Role of oestrogen receptor signaling in skeletal response to leptin in female ob/ob mice

Leptin, critical in regulation of energy metabolism, is also important for normal bone growth, maturation and turnover. Compared to wild type (WT) mice, bone mass is lower in leptin-deficient ob/ob mice; osteopenia in growing ob/ob mice is due to decreased bone accrual, and is associated with reduced longitudinal bone growth, impaired cancellous bone maturation and increased marrow adipose tissue (MAT). However, leptin deficiency also results in gonadal dysfunction, disrupting production of gonadal hormones which regulate bone growth and turnover. The present study evaluated the role of increased oestrogen in mediating the effects of leptin on bone in ob/ob mice. Three-month-old female ob/ob mice were randomized into one of 3 groups: (1) ob/ob+vehicle (veh), (2) ob/ob+leptin (leptin), or (3) ob/ob+leptin and the potent oestrogen receptor antagonist ICI 182,780 (leptin+ICI). Age-matched WT mice received vehicle. Leptin (40 µg/mouse, daily) and ICI (10 µg/mouse, 2x/w) were administered by sc injection for 1 month and bone analyzed by x-ray absorptiometry, microcomputed tomography, and static and dynamic histomorphometry. Uterine weight did not differ between ob/ob mice and ob/ob mice receiving leptin+ICI, indicating that ICI successfully blocked the uterine response to leptin-induced increases in oestrogen levels. Compared to leptin-treated ob/ob mice, ob/ob mice receiving leptin+ICI had lower uterine weight, did not differ in weight loss, MAT, or bone formation rate, and had higher longitudinal bone growth rate and cancellous bone volume fraction. We conclude that increased oestrogen signaling following leptin treatment is dispensable for the positive actions of leptin on bone and may attenuate leptin-induced bone growth.

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