EFFICACY OF HYPERBARIC OXYGEN THERAPY ON REGENERATION OF MANDIBULAR BONY DEFECTS IN RATS WITH INDUCED DIABETES MELLITUS

Rodina H. Eldisoky, Salwa Younes, Samia Omar, Hagar S. Gharib, Tarek A. Tamara
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Abstract

INTRODUCTION: Bone repair abnormalities have been associated with diabetes mellitus (DM), including inhibited osteoblastic differentiation, induced osteoblast apoptosis, and compromised angiogenesis. Thus, restoring critical-sized defects is challenging in clinical practice, especially in people with diabetes. Hyperbaric oxygen therapy (HBOT) can be used together with bone grafts to reconstruct these defects. OBJECTIVES: To evaluate the effect of HBOT on the regeneration of critical-sized defects in rats with induced diabetes mellitus. MATERIALS AND METHODS: Twelve adult male albino rats were divided into two groups of 6 animals each. Animals in both groups were given a single intraperitoneal injection of streptozotocin to induce DM. Critical-sized defects were created in the posterior mandibles and filled with beta-tricalcium phosphate (β -TCP). The study group was subjected to HBOT at (2.4 ATA) for 5 days per week for 90 minutes each. Animals were euthanized one week postoperatively. Bone regeneration was assessed histologically and histomorphometrically. Angiogenesis was evaluated by immunohistochemistry against vascular endothelial progenitor cell marker (CD34), and the microvessel density (MVD) was calculated. RESULTS: Histological and immunohistochemical results revealed superior bone regeneration and angiogenesis in the study group. These results were further confirmed by the histomorphometrical analysis which showed higher MVD and new bone surface area in the study group compared to the control group. CONCLUSIONS: HBOT enhanced bone regeneration, improved the regenerative effect of β -TCP, and increased angiogenesis in the defects.
高压氧疗法对糖尿病大鼠下颌骨缺损再生的疗效
骨修复异常与糖尿病(DM)相关,包括成骨细胞分化抑制、成骨细胞凋亡诱导和血管生成受损。因此,在临床实践中,修复临界尺寸的缺陷是具有挑战性的,特别是在糖尿病患者中。高压氧治疗(HBOT)可配合骨移植重建这些缺损。目的:探讨HBOT对诱导型糖尿病大鼠临界尺寸缺损再生的影响。材料与方法:将12只成年雄性白化大鼠分为两组,每组6只。两组动物均给予单次腹腔注射链脲佐菌素诱导糖尿病。在后下颌形成临界大小的缺损,并用β -磷酸三钙(β -TCP)填充。实验组接受(2.4 ATA) HBOT,每周5天,每次90分钟。术后1周对动物实施安乐死。用组织学和组织形态学方法评估骨再生。采用免疫组化方法检测血管内皮祖细胞标志物(CD34)的新生情况,计算微血管密度(MVD)。结果:组织学和免疫组化结果显示实验组骨再生和血管生成能力较强。组织形态学分析进一步证实了这一结果,实验组的MVD和新骨表面积均高于对照组。结论:HBOT能促进骨再生,提高β -TCP的再生效果,促进骨缺损血管生成。
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