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Long‐term caloric restriction ameliorates deleterious effects of aging on white and brown adipose tissue plasticity
Authors:Patricia Corrales  Yurena Vivas  Adriana Izquierdo‐Lahuerta  Daniel Horrillo  Patricia Seoane‐Collazo  Ismael Velasco  Lucia Torres  Yamila Lopez  Carmen Martínez  Miguel Lpez  Manuel Ros  Maria Jesus Obregon  Gema Medina‐Gomez
Institution:Patricia Corrales,Yurena Vivas,Adriana Izquierdo‐Lahuerta,Daniel Horrillo,Patricia Seoane‐Collazo,Ismael Velasco,Lucia Torres,Yamila Lopez,Carmen Martínez,Miguel López,Manuel Ros,Maria Jesus Obregon,Gema Medina‐Gomez
Abstract:Age‐related increased adiposity is an important contributory factor in the development of insulin resistance (IR) and is associated with metabolic defects. Caloric restriction (CR) is known to induce weight loss and to decrease adiposity while preventing metabolic risk factors. Here, we show that moderate 20% CR delays early deleterious effects of aging on white and brown adipose tissue (WAT and BAT, respectively) function and improves peripheral IR. To elucidate the role of CR in delaying early signs of aging, young (3 months), middle‐aged (12 months), and old (20 months) mice fed al libitum and middle‐aged and old mice subjected to early‐onset CR were used. We show that impaired plasticity of subcutaneous WAT (scWAT) contributes to IR, which is already evident in middle‐aged mice. Moreover, alteration of thyroid axis status with age is an important factor contributing to BAT dysfunction in middle‐aged animals. Both defects in WAT and BAT/beige cells are ameliorated by CR. Accordingly, CR attenuated the age‐related decline in scWAT function and decreased the extent of fibro‐inflammation. Furthermore, CR promoted scWAT browning. In brief, our study identifies the contribution of scWAT impairment to age‐associated metabolic dysfunction and identifies browning in response to food restriction, as a potential therapeutic strategy to prevent the adverse metabolic effects in middle‐aged animals.
Keywords:adipose tissue  aging  caloric restriction  fibro‐inflammation  insulin resistance  thyroid hormone
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