中国现代医学杂志
中國現代醫學雜誌
중국현대의학잡지
CHINA JOURNAL OF MODERN MEDICINE
2004年
23期
9-13
,共5页
唐艺加%黄晶%王新%张俊霞%唐海林%刘地川%邓昌明%刘光聪%吕基全
唐藝加%黃晶%王新%張俊霞%唐海林%劉地川%鄧昌明%劉光聰%呂基全
당예가%황정%왕신%장준하%당해림%류지천%산창명%류광총%려기전
动脉损伤%超声辐照%再狭窄%分子机制
動脈損傷%超聲輻照%再狹窄%分子機製
동맥손상%초성복조%재협착%분자궤제
artery lesions%USE%restenosis%molecular mechanisms
目的探讨超声辐照抗再狭窄作用的分子机制.方法建立大鼠颈动脉球囊损伤模型,予血管外超声辐照,采用原位杂交与免疫组化技术分别于术后30 min与4 h对血管壁-jun,hsp70,BAX(仅行免疫组化)的表达进行检测,对上述指标在术后以及超声辐照后的表达变化情况进行比较.结果原位杂交显示球囊损伤后30min-jun与hsp70 mRNA的表达显著增强,超声辐照降低了hsp70 mRNA在术后30 min的高表达(P<0.01),对c-jun mRNA的表达无显著影响(P=0.773);术后4 h免疫组化结果与原位杂交结果基本吻合,同时发现超声辐照增强了术后4 h BAX蛋白在动脉壁中的表达(P<0.05).结论该参数超声辐照减轻动脉损伤后再狭窄的作用机制可能与其在动脉损伤后早期减少hsp70的表达及增强BAX的表达有关,而与术后早期c-jun的高表达无明显关系.
目的探討超聲輻照抗再狹窄作用的分子機製.方法建立大鼠頸動脈毬囊損傷模型,予血管外超聲輻照,採用原位雜交與免疫組化技術分彆于術後30 min與4 h對血管壁-jun,hsp70,BAX(僅行免疫組化)的錶達進行檢測,對上述指標在術後以及超聲輻照後的錶達變化情況進行比較.結果原位雜交顯示毬囊損傷後30min-jun與hsp70 mRNA的錶達顯著增彊,超聲輻照降低瞭hsp70 mRNA在術後30 min的高錶達(P<0.01),對c-jun mRNA的錶達無顯著影響(P=0.773);術後4 h免疫組化結果與原位雜交結果基本吻閤,同時髮現超聲輻照增彊瞭術後4 h BAX蛋白在動脈壁中的錶達(P<0.05).結論該參數超聲輻照減輕動脈損傷後再狹窄的作用機製可能與其在動脈損傷後早期減少hsp70的錶達及增彊BAX的錶達有關,而與術後早期c-jun的高錶達無明顯關繫.
목적탐토초성복조항재협착작용적분자궤제.방법건립대서경동맥구낭손상모형,여혈관외초성복조,채용원위잡교여면역조화기술분별우술후30 min여4 h대혈관벽-jun,hsp70,BAX(부행면역조화)적표체진행검측,대상술지표재술후이급초성복조후적표체변화정황진행비교.결과원위잡교현시구낭손상후30min-jun여hsp70 mRNA적표체현저증강,초성복조강저료hsp70 mRNA재술후30 min적고표체(P<0.01),대c-jun mRNA적표체무현저영향(P=0.773);술후4 h면역조화결과여원위잡교결과기본문합,동시발현초성복조증강료술후4 h BAX단백재동맥벽중적표체(P<0.05).결론해삼수초성복조감경동맥손상후재협착적작용궤제가능여기재동맥손상후조기감소hsp70적표체급증강BAX적표체유관,이여술후조기c-jun적고표체무명현관계.
Objective: To investigate the molecular mechanisms of the anti-restenosis effects of ultrasound exposure (USE). Methods: Balloon injured model of carotid artery of rats had been built with a 2F balloon catheter, then USE (705KHz, 1 w/cm2, 3 min) was applied. The expression of c-jun, hsp70 and BAX in the artery wall was detected by in situ hybridization (ISH) and Immunohistochemistry (IHC) 30 minutes and 4 hours after balloon lesions respectively. Results: The expression of c-jun and hsp70 mRNA in normal carotid artery increased significantly 30minutes after balloon lesions. There was no difference of c-jun mRNA expression between Balloon and Balloon+USE group (P =0.773), but the expression of hsp70 mRNA was significantly lower in the latter group (P <0.01). Results of the later IHC were similar with that of the ISH detection. The expression of BAX protein was significantly higher in Balloon+USE group than in Normal group (P <0.01) and Balloon group (P <0.05). USE alone couldn't change the expression of hsp70 and c-jun compared with Normal group. Conclusion: The anti-restenosis effects of the USE might be related to the changed expression of hsp70 and BAX in the damaged artery wall.