中国骨质疏松杂志
中國骨質疏鬆雜誌
중국골질소송잡지
Chinese Journal of Osteoporosis
2015年
10期
1201-1207,1229
,共8页
马育林%张建东%吴凤%袁妙兰%盛志峰%陈宏
馬育林%張建東%吳鳳%袁妙蘭%盛誌峰%陳宏
마육림%장건동%오봉%원묘란%성지봉%진굉
地塞米松%生长期小鼠%骨微结构%骨代谢%骨密度
地塞米鬆%生長期小鼠%骨微結構%骨代謝%骨密度
지새미송%생장기소서%골미결구%골대사%골밀도
Dexamethesone%Growing mouse%Bone microstructure%Bone metabolism%Bone mineral density
目的:观察小剂量地塞米松对生长期小鼠骨微结构及骨代谢的影响。方法24只4周龄雌性小鼠随机分两组( n=12):地塞米松组(DEX,1 mg/kg,肌肉注射,2次/周),对照组。4 w后处死小鼠,检测血清Ⅰ型前胶原N端肽(PINP)和骨Ⅰ型胶原交联C端肽(β?CTX)蛋白的表达水平;检测胫骨干骺端骨保护素( OPG)、核因子?κ B受体活化因子配体( RANKL)表达;抗酒石酸酸性磷酸酶( TRAP)染色方法检测破骨细胞;一侧胫骨行显微CT扫描分析。结果 DEX组小鼠胫表观骨密度和骨体积分数明显高于对照组(P<0?05),骨小梁数量高于对照组,结构模型指数低于对照组,但无统计学意义。 DEX组小鼠血清PINP及β?CTX浓度显著下降(P<0?05)。 DEX组小鼠胫骨干骺端OPG表达明显增多,而RANKL表达无明显变化,相对于对照组,OPG/RANKL比值升高。 TRAP染色示DEX组小鼠胫骨干骺端破骨细胞数量较对照组减少。结论小剂量地塞米松间断给药可能通过上调OPG/RANKL比率维持生长期小鼠骨量。
目的:觀察小劑量地塞米鬆對生長期小鼠骨微結構及骨代謝的影響。方法24隻4週齡雌性小鼠隨機分兩組( n=12):地塞米鬆組(DEX,1 mg/kg,肌肉註射,2次/週),對照組。4 w後處死小鼠,檢測血清Ⅰ型前膠原N耑肽(PINP)和骨Ⅰ型膠原交聯C耑肽(β?CTX)蛋白的錶達水平;檢測脛骨榦骺耑骨保護素( OPG)、覈因子?κ B受體活化因子配體( RANKL)錶達;抗酒石痠痠性燐痠酶( TRAP)染色方法檢測破骨細胞;一側脛骨行顯微CT掃描分析。結果 DEX組小鼠脛錶觀骨密度和骨體積分數明顯高于對照組(P<0?05),骨小樑數量高于對照組,結構模型指數低于對照組,但無統計學意義。 DEX組小鼠血清PINP及β?CTX濃度顯著下降(P<0?05)。 DEX組小鼠脛骨榦骺耑OPG錶達明顯增多,而RANKL錶達無明顯變化,相對于對照組,OPG/RANKL比值升高。 TRAP染色示DEX組小鼠脛骨榦骺耑破骨細胞數量較對照組減少。結論小劑量地塞米鬆間斷給藥可能通過上調OPG/RANKL比率維持生長期小鼠骨量。
목적:관찰소제량지새미송대생장기소서골미결구급골대사적영향。방법24지4주령자성소서수궤분량조( n=12):지새미송조(DEX,1 mg/kg,기육주사,2차/주),대조조。4 w후처사소서,검측혈청Ⅰ형전효원N단태(PINP)화골Ⅰ형효원교련C단태(β?CTX)단백적표체수평;검측경골간후단골보호소( OPG)、핵인자?κ B수체활화인자배체( RANKL)표체;항주석산산성린산매( TRAP)염색방법검측파골세포;일측경골행현미CT소묘분석。결과 DEX조소서경표관골밀도화골체적분수명현고우대조조(P<0?05),골소량수량고우대조조,결구모형지수저우대조조,단무통계학의의。 DEX조소서혈청PINP급β?CTX농도현저하강(P<0?05)。 DEX조소서경골간후단OPG표체명현증다,이RANKL표체무명현변화,상대우대조조,OPG/RANKL비치승고。 TRAP염색시DEX조소서경골간후단파골세포수량교대조조감소。결론소제량지새미송간단급약가능통과상조OPG/RANKL비솔유지생장기소서골량。
Objective To observe the effects of low?dose dexamethesone on bone microachitecture and metabolism in growing period mice. Methods Twenty?four 4?week?old female mice were randomLy assigned to two groups ( n=12 ): Dexamethesone group (DEX, 1mg/kg, intramuscularly injected, twice/w); and the control group. 4 weeks after treatment, all the mice were sacrificed Serum aminoterminal propeptide of type I procollagen ( PINP) and carboxy?terminal telopeptide of type I collagen ( CTX) were measured by enzyme linked immunoabsorbent assay ( ELISA ) . OPG and RANKL of metaphyseal were detected by immunohistochemistry analysis. One tibia of each mouse was selected for microCT analysis. Results Trabecular aBMD and bone volume fraction of the femur significantly increased in DEX group than that of the control group(P<0?05). Trabecular number and structure model index increased in the DEX group, while there was no significant difference between two groups. In contrast to th control mice, serum PINP and CTX significantly decreased in DEX mice ( P < 0?05 ) OPG expression in tibia metaphyseal significantly increased in DEX mice, but there was no significant change in RANKL expression. And OPG/RANKL ratio significantly increased in DEX mice. In contrast to the control mice, the number of osteoclasts of tibia metaphyseal in DEX mice decreased. Conclusion Intermittent administration of low?dose dexamethasone may maintain bone mass in growing mice by upregulating OPG/RANKL ratio.