Skeletal glucocorticoid signalling determines leptin resistance and obesity in aging mice

• DOI: 10.1016/j.molmet.2020.101098
• Publication Date: 2020-10-10T01:33:37Z
• Authors: Holger Henneicke; Sarah Kim; Michael M. Swarbrick; Jingbao Li; Sylvia J. Gasparini; Joanne Thai; Daphne Foong; Lauryn L. Cavanagh; Colette Fong-Yee; Elisabeth Karsten; Ruby C.Y. Lin; Mark S. Cooper; Hong Zhou; Markus J. Seibel
• Keywords: Leptin; 0301 basic medicine; Aging; Hypothalamus; Mice, Obese; Mice, Transgenic; Bone and Bones; Mice; 03 medical and health sciences; Glucocorticoid; Animals; Insulin; Obesity; Internal medicine; Glucocorticoids; 2. Zero hunger; 0303 health sciences; Osteoblast; Body Weight; Age Factors; Arcuate Nucleus of Hypothalamus; Osteocyte; Brain; RC31-1245; 3. Good health; Mice, Inbred C57BL; Glucose; Adipose Tissue; Body Composition; Original Article; Female; Insulin Resistance

Aging and chronic glucocorticoid excess share a number of critical features, including the development of central obesity, insulin resistance and osteoporosis. Previous studies have shown that skeletal glucocorticoid signalling increases with aging and that osteoblasts mediate the detrimental skeletal and metabolic effects of chronic glucocorticoid excess. Here, we investigated whether endogenous glucocorticoid action in the skeleton contributes to metabolic dysfunction during normal aging.Mice lacking glucocorticoid signalling in osteoblasts and osteocytes (HSD2OB/OCY-tg mice) and their wild-type littermates were studied until 3, 6, 12 and 18 months of age. Body composition, adipose tissue morphology, skeletal gene expression and glucose/insulin tolerance were assessed at each timepoint. Leptin sensitivity was assessed by arcuate nucleus STAT3 phosphorylation and inhibition of feeding following leptin administration. Tissue-specific glucose uptake and adipose tissue oxygen consumption rate were also measured.As they aged, wild-type mice became obese and insulin-resistant. In contrast, HSD2OB/OCY-tg mice remained lean and insulin-sensitive during aging. Obesity in wild-type mice was due to leptin resistance, evidenced by an impaired ability of exogenous leptin to suppress food intake and phosphorylate hypothalamic STAT3, from 6 months of age onwards. In contrast, HSD2OB/OCY-tg mice remained leptin-sensitive throughout the study. Compared to HSD2OB/OCY-tg mice, leptin-resistant wild-type mice displayed attenuated sympathetic outflow, with reduced tyrosine hydroxylase expression in both the hypothalamus and thermogenic adipose tissues. Adipose tissue oxygen consumption rate declined progressively in aging wild-type mice but was maintained in HSD2OB/OCY-tg mice. At 18 months of age, adipose tissue glucose uptake was increased 3.7-fold in HSD2OB/OCY-tg mice, compared to wild-type mice.Skeletal glucocorticoid signalling is critical for the development of leptin resistance, obesity and insulin resistance during aging. These findings underscore the skeleton's importance in the regulation of body weight and implicate osteoblastic/osteocytic glucocorticoid signalling in the aetiology of aging-related obesity and metabolic disease.