Akademik Veri Yönetim Sistemi
INTERNATIONAL JOURNAL OF RADIATION RESEARCH, cilt.12, sa.3, ss.229-233, 2014 (SCI-Expanded)
Background: Vitamin D, especially its most active metabolite 1,25-dihydroxyvitannin D-3(Vit D) is essential in regulating a wide variety of biologic processes, such as regulating nnesangial cell activation. The objective of this study was to assess the histopathological changes of effectiveness of Vit D as a protective agent against radiation induced lung injury. Materials and Methods: Eighteen Wistar rats were divided into three groups: control group (group 1:4 rats), irradiation alone group (group 2:7 rats) and irradiation+vit D (group 3:7 rats). Rats in group 2 and 3 were exposed to 20 Gy radiations to the right lung in a Co-60 radiotherapy machine under general anesthesia. Additionally, rats in group 3 received Vit D at a single dose of 0.2 nncg injected IM 2 hours before exposure to irradiation. Rats were sacrificed and lungs were dissected fifty days after post-irradiation. Myofibroblasts and vitamin D3 receptors (VDR) in extracted lungs were stained by innnnunohistochennistry using alpha-smooth muscle actin (SMA) and VDR antibodies. Blinded histological evaluation was performed to assess lung injury. Lung injury was assessed by the acute lung injury score and nnyofibroblastic differentiation score. Results: Acute lung injury scores and nnyofibroblastic differentiation scores were significantly lower in the radiation+vit D group compared to irradiation alone group (p=0.001 and p=0.001, respectively). Conclusion: This study indicates that administration of vit D plays a protective role against acute lung injury through blocking nnyofibroblastic differentiation.