Radiation-induced craniofacial bone growth inhibition: acute and long-term effects on bone histopathology with and without cytoprotection
| Autor: | David A. OʼDonovan, Christopher R. Forrest, Iona Leong, Kenneth H. Pritzker, Ivan Yeung, Marianne Rogers, Maria Mendes, Peter C. Neligan, Cho Y. Pang, Giorgio La Scala |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2012 |
| Předmět: |
Male
Pathology medicine.medical_specialty Osteoblasts/drug effects/pathology/radiation effects Cell Proliferation/drug effects/radiation effects Zygoma/drug effects/growth & development/pathology/radiation effects Radiation-Protective Agents Radiation Dosage Bone remodeling chemistry.chemical_compound Amifostine Periosteum Orbit/drug effects/growth & development/pathology/radiation effects Medicine Animals Periosteum/metabolism/pathology Cell Proliferation Zygoma Osteoblasts ddc:618 business.industry Cell growth Dose-Response Relationship Radiation Cytoprotection Radiation-Protective Agents/pharmacology Amifostine/pharmacology Dose–response relationship Ki-67 Antigen medicine.anatomical_structure chemistry Surgery Histopathology Bone Remodeling Rabbits Growth inhibition business Orbit Ki-67 Antigen/analysis medicine.drug |
| Zdroj: | Plastic and Reconstructive Surgery, Vol. 129, No 4 (2012) pp. 636e-45e |
| ISSN: | 1529-4242 |
| Popis: | The authors previously established an animal model of radiation-induced craniofacial bone growth inhibition and demonstrated the effectiveness of cytoprotection in preserving growth using amifostine, but the mechanism is unclear. The objective of this study was to investigate the acute and long-term histopathologic effects of single-dose orthovoltage irradiation on craniofacial bone with and without cytoprotection.Sixty infant New Zealand White rabbits (7-week-old) were randomized into three groups (n = 20 per group): group 1, 0-Gy, sham irradiation; group 2, 35-Gy single-dose orthovoltage irradiation; and group 3, cytoprotection with amifostine before irradiation. Orbitozygomatic complex bone was harvested from animals 12 hours after irradiation and at skeletal maturity (21 weeks of age). Histologic parameters measured included native bone cell (osteoblast, osteoclast, and osteocyte) populations, periosteal proliferation indices (MIB-1 stains), bone turnover rates [triple fluorochromes: tetracycline administered at 7 weeks of age (before irradiation), alizarin complexone at 12 weeks, and calcein at 16 weeks of age], and endosteal space fibrosis levels.Orthovoltage irradiation significantly (p0.05) reduced osteoblast and osteoclast counts 12 hours after irradiation (age, 7 weeks) with or without pretreatment with amifostine but had no effect on osteocyte populations. Long-term analysis at age 21 weeks demonstrated significantly (p0.05) increased osteoblast counts, reduced endosteal space fibrosis, reduced periosteal proliferation indices, and improved bone turnover (fluorochrome stains) in amifostine-treated animals.This study suggests that amifostine cytoprotection is mediated through a combination of reduced cellular injury with enhanced promotion of cellular bone rebuilding potential. |
| Databáze: | OpenAIRE |
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