological treatment in obesity.

Keywords

• Lipidomics
• Fatty acids
• Obesity
• Metabolic syndrome
• Sex