Hypertrophy of vascularized bone isograft in rats treated with cyclosporine A

Calcif Tissue Int. 2003 Oct;73(4):393-9. doi: 10.1007/s00223-002-2147-6. Epub 2003 Jul 30.

Abstract

The aim of this study was to investigate the effects of cyclosporine A (CsA) on vascularized tibio-fibula isograft between 12-week-old male Lewis rats. After transplantation, 45 rats were randomly allocated to one of the following 7 treatment groups: (1) 4-week vehicle (n = 5), (2) 4-week CsA (n = 5), (3) 8-week vehicle (n = 10), (4) 8-week CsA (n = 10), (5) 4-week CsA followed by 4-week vehicle (n = 5), (6) 16-week vehicle (n = 5), or (7) 4-week CsA followed by 12-week vehicle (n = 5). In soft X-ray and micro-computed tomography examination, hypertrophic change of the grafted bones was apparent in the 4- and 8-week CsA groups. Mineral apposition rate and bone formation rate of the grafted bones in the 4-week CsA group were markedly higher than those in the 4-week vehicle group. In the 4- and 8-week CsA groups, however, bone mineral density (BMD) of the grafted bones was lower and strength of the reconstructed bones was weaker than the 4- and 8-week vehicle groups. Urinary deoxypyridinoline (DPD) level was higher in the 4- and 8-week CsA groups than in the 4- and 8-week vehicle groups. The group of 4-week CsA followed by 4-week vehicle had a level of urinary DPD equal to the 8-week vehicle group, but their BMD of the grafted bones was lower and strength of the reconstructed bones was weaker than the 8-week vehicle group. By contrast, the group of 4-week CsA followed by 12-week vehicle had BMD of the grafted bones and strength of the reconstructed bones similar to the 16-week vehicle group. These findings demonstrate that short-term CsA treatment induces hypertrophic change of vascularized bone graft with high-turnover bone loss, and strength of the reconstructed bone is gradually restored after the cessation of CsA treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / urine
  • Animals
  • Biomarkers / analysis
  • Body Weight / drug effects
  • Bone Density / drug effects
  • Bone Transplantation*
  • Cyclosporine / pharmacology*
  • Disease Models, Animal
  • Fibula / blood supply
  • Fibula / pathology
  • Fibula / transplantation
  • Graft Survival / drug effects*
  • Graft Survival / physiology
  • Hypertrophy / diagnostic imaging
  • Hypertrophy / pathology
  • Immunocompromised Host
  • Immunosuppressive Agents / pharmacology*
  • Male
  • Osteogenesis / drug effects
  • Rats
  • Rats, Inbred Lew
  • Tibia / blood supply
  • Tibia / pathology
  • Tibia / transplantation
  • Tomography, X-Ray Computed
  • Transplantation, Isogeneic / pathology

Substances

  • Amino Acids
  • Biomarkers
  • Immunosuppressive Agents
  • Cyclosporine
  • deoxypyridinoline