医学临床研究
醫學臨床研究
의학림상연구
JOURNAL OF CLINICAL RESEARCH
2014年
1期
14-17,18
,共5页
曹国良%冯月英%施惠华%戴蓉芳%王传慧%凌丹芸
曹國良%馮月英%施惠華%戴蓉芳%王傳慧%凌丹蕓
조국량%풍월영%시혜화%대용방%왕전혜%릉단예
动脉粥样硬化%C反应蛋白质%内皮缩血管肽1%兔
動脈粥樣硬化%C反應蛋白質%內皮縮血管肽1%兔
동맥죽양경화%C반응단백질%내피축혈관태1%토
Atherosclerosis%C-Reactive Protein%Endothelin-1%Rabbits
[目的]观察由内皮素1激活的内皮素A受体对家兔动脉粥样硬化斑块C反应蛋白表达的影响。[方法]32只雄性新西兰大白兔完全随机设计分成基础组、模型组、BQ-123组以及辛伐他汀组,每组8只。饲喂10周后,采耳动脉血检测血清总胆固醇(TC)、三酰甘油(TG)、高密度脂蛋白胆固醇(HDL-C)以及低密度脂蛋白胆固醇(LDL-C)水平;采用免疫组织化学SP法检测主动脉标本中组织内皮素1(ET-1)、巨噬细胞及C反应蛋白(CRP)表达。[结果]模型组、BQ-123组及辛伐他汀组血清 TC、TG、LDL-C均高于基础组( P均<0.01)。BQ-123组及辛伐他汀组血清TC、TG、LDL-C均低于模型组( P均<0.01)。模型组、BQ-123组及辛伐他汀组血清HDL-C低于基础组( P均<0.01)。BQ-123组及辛伐他汀组血清HDL-C高于模型组( P均<0.01)。BQ-123组及辛伐他汀组家兔动脉粥样硬化斑块ET-1、巨噬细胞源泡沫细胞、CRP阳性表达均较模型组明显降低,BQ-123组家兔动脉粥样硬化斑块ET-1、巨噬细胞源泡沫细胞、CRP阳性表达又较辛伐他汀组进一步降低。[结论]ET-1激活的ET受体A(ETRA)可以导致家兔动脉粥样硬化斑块CRP表达的上调;选择性ETRA拮抗剂(ETRAA)可以预防家兔动脉粥样硬化进程的发展。
[目的]觀察由內皮素1激活的內皮素A受體對傢兔動脈粥樣硬化斑塊C反應蛋白錶達的影響。[方法]32隻雄性新西蘭大白兔完全隨機設計分成基礎組、模型組、BQ-123組以及辛伐他汀組,每組8隻。飼餵10週後,採耳動脈血檢測血清總膽固醇(TC)、三酰甘油(TG)、高密度脂蛋白膽固醇(HDL-C)以及低密度脂蛋白膽固醇(LDL-C)水平;採用免疫組織化學SP法檢測主動脈標本中組織內皮素1(ET-1)、巨噬細胞及C反應蛋白(CRP)錶達。[結果]模型組、BQ-123組及辛伐他汀組血清 TC、TG、LDL-C均高于基礎組( P均<0.01)。BQ-123組及辛伐他汀組血清TC、TG、LDL-C均低于模型組( P均<0.01)。模型組、BQ-123組及辛伐他汀組血清HDL-C低于基礎組( P均<0.01)。BQ-123組及辛伐他汀組血清HDL-C高于模型組( P均<0.01)。BQ-123組及辛伐他汀組傢兔動脈粥樣硬化斑塊ET-1、巨噬細胞源泡沫細胞、CRP暘性錶達均較模型組明顯降低,BQ-123組傢兔動脈粥樣硬化斑塊ET-1、巨噬細胞源泡沫細胞、CRP暘性錶達又較辛伐他汀組進一步降低。[結論]ET-1激活的ET受體A(ETRA)可以導緻傢兔動脈粥樣硬化斑塊CRP錶達的上調;選擇性ETRA拮抗劑(ETRAA)可以預防傢兔動脈粥樣硬化進程的髮展。
[목적]관찰유내피소1격활적내피소A수체대가토동맥죽양경화반괴C반응단백표체적영향。[방법]32지웅성신서란대백토완전수궤설계분성기출조、모형조、BQ-123조이급신벌타정조,매조8지。사위10주후,채이동맥혈검측혈청총담고순(TC)、삼선감유(TG)、고밀도지단백담고순(HDL-C)이급저밀도지단백담고순(LDL-C)수평;채용면역조직화학SP법검측주동맥표본중조직내피소1(ET-1)、거서세포급C반응단백(CRP)표체。[결과]모형조、BQ-123조급신벌타정조혈청 TC、TG、LDL-C균고우기출조( P균<0.01)。BQ-123조급신벌타정조혈청TC、TG、LDL-C균저우모형조( P균<0.01)。모형조、BQ-123조급신벌타정조혈청HDL-C저우기출조( P균<0.01)。BQ-123조급신벌타정조혈청HDL-C고우모형조( P균<0.01)。BQ-123조급신벌타정조가토동맥죽양경화반괴ET-1、거서세포원포말세포、CRP양성표체균교모형조명현강저,BQ-123조가토동맥죽양경화반괴ET-1、거서세포원포말세포、CRP양성표체우교신벌타정조진일보강저。[결론]ET-1격활적ET수체A(ETRA)가이도치가토동맥죽양경화반괴CRP표체적상조;선택성ETRA길항제(ETRAA)가이예방가토동맥죽양경화진정적발전。
[Objective]To observe the effect of endothelin receptor A activated by endothelin-1(ET-1) on the expression of C-reactive protein(CRP) in rabbits with atherosclerotic plaque .[Methods] Thirty-two male New Zealand white rabbits were randomly divided into baseline group ,model group ,BQ-123 group and simv-astatin group with 8 rabbits in each group .After 10 weeks ,the peripheral blood was collected from ear artery to determine the levels of total cholesterol (TC) ,triglyceride(TG) ,high density lipoprotein cholesterol(HDL-C) and low density lipoprotein cholesterol(LDL-C) in serum .SP immunohistochemical staining was used to detect the expression of ET-1 ,macrophage and CRP in aorta .[Results] Serum levels of TC ,TG and LDL-C in model group ,BQ-123 group and simvastatin group were significantly higher than those in baseline group(all P<0 .01) ,while serum levels of TC ,TG and LDL-C in BQ-123 group and simvastatin group were significant-ly lower than those in model group(all P<0 .01) .Serum levels of HDL-C in model group ,BQ-123 group and simvastatin group were significantly lower than those in baseline group (all P<0 .01) .Serum levels of HDL-C in BQ-123 group and simvastatin group were higher than those in model group (all P <0 .01) .Compared with model group ,the positive expression of ET-1 ,macrophage-derived foam cells and CRP in BQ-123 group and simvastatin group decreased obviously .Compared with simvastatin group ,the positive expression of ET-1 , macrophage-derived foam cells and CRP in BQ-123 group further decreased .[Conclusion] Endothelin receptor A activated by ET-1 can up regulate the expression of CRP protein in atherosclerotic plaque of rabbits .Selec-tive endothelin receptor A antagonist can prevent the development of atherosclerosis in rabbits .