Sex Differences in High Fat Diet-Induced Metabolic Alterations Correlate with Changes in the Modulation of GRK2 Levels

被引:19
作者
Arcones, Alba C. [1 ,2 ,3 ,4 ]
Cruces-Sande, Marta [1 ,2 ,3 ,4 ]
Ramos, Paula [3 ,4 ]
Mayor, Federico, Jr. [1 ,2 ,3 ,4 ]
Murga, Cristina [1 ,2 ,3 ,4 ]
机构
[1] Inst Invest Sanitaria La Princesa, Madrid 28006, Spain
[2] ISCIII, CIBER Enfermedades Cardiovasc CIBERCV, Madrid 28029, Spain
[3] CSIC UAM, Dept Biol Mol, Madrid 28049, Spain
[4] CSIC UAM, Ctr Biol Mol Severo Ochoa, Madrid 28049, Spain
关键词
sex-related differences; estrogens; GRK2; insulin resistance; obesity; metabolic diseases; diabetes; PROTEIN-COUPLED RECEPTOR; INSULIN-RESISTANCE; KINASE; ESTROGEN; HEALTH; HOMEOSTASIS; OBESITY; MODELS; IMPACT;
D O I
10.3390/cells8111464
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A differential sex-related sensitivity has been reported in obesity and insulin resistance-related cardio-metabolic diseases, with a lower incidence of these pathologies being observed in young females when compared to age-matched males. However, such relative protection is lost with age. The mechanisms underlying such sex and age-related changes in the susceptibility to diabetes and obesity are not fully understood. Herein, we report that the relative protection that is displayed by young female mice, as compared to male littermates, against some of the metabolic alterations that are induced by feeding a high fat diet (HFD), correlates with a lower upregulation of the protein levels of G protein-coupled receptor kinase (GRK2), which is a key regulator of both insulin and G protein-coupled receptor signaling, in the liver and adipose tissue. Interestingly, when the HFD is initiated in middle-aged (32 weeks) female mice, these animals are no longer protected and display a more overt obese and insulin-resistant phenotype, along with a more evident increase in the GRK2 protein levels in metabolically relevant tissues in such conditions. Our data suggest that GRK2 dosage might be involved in the sex and age-biased sensitivity to insulin resistance-related pathologies.
引用
收藏
页数:15
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