天津医药
天津醫藥
천진의약
TIANJIN MEDICAL JOURNAL
2014年
6期
558-560
,共3页
刘保龙%孙志明%武俏丽%王宏%闫华
劉保龍%孫誌明%武俏麗%王宏%閆華
류보룡%손지명%무초려%왕굉%염화
瘦素%脑脊液%胫骨骨折%骨折愈合%骨密度%原位杂交,荧光%兔%骨形成蛋白2
瘦素%腦脊液%脛骨骨摺%骨摺愈閤%骨密度%原位雜交,熒光%兔%骨形成蛋白2
수소%뇌척액%경골골절%골절유합%골밀도%원위잡교,형광%토%골형성단백2
leptin%cerebrospinal fluid%tibial fracture%fracture healing%bone density%in siut hybridization,fluores-cence%rabbits%bone morphogenetic protein 2
目的:观察兔胫腓骨骨缺损模型脑室内注射瘦素蛋白(leptin)对骨折愈合速度的影响。方法建立新西兰兔右侧胫腓骨外侧骨缺损模型,leptin组经兔枕骨大孔向小脑延髓池脑脊液中注射重组兔leptin,对照组以相同方法注射等剂量生理盐水。于术后1、3、7、14、21 d记录兔体质量变化,并通过CT动态记录骨缺损区域骨痂骨密度(BMD)的变化。于术后21 d,所有动物均处死后取右侧胫腓骨骨缺损区域,以荧光原位杂交技术(FISH)检测骨折区域骨形成蛋白(BMP)-2的表达情况。结果2组动物造模后,体质量先下降后(14 d)上升,BMD一直呈上升趋势;术后1、3 d,2组体质量及BMD差异均无统计学意义,术后7、14、21 d,leptin组的体质量低于对照组,BMD高于对照组(均P<0.05)。术后21 d,骨缺损区域BMP-2表达阳性细胞数目高于对照组(个:120.87±29.14 vs 97.65±20.97, t=6.79, P<0.001)。结论经枕骨大孔向小脑延髓池内中注射leptin可加速兔四肢骨缺损的愈合。
目的:觀察兔脛腓骨骨缺損模型腦室內註射瘦素蛋白(leptin)對骨摺愈閤速度的影響。方法建立新西蘭兔右側脛腓骨外側骨缺損模型,leptin組經兔枕骨大孔嚮小腦延髓池腦脊液中註射重組兔leptin,對照組以相同方法註射等劑量生理鹽水。于術後1、3、7、14、21 d記錄兔體質量變化,併通過CT動態記錄骨缺損區域骨痂骨密度(BMD)的變化。于術後21 d,所有動物均處死後取右側脛腓骨骨缺損區域,以熒光原位雜交技術(FISH)檢測骨摺區域骨形成蛋白(BMP)-2的錶達情況。結果2組動物造模後,體質量先下降後(14 d)上升,BMD一直呈上升趨勢;術後1、3 d,2組體質量及BMD差異均無統計學意義,術後7、14、21 d,leptin組的體質量低于對照組,BMD高于對照組(均P<0.05)。術後21 d,骨缺損區域BMP-2錶達暘性細胞數目高于對照組(箇:120.87±29.14 vs 97.65±20.97, t=6.79, P<0.001)。結論經枕骨大孔嚮小腦延髓池內中註射leptin可加速兔四肢骨缺損的愈閤。
목적:관찰토경비골골결손모형뇌실내주사수소단백(leptin)대골절유합속도적영향。방법건립신서란토우측경비골외측골결손모형,leptin조경토침골대공향소뇌연수지뇌척액중주사중조토leptin,대조조이상동방법주사등제량생리염수。우술후1、3、7、14、21 d기록토체질량변화,병통과CT동태기록골결손구역골가골밀도(BMD)적변화。우술후21 d,소유동물균처사후취우측경비골골결손구역,이형광원위잡교기술(FISH)검측골절구역골형성단백(BMP)-2적표체정황。결과2조동물조모후,체질량선하강후(14 d)상승,BMD일직정상승추세;술후1、3 d,2조체질량급BMD차이균무통계학의의,술후7、14、21 d,leptin조적체질량저우대조조,BMD고우대조조(균P<0.05)。술후21 d,골결손구역BMP-2표체양성세포수목고우대조조(개:120.87±29.14 vs 97.65±20.97, t=6.79, P<0.001)。결론경침골대공향소뇌연수지내중주사leptin가가속토사지골결손적유합。
Objective To investigate the enhanced osteogenesis during bone fracture healing after intracerebroven-tricular (ICV) leptin injection, using rabbit model with created segmental bone defect in right tibial. Method Segmental critical-sized defects were created at the right tibial bone of skeletally mature New Zealand white rabbits. In experiment group (leptin group), recombinant rabbit leptin was injected into cerebellomedullary cistern through foramen magnum. While in control group, normal saline was injected in the same way. Bone Mineral Density (BMD) was evaluated by qCT at 1st, 3rd, 7th, 14th and the 21st days. At the 21st days, all rabbits were euthanized to collect the right tibia for histomorphology, to ex-amine the BMP-2 expression in the bone callus by Fluorescence in situ hybridization (FISH). Result In the leptin group, body weight declined more obviously than control group then it start to arise at the 14th day;qCT showed significant higher BMD in leptin group than in control group at the 7th day;FISH showed a higher BMP-2 expression in leptin group than in control group. Conclusion Cerebellomedullary leptin injection through foramen magnum could accelerate limb fracture healing in rabbit model with right tibial bone defection.