Your browser doesn't support javascript.
loading
Interleukin 1 Receptor 1 Knockout and Maternal High Fat Diet Exposure Induces Sex-Specific Effects on Adipose Tissue Adipogenic and Inflammatory Gene Expression in Adult Mouse Offspring.
Bridge-Comer, Pania E; Plows, Jasmine F; Ramzan, Farha; Patel, Rachna; Ganapathy, Thashma P; Stanley, Joanna L; Vickers, Mark H; Reynolds, Clare M.
Afiliación
  • Bridge-Comer PE; Developmental Programming Research Group, The Liggins Institute, The University of Auckland, Auckland, New Zealand.
  • Plows JF; Developmental Programming Research Group, The Liggins Institute, The University of Auckland, Auckland, New Zealand.
  • Ramzan F; Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA, United States.
  • Patel R; Developmental Programming Research Group, The Liggins Institute, The University of Auckland, Auckland, New Zealand.
  • Ganapathy TP; Developmental Programming Research Group, The Liggins Institute, The University of Auckland, Auckland, New Zealand.
  • Stanley JL; Developmental Programming Research Group, The Liggins Institute, The University of Auckland, Auckland, New Zealand.
  • Vickers MH; Developmental Programming Research Group, The Liggins Institute, The University of Auckland, Auckland, New Zealand.
  • Reynolds CM; Developmental Programming Research Group, The Liggins Institute, The University of Auckland, Auckland, New Zealand.
Front Physiol ; 11: 601, 2020.
Article en En | MEDLINE | ID: mdl-32655404
ABSTRACT

Background:

The global incidence of obesity continues to rise, increasing the prevalence of metabolic diseases such as insulin resistance, dyslipidemia, and type 2 diabetes mellitus. Low-grade chronic inflammation, associated with the obese state, also contributes to the development of these metabolic comorbidities. Interleukin-1-receptor-1 (IL-1R1), a pro-inflammatory mediator, bridges the metabolic and inflammatory systems. In young male mice, deficiency of IL-1R1 (IL-1R1-/-) paired with a high-fat diet (HFD) offered beneficial metabolic effects, however in female mice, the same pairing led to metabolic dysfunction. Therefore, we examined the contribution of maternal HFD in combination with IL1R1-/- to metabolic health in adult offspring.

Methods:

Female C57BL/6 and IL-1R1-/- mice were randomly assigned to a control diet (10% kcal from fat) or HFD (45% kcal from fat) 10 days prior to mating and throughout gestation and lactation. Male and female offspring were housed in same-sex pairs post-weaning and maintained on control diets until 16 weeks old. At 15 weeks, an oral glucose tolerance test (OGTT) was performed to assess glucose tolerance. Histological analysis was carried out to assess adipocyte size and gene expression of adipogenic and inflammatory markers were examined.

Results:

IL-1R1-/- contributed to increased body weight in male and female adult offspring, irrespective of maternal diet. IL-1R1-/- and maternal HFD increased adipocyte size in the gonadal fat depot of female, but not male offspring. In female offspring, there was reduced expression of genes involved in adipogenesis and lipid metabolism in response to IL1R1-/- and maternal HFD. While there was an increase in inflammatory gene expression in response to maternal HFD, this appeared to be reversed in IL1R1-/- female offspring. In male offspring, there was no significant impact on adipogenic or lipid metabolism pathways. There was an increase in inflammatory gene expression in IL1R1-/- male offspring from HFD-fed mothers.

Conclusion:

This study suggests that IL-1R1 plays a complex and important role in the metabolic health of offspring, impacting adipogenesis, lipogenesis, and inflammation in a sex-specific manner.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Front Physiol Año: 2020 Tipo del documento: Article País de afiliación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Front Physiol Año: 2020 Tipo del documento: Article País de afiliación: Nueva Zelanda