山东医药
山東醫藥
산동의약
SHANDONG MEDICAL JOURNAL
2015年
14期
16-18
,共3页
韦肖敏%覃晓%卢海林%蒋汶洪
韋肖敏%覃曉%盧海林%蔣汶洪
위초민%담효%로해림%장문홍
动脉钙化,大鼠%基质金属蛋白酶%转化生长因子β
動脈鈣化,大鼠%基質金屬蛋白酶%轉化生長因子β
동맥개화,대서%기질금속단백매%전화생장인자β
arterial calcification%matrix metalloproteinases%matrix metalloproteinases-9%transforming growth factor-β
目的:探讨转化生长因子β( TGF-β)和基质金属蛋白酶( MMPs)在动脉钙化发生、发展中的作用。方法60只雄性SD大鼠随机分为实验组和对照组各30只。实验组连续3d皮下注射维生素D3注射液50万U/( kg· d)制备动脉钙化模型,对照组同时注射等量葡萄糖注射液。两组同时间皮下注射同等剂量的不含维生素D3的5%葡萄糖注射液。采用Von Kossa 染色法观察动脉钙化程度;实时荧光定量PCR 法测定动脉组织 TGF-βmRNA和MMPs mRNA表达量。结果实验组动脉钙化程度、TGF-βmRNA和MMPs mRNA表达量均明显高于对照组(P均<0.05)。结论 TGF-β和MMPs可促进动脉硬化的形成。
目的:探討轉化生長因子β( TGF-β)和基質金屬蛋白酶( MMPs)在動脈鈣化髮生、髮展中的作用。方法60隻雄性SD大鼠隨機分為實驗組和對照組各30隻。實驗組連續3d皮下註射維生素D3註射液50萬U/( kg· d)製備動脈鈣化模型,對照組同時註射等量葡萄糖註射液。兩組同時間皮下註射同等劑量的不含維生素D3的5%葡萄糖註射液。採用Von Kossa 染色法觀察動脈鈣化程度;實時熒光定量PCR 法測定動脈組織 TGF-βmRNA和MMPs mRNA錶達量。結果實驗組動脈鈣化程度、TGF-βmRNA和MMPs mRNA錶達量均明顯高于對照組(P均<0.05)。結論 TGF-β和MMPs可促進動脈硬化的形成。
목적:탐토전화생장인자β( TGF-β)화기질금속단백매( MMPs)재동맥개화발생、발전중적작용。방법60지웅성SD대서수궤분위실험조화대조조각30지。실험조련속3d피하주사유생소D3주사액50만U/( kg· d)제비동맥개화모형,대조조동시주사등량포도당주사액。량조동시간피하주사동등제량적불함유생소D3적5%포도당주사액。채용Von Kossa 염색법관찰동맥개화정도;실시형광정량PCR 법측정동맥조직 TGF-βmRNA화MMPs mRNA표체량。결과실험조동맥개화정도、TGF-βmRNA화MMPs mRNA표체량균명현고우대조조(P균<0.05)。결론 TGF-β화MMPs가촉진동맥경화적형성。
Objective To explore the potential role of transforming growth factor-β( TGF-β) and matrix metallopro-teinases ( MMPs) in its occurrence and development of arterial calcification .Methods Sixty male SD rats were randomly divided into the control group and experimental group , with 30 rats in each group .Rats in the experimental group were in-jected vitamin D3 with a dose of 500 000 U/( kg· d) subcutaneously for 3 consecutive days , which was in order to induce the arterial calcification in rat models .The same dose of 5% glucose without vitamin D3 was injected into the rats of two groups subcutaneously .Using Von Kossa staining to observe the degree of tissue calcification of the rats , and using real-time fluorescent quantitative PCR to determinate the expression of mRNA of TGF-βand MMPs in the two groups .Results The degree of calcification and the mRNA expression of TGF-βand MMPs in the experimental group were significantly higher than those of the control group (all P<0.05).Conclusion The TGF-βand MMPs may contribute to the formation of arterial calcification .