重庆医学
重慶醫學
중경의학
CHONGQING MEDICAL JOURNAL
2015年
14期
1879-1881
,共3页
钟雯怡%武岐山%高丽%刘琪%陈芳%柴松宏
鐘雯怡%武岐山%高麗%劉琪%陳芳%柴鬆宏
종문이%무기산%고려%류기%진방%시송굉
骨保护素%牙周炎%核因子κB受体活化因子%大鼠 ,Wistar
骨保護素%牙週炎%覈因子κB受體活化因子%大鼠 ,Wistar
골보호소%아주염%핵인자κB수체활화인자%대서 ,Wistar
osteoprotegerin%periodontitis%receptor activator of nuclear factor-kappa B%rats,Wistar
目的:探讨重组人骨保护素(rhOPG)对牙周炎大鼠牙槽骨RANKL、OPG蛋白表达的影响,为rhOPG应用于牙周炎的治疗提供实验依据。方法选择22只Wistar大鼠,采用随机数字表法选择2只健康大鼠作为健康组;其余20只作为实验组,建立牙周炎大鼠模型,再将其分为实验对照组(n=10)和rhOPG组(n=10),rhOPG组大鼠于上颌第2磨牙牙周袋间隙局部注入10 mg/kg rhOPG治疗。实验对照组大鼠于相同部位注射等体积灭菌注射用水。采用链霉素抗生物素蛋白‐过氧化物酶(SP)检测牙槽骨RANKL、OPG蛋白的表达。结果与健康组比较,实验组大鼠牙槽骨OPG表达水平较低,差异有统计学意义(P<0.05),而RANKL表达水平两组差异无统计学意义(P>0.05)。与实验对照组比较,rhOPG组大鼠牙槽骨组织OPG蛋白的表达水平明显上调,而RANKL蛋白的表达明显下调(P<0.05)。治疗后rhOPG组大鼠牙槽骨中OPG表达水平明显高于治疗前,而RANKL表达水平明显低于治疗前,差异有统计学意义(P<0.05)。结论 rhOPG能调节牙周炎大鼠牙槽骨RANKL、OPG的表达。
目的:探討重組人骨保護素(rhOPG)對牙週炎大鼠牙槽骨RANKL、OPG蛋白錶達的影響,為rhOPG應用于牙週炎的治療提供實驗依據。方法選擇22隻Wistar大鼠,採用隨機數字錶法選擇2隻健康大鼠作為健康組;其餘20隻作為實驗組,建立牙週炎大鼠模型,再將其分為實驗對照組(n=10)和rhOPG組(n=10),rhOPG組大鼠于上頜第2磨牙牙週袋間隙跼部註入10 mg/kg rhOPG治療。實驗對照組大鼠于相同部位註射等體積滅菌註射用水。採用鏈黴素抗生物素蛋白‐過氧化物酶(SP)檢測牙槽骨RANKL、OPG蛋白的錶達。結果與健康組比較,實驗組大鼠牙槽骨OPG錶達水平較低,差異有統計學意義(P<0.05),而RANKL錶達水平兩組差異無統計學意義(P>0.05)。與實驗對照組比較,rhOPG組大鼠牙槽骨組織OPG蛋白的錶達水平明顯上調,而RANKL蛋白的錶達明顯下調(P<0.05)。治療後rhOPG組大鼠牙槽骨中OPG錶達水平明顯高于治療前,而RANKL錶達水平明顯低于治療前,差異有統計學意義(P<0.05)。結論 rhOPG能調節牙週炎大鼠牙槽骨RANKL、OPG的錶達。
목적:탐토중조인골보호소(rhOPG)대아주염대서아조골RANKL、OPG단백표체적영향,위rhOPG응용우아주염적치료제공실험의거。방법선택22지Wistar대서,채용수궤수자표법선택2지건강대서작위건강조;기여20지작위실험조,건립아주염대서모형,재장기분위실험대조조(n=10)화rhOPG조(n=10),rhOPG조대서우상합제2마아아주대간극국부주입10 mg/kg rhOPG치료。실험대조조대서우상동부위주사등체적멸균주사용수。채용련매소항생물소단백‐과양화물매(SP)검측아조골RANKL、OPG단백적표체。결과여건강조비교,실험조대서아조골OPG표체수평교저,차이유통계학의의(P<0.05),이RANKL표체수평량조차이무통계학의의(P>0.05)。여실험대조조비교,rhOPG조대서아조골조직OPG단백적표체수평명현상조,이RANKL단백적표체명현하조(P<0.05)。치료후rhOPG조대서아조골중OPG표체수평명현고우치료전,이RANKL표체수평명현저우치료전,차이유통계학의의(P<0.05)。결론 rhOPG능조절아주염대서아조골RANKL、OPG적표체。
Objective To investigate the effects of recombinant human osteoprotegerin(rhOPG) on RANKL ,OPG protein expression in alveolar bone tissue of rats with periodontitis to provide the experimental evidence for the application of rhOPG in pe‐riodontitis treatment .Methods Totally 22 Wistar rats were enrolled .The random number table was adopted to select two healthy rats as the healthy group .The rest 20 rats were selected as the experimental group for establishing the rat models of periodontitis , and then subdivided into the experimental control group (n=10) and rhOPG group (n=10) .Rats in the rhOPG group were locally injected by rhOPG 10 mg/kg at periodontal pocket gap of maxillary second molar ,while those in the experimental control group were injected by sterile water for injection at the same site and some volume .The streptavidin‐perosidase(SP) method was em‐ployed to detect the expression of RANKL ,OPG protein in alveolar bone tissue .Results Compared with the healthy group ,the ex‐pression levels of OPG in alveolar bone tissue of rats in the experimental group were lower with statistically significant difference (P<0 .05) ,while the difference of RANKL expression levels between the two groups showed no statistical significance(P>0 .05) . Compared with the experimental control group ,the expression level of OPG protein in alveolar bone tissue of rats in the rhOPG group was significantly up‐regulated ,while that of RANKL protein was significantly down‐regulated(P<0 .05) .The OPG expres‐sion level after treatment in the rhOPG group was markedly enhanced ,while the RANKL expression level was reduced compared with before treatment ,the difference was statistically significant (P<0 .05) .Conclusion rhOPG may regulates the expression of RANKL and OPG in alveolar bone tissue of rats with periodontitis .