Regulation of bone mass, bone loss and osteoclast activity by cannabinoid receptors

Aymen I Idris, Robert J van 't Hof, Iain R Greig, Susan A Ridge, David Baker, Ruth A Ross, Stuart H Ralston

Research output: Contribution to journalArticlepeer-review

Abstract

Accelerated osteoclastic bone resorption has a central role in the pathogenesis of osteoporosis and other bone diseases. Identifying the molecular pathways that regulate osteoclast activity provides a key to understanding the causes of these diseases and to the development of new treatments. Here we show that mice with inactivation of cannabinoid type 1 (CB1) receptors have increased bone mass and are protected from ovariectomy-induced bone loss. Pharmacological antagonists of CB1 and CB2 receptors prevented ovariectomy-induced bone loss in vivo and caused osteoclast inhibition in vitro by promoting osteoclast apoptosis and inhibiting production of several osteoclast survival factors. These studies show that the CB1 receptor has a role in the regulation of bone mass and ovariectomy-induced bone loss and that CB1- and CB2-selective cannabinoid receptor antagonists are a new class of osteoclast inhibitors that may be of value in the treatment of osteoporosis and other bone diseases.
Original languageEnglish
Pages (from-to)774-9
Number of pages6
JournalNature Medicine
Volume11
Issue number7
DOIs
Publication statusPublished - 2005

Keywords

  • Animals
  • Apoptosis
  • Bone Density
  • Bone Resorption
  • Bone and Bones
  • Bornanes
  • Carrier Proteins
  • Cells, Cultured
  • Female
  • Indoles
  • Ligands
  • Membrane Glycoproteins
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Osteoclasts
  • Ovariectomy
  • Piperidines
  • Pyrazoles
  • RANK Ligand
  • Rabbits
  • Receptor Activator of Nuclear Factor-kappa B
  • Receptor, Cannabinoid, CB1
  • Receptor, Cannabinoid, CB2

Fingerprint

Dive into the research topics of 'Regulation of bone mass, bone loss and osteoclast activity by cannabinoid receptors'. Together they form a unique fingerprint.

Cite this