The Anticipated Effect of Glycogen Synthase kinase 3 (GSK3) Antagonist on Pulp Tissue Repair in Rabbits

Fatema Elturki, M. Farid, H. Adawy
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Abstract

Purpose: To investigate the effect of Glycogen Synthase Kinase-3 (GSK3) antagonist on pulp tissue repair in rabbits. Materials and Methods: 24 adult healthy male rabbits were used in this study divided into three main groups: Group I (control): 2 rabbits with normal teeth without pulp exposure. Group II (TG): The exposed pulps of right posterior teeth of 22 rabbits were capped with KolSpon in association with 34 nM Tideglusib. Group III (MTA): The exposed pulps of left posterior teeth of 22 rabbits were capped with Mineral Trioxide Aggregate (MTA). The 2 rabbits with normal teeth and 6 rabbits with pulp capped posterior teeth were euthanized after one day. Their DNAs were extracted and tested for expression of Axin2 and β-actin by qPCR. 8 rabbits were euthanized after 4 weeks, and another 8 was euthanized after 6 weeks. The teeth were collected and prepared for immunohistochemical study using antiβ-catenin antibody. Results: The qPCR results showed the higher expression of Axin2 in the Tideglusib group than control group (without treatment) by about 5 folds and about 1.5 fold in the MTA group. The immunohistochemical results revealed the increase intensity in the Tideglusib group than MTA at four weeks with no significance difference (p>0.05).Whilst after 6 weeks the higher expression was in Tideglusib group with significance difference (p<0.05). Conclusion: The Tideglusib drug stimulates the expression of Axin2 transcription factor gene which is known to play a key role in regulation of odontoblast and osteoblast differentiation.
糖原合成酶激酶3 (GSK3)拮抗剂对兔牙髓组织修复的预期作用
目的:探讨糖原合成酶激酶3 (GSK3)拮抗剂对兔牙髓组织修复的影响。材料与方法:选取健康成年雄性家兔24只,分为三组:第一组(对照组):2只牙正常,无牙髓外露。第二组(TG): 22只家兔右后牙外露牙髓,用KolSpon联合34 nM Tideglusib覆盖。第三组(MTA): 22只家兔左后牙外露牙髓用三氧化矿骨料(MTA)覆盖。正常牙2只,后牙盖髓6只,1 d后安乐死。提取其dna, qPCR检测Axin2和β-actin的表达。4周后处死8只,6周后处死8只。收集牙齿,用抗β-连环蛋白抗体进行免疫组化研究。结果:qPCR结果显示,Tideglusib组Axin2的表达比对照组(未处理)高约5倍,MTA组Axin2的表达比对照组(未处理)高约1.5倍。免疫组化结果显示,第4周时,Tideglusib组的强度明显高于MTA组,但差异无统计学意义(p>0.05)。6周后,Tideglusib组表达量较高,差异有统计学意义(p<0.05)。结论:Tideglusib药物可刺激Axin2转录因子基因的表达,该基因在成牙细胞和成骨细胞分化中起关键作用。
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