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Hormones and Bone Tissue01:17

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Androgens modulate osteocalcin release by human visceral adipose tissue.

Carlo Foresta1, Giacomo Strapazzon, Luca De Toni

  • 1Department of Histology, Microbiology and Medical Biotechnologies, Section of Clinical Pathology and Centre for Male Gamete CryopreservationEndocrine-Metabolic Laboratory (A.S.), Internal Medicine 3, University of PadovaEURAC Institute of Mountain Emergency Medicine (G.S.), Bozen/BolzanoDepartment of Oncological and Surgical Sciences, Clinical Surgery II (A.B), University Hospital of PadovaDepartment of Laboratory Medicine (M.P.), University Hospital of Padova, Padova, Italy.

Clinical Endocrinology
|April 28, 2011
PubMed
Summary

Androgens stimulate osteocalcin (OCN) release from human adipose tissue (AT). This suggests androgens may protect energy metabolism, particularly in obesity where hormone levels are altered.

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Area of Science:

  • Endocrinology
  • Metabolic Research
  • Adipose Tissue Biology

Background:

  • Androgens are known to inhibit fat cell differentiation and promote lipolysis.
  • Undercarboxylated osteocalcin (ucOCN) influences insulin and adiponectin secretion and is produced by adipose tissue.
  • The interplay between androgens, osteocalcin, and adipose tissue in metabolic regulation requires further elucidation.

Purpose of the Study:

  • To investigate the role of androgens in modulating osteocalcin (OCN) release from human adipose tissue (AT).
  • To examine the relationship between androgen levels, body mass index (BMI), and OCN forms in male patients.

Main Methods:

  • Human omental adipose tissue (OAT) was stimulated with dihydrotestosterone (DHT) in vitro, with and without flutamide.
  • The release of carboxylated (cOCN) and undercarboxylated (ucOCN) forms of osteocalcin by OAT was measured using ELISA.
  • Serum levels of total and free testosterone, ucOCN, and cOCN were measured in 91 male patients.

Main Results:

  • DHT stimulation significantly increased the release of both cOCN and ucOCN from OAT.
  • Flutamide co-incubation abolished the DHT-induced increase in OCN production.
  • Overweight and obese patients exhibited lower total and free testosterone, associated with reduced ucOCN and a lower ucOCN/OCN ratio.

Conclusions:

  • Androgens directly modulate osteocalcin release from human adipose tissue in vitro.
  • Androgens may offer a protective effect on energy metabolism through OCN modulation, a novel mechanism beyond their known anti-adipogenic effects.
  • Given altered sex hormone levels in obesity and adipose tissue's role in hormone clearance and OCN production, this interaction is particularly significant for metabolic health.