Publications [#147434] of Bruce M. Klitzman
- KC Olbrich, R Meade, W Bruno, L Heller, B Klitzman, LS Levin, Halofuginone inhibits collagen deposition in fibrous capsules around implants.,
Annals of plastic surgery, United States, vol. 54 no. 3
pp. 293-6;discussion 296, ISSN 0148-7043
(last updated on 2007/01/02)
Fibrous capsule formation around implants remains a difficult problem that has been studied for decades. The etiology is elusive, but the end result is the deposition of a dense collagenous capsule around implanted materials. The purpose of this study was to determine the effects of a type I collagen synthesis inhibitor, halofuginone, on fibrous capsule formation around implanted materials. Silastic disks were implanted subcutaneously into 4 groups of adult male rats for up to 8 weeks. Group 1 received drug throughout the study, group 2 received drug during the first half only, group 3 received drug during the second half only, and the control group received no drug. Implants were removed and histology of the capsules was examined. A collagen index score was calculated from digital images of trichrome-stained histologic sections, which permitted semiquantitative comparison of collagen content among the 4 groups. The collagen index values clearly indicate that halofuginone effectively inhibited collagen deposition within the capsule around the implanted disks. Halofuginone treatment also resulted in a decrease in the collagen index score in rat skin, indicating that halofuginone may affect preexisting collagenous structures. The ability of halofuginone to inhibit collagen deposition in new and preexisting fibrous capsules suggests that it may be a useful adjunct to minimize the formation of capsules around implantable prostheses.
Animals • Collagen Type I • Colorimetry • Fibrosis • Male • Muscles • Piperidines • Prostheses and Implants* • Protein Synthesis Inhibitors • Quinazolines • Quinazolinones • Rats • Rats, Sprague-Dawley • Silicone Elastomers* • Subcutaneous Tissue • Transforming Growth Factor beta • adverse effects • antagonists & inhibitors* • etiology • metabolism • metabolism* • pathology • pathology* • pharmacology* • prevention & control