Additive bone-protective effects of anabolic treatment when used in conjunction with RANKL and tumor necrosis factor inhibition in two rat arthritis models

Arthritis Rheum. 2005 May;52(5):1604-11. doi: 10.1002/art.21021.

Abstract

Objective: To investigate whether the bone-preserving effects of a RANKL antagonist or a tumor necrosis factor (TNF) antagonist could be further improved by the addition of a bone anabolic agent in inflammatory arthritis.

Methods: Lewis rats with either adjuvant-induced arthritis (AIA) or collagen-induced arthritis (CIA) were treated for 10 days with PEGylated soluble tumor necrosis factor receptor type I (PEG sTNFRI), interleukin-1 receptor antagonist (IL-1Ra), osteoprotegerin (OPG), parathyroid hormone (PTH), or combinations of these agents starting on day 4 after disease onset. Treatment effects were assessed clinically, radiologically, and histologically, and by morphometry for the extent of paw swelling, bone erosive changes, and synovial inflammation.

Results: Paw swelling and synovial inflammation were significantly inhibited by PEG sTNFRI in AIA and CIA, and by IL-1Ra in CIA. OPG and PTH had no significant effect on these parameters. Analysis of bone erosion revealed a significant bone-sparing effect of monotherapy with PEG sTNFRI or OPG in both models, whereas IL-1Ra was only effective in CIA. PTH treatment alone did not show a bone-protective effect in either model. With the combination of PEG sTNFRI and PTH, erosion scores (-74% in AIA and -61% in CIA versus controls) were significantly lower than those elicited by PEG sTNFRI alone (-41% and -29%, respectively, versus controls). Similar results were also obtained with the combination of OPG and PTH (-88% in AIA and -73% in CIA, compared with -70% and -55%, respectively, with OPG monotherapy). Coadministration of IL-1Ra and PTH had no synergistic bone-sparing effect. Morphometric analysis revealed that the addition of PTH to PEG sTNFRI or OPG resulted in higher bone volume and higher osteoblast numbers in both AIA and CIA.

Conclusion: The bone-protective effects resulting from RANKL or TNF antagonism can be further improved by the addition of a bone anabolic agent.

MeSH terms

  • Animals
  • Arthritis / drug therapy*
  • Bone Development / drug effects
  • Bone Diseases / prevention & control*
  • Bone Resorption / prevention & control
  • Carrier Proteins / antagonists & inhibitors*
  • Cell Count
  • Disease Models, Animal
  • Drug Synergism
  • Female
  • Glycoproteins / pharmacology*
  • Male
  • Membrane Glycoproteins / antagonists & inhibitors*
  • Osteoblasts
  • Osteoprotegerin
  • Parathyroid Hormone / pharmacology
  • Parathyroid Hormone / therapeutic use*
  • Polyethylene Glycols / pharmacology
  • Polyethylene Glycols / therapeutic use*
  • RANK Ligand
  • Rats
  • Rats, Inbred Lew
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Tumor Necrosis Factor
  • Receptors, Tumor Necrosis Factor, Type I / therapeutic use*
  • Tumor Necrosis Factor-alpha* / antagonists & inhibitors*

Substances

  • Carrier Proteins
  • Glycoproteins
  • Membrane Glycoproteins
  • Osteoprotegerin
  • PEGylated tumor necrosis factor alpha receptor 1
  • Parathyroid Hormone
  • RANK Ligand
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Tumor Necrosis Factor
  • Receptors, Tumor Necrosis Factor, Type I
  • Tnfrsf11b protein, rat
  • Tumor Necrosis Factor-alpha
  • Polyethylene Glycols