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The effects of type I collagen on bone defects and gene expression changes for osteogenesis: In a rat model
Authors:Özgür Yiğiter MD  Ali Cagdas Yorukoglu MD  Nilay Şentürk MD  Yavuz Dodurga MD  Ahmet Fahir Demirkan MD
Affiliation:1. Department of Orthopedics and Traumatology, Denizli State Hospital, Denizli, Turkey;2. Department of Orthopedics and Traumatology, Faculty of Medicine, Pamukkale University, Pamukkale, Denizli, Turkey;3. Department of Pathology, Faculty of Medicine, Pamukkale University, Pamukkale, Denizli, Turkey;4. Department of Medical Biology, Pamukkale University, Denizli, Turkey
Abstract:The aim of this study is to investigate the effects of type I collagen on bone defects and on genes specifically for osteogenesis in a rat model. Two millimeter drill hole bone defect was created in the femur of rats. In the experimental group, type I collagen was applied in bone defects whereas in control group defects were left empty. Inflammation, development of connective tissue, osteogenesis, and foreign body reaction parameters evaluated with histologically and genes evaluated by blood samples. In the experimental group, the histopathologically significant change was found in favor of bone healing only at the first week. A significant increase was found in genetic expressions of BMP-1, 2, 3, 4, 5, 6, 7, TGF-βRII, Smad-1, IL-6, BMPR-IA, BMPR-IB, Eng, BMPR-II, c-fos, Cdkn1a, Chrd, Gdf-5, Id-1, PDGF-β, IGF-1, Serpine-1, and TGF-βRI at the first hour. At the first, third, and sixth week, no significant increase was found in any of the gene expressions. Type I collagen is found to be effective in favor of bone healing through increased inflammatory cytokines and expression of BMP genes in the early stages of fracture healing.
Keywords:bone defects  bone morphogenic protein  gene expression  osteogenesis  type I collagen
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