| Literature DB >> 21701078 |
Koichiro Satoh1, Hans Mark, Peter Zachrisson, Björn Rydevik, Gunnar Byröd, Shin-Ichi Kikuchi, Shin-Ichi Konno, Miho Sekiguchi.
Abstract
Low doses of methotrexate (MTX) are safe and effective for treating adult and juvenile rheumatoid arthritis. However, because this powerful anti-inflammatory drug might negatively influence the healing of wounds and fractures, MTX administration is often stopped during surgical procedures. The present study assesses the effects of low- and high-dose MTX on early inflammatory processes and bone healing in an experimental model of fracture. Thirty male Sprague-Dawley rats were assigned to low- and high-dose MTX and control groups. A femur was cut using a reciprocating saw and a 2-mm fracture gap was made using a fixator. One or four weeks thereafter, macrophages were immunostained and new bone formation was histomorphometrically measured. Significantly less new bone was formed in the high-dose MTX, than in the control group (p< 0.01), whereas bone formation did not significantly differ between the low-dose MTX and control groups. These results suggested that a low dose of MTX does not affect the early process of endochondral bone formation during fracture healing, whereas a high dose might delay the progress of new periosteal bone formation. Although more macrophages were found in the groups treated with MTX, their impact on surrounding inflammatory processes remains unclear.Entities:
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Year: 2011 PMID: 21701078 DOI: 10.5387/fms.57.11
Source DB: PubMed Journal: Fukushima J Med Sci ISSN: 0016-2590