z-logo
Premium
Systemic treatment with the sphingosine‐1‐phosphate analog FTY720 does not improve fracture healing in mice
Author(s) -
Heilmann Aline,
Schinke Thorsten,
Bindl Ronny,
Wehner Tim,
Rapp Anna,
HaffnerLuntzer Melanie,
Liedert Astrid,
Amling Michael,
Ignatius Anita
Publication year - 2013
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.22426
Subject(s) - bone healing , osteoclast , medicine , sphingosine 1 phosphate , osteoblast , bone remodeling , femur fracture , tartrate resistant acid phosphatase , osteotomy , endocrinology , pharmacology , sphingosine , femur , surgery , receptor , chemistry , biochemistry , in vitro
Abstract Sphingosine‐1‐phosphate (S1P) has recently been recognized as a crucial coupling molecule of osteoclast and osteoblast activity provoking osteoanabolic effects. Targeting S1P receptors could, therefore, be a potential strategy to support bone formation in osteopenic diseases or in fracture repair. Here we investigated whether systemic treatment with the S1P analog FTY720 (Fingolimod) could improve fracture healing. Twelve‐week‐old, female C57BL/6 mice received an osteotomy of the femur, which was stabilized using an external fixator. The mice received a daily subcutaneous injection of either FTY720 (6 mg/kg) or vehicle from the third postoperative day. Fracture healing was evaluated after 10 and 21 days using biomechanical testing, µ‐computed tomography, and histomorphometry. Because FTY720 is supposed to influence osteoclast recruitment, osteoclasts were identified in the fracture callus by staining for tartrate resistant acid phosphatase (TRAP). There were no significant differences in callus mechanical properties, tissue composition and osteoclast number between the groups, suggesting that systemically applied FTY720 did not influence bone regeneration in this model of regular fracture healing. Even if further studies should test the potency of FTY720 under unfavorable healing conditions, we conclude that the effect of systemically applied FTY720 on fracture healing might be inferior compared to other anabolic treatments. © 2013 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 31:1845–1850, 2013

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here