High-fat/high-sucrose diet worsens metabolic outcomes and widespread hypersensitivity following early-life stress exposure in female mice

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Abstract
Exposure to stress early in life has been associated with adult-onset comorbidities such as chronic pain, metabolic dysregulation, obesity, and inactivity. We have established an early-life stress model using neonatal maternal separation (NMS) in mice, which displays evidence of increased body weight and adiposity, widespread mechanical allodynia, and hypothalamic-pituitary-adrenal axis dysregulation in male mice. Early-life stress and consumption of a Western-style diet contribute to the development of obesity; however, relatively few preclinical studies have been performed in female rodents, which are known to be protected against diet-induced obesity and metabolic dysfunction. In this study, we gave naïve and NMS female mice access to a high-fat/high-sucrose (HFS) diet beginning at 4 wk of age. Robust increases in body weight and fat were observed in HFS-fed NMS mice during the first 10 wk on the diet, driven partly by increased food intake. Female NMS mice on an HFS diet showed widespread mechanical hypersensitivity compared with either naïve mice on an HFS diet or NMS mice on a control diet. HFS diet-fed NMS mice also had impaired glucose tolerance and fasting hyperinsulinemia. Strikingly, female NMS mice on an HFS diet showed evidence of hepatic steatosis with increased triglyceride levels and altered glucocorticoid receptor levels and phosphorylation state. They also exhibited increased energy expenditure as observed via indirect calorimetry and expression of proinflammatory markers in perigonadal adipose. Altogether, our data suggest that early-life stress exposure increased the susceptibility of female mice to develop diet-induced metabolic dysfunction and pain-like behaviors.
Funding Information
  • HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (U54HD090216)
  • HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD057850)
  • HHS | NIH | NIH Office of the Director (S10OD028598)
  • HHS | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR071263)
  • HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (R01DK103872)
  • HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (K01DK112967)
  • HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (R01DK099611)
  • HHS | NIH | National Institute of General Medical Sciences (P20GM103418)
  • U.S. Department of Veterans Affairs (1IO1BX002567)

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