Edinburgh Research Explorer

Expansion of bone marrow adipose tissue during caloric restriction is associated with increased circulating glucocorticoids and not with hypoleptinemia.

Research output: Contribution to journalArticle

  • William P. Cawthorn
  • Erica L. Scheller
  • Sebastian D. Parlee
  • Hoai An Pham
  • Brian S. Learman
  • Catherine Redshaw
  • Richard Sulston
  • Aaron Burr
  • Arun Das
  • Becky R. Simon
  • Hiroyuki Mori
  • Adam J. Bree
  • Benjamin Schell
  • Venkatesh Krishnan
  • Ormond A. MacDougald

Related Edinburgh Organisations

Open Access permissions

Open

Documents

Original languageEnglish
Article number26696121
Pages (from-to)508-521
JournalEndocrinology
Volume157
Issue number2
Early online date22 Dec 2015
DOIs
Publication statusPublished - 1 Feb 2016

Abstract

Bone marrow adipose tissue (MAT) accounts for up to 70% of bone marrow volume in healthy adults and increases further in clinical conditions of altered skeletal or metabolic function. Perhaps most strikingly, and in stark contrast to white adipose tissue (WAT), MAT has been found to increase during caloric restriction (CR) in humans and many other species. Hypoleptinemia may drive MAT expansion during CR but this has not been demonstrated conclusively. Indeed, MAT formation and function are poorly understood; hence, the physiological and pathological roles of MAT remain elusive. We recently revealed that MAT contributes to hyperadiponectinemia and systemic adaptations to CR. To further these observations, we have now performed CR studies in rabbits to determine if CR affects adiponectin production by MAT. Moderate or extensive CR decreased bone mass, WAT mass, and circulating leptin, but, surprisingly, did not cause hyperadiponectinemia or MAT expansion. Although this unexpected finding limited our subsequent MAT characterization, it demonstrates that during CR, bone loss can occur independently of MAT expansion; increased MAT may be required for hyperadiponectinemia; and hypoleptinemia is not sufficient for MAT expansion. We further investigated this relationship in mice. In females, CR increased MAT without decreasing circulating leptin, suggesting that hypoleptinemia is also not necessary for MAT expansion. Finally, circulating glucocorticoids increased during CR in mice but not rabbits, suggesting that glucocorticoids might drive MAT expansion during CR. These observations provide insights into the causes and consequences of CR-associated MAT expansion, knowledge with potential relevance to health and disease.

    Research areas

  • Bone marrow adipose tissue, caloric restriction, glucocorticoids, adiponectin, leptin

Download statistics

No data available

ID: 23043737