当归对大鼠心肌缺血/再灌注损伤蛋白激酶C的影响  被引量:12

Effect of angelica on protein kinase C during myocardial ischemia reperfusion injury in rat

在线阅读下载全文

作  者:王焱林[1] 王成夭[1] 曾锐[1] 陈锋[1] 万德宁[1] 

机构地区:[1]湖北医科大学附属第二医院麻醉科,武汉市430071

出  处:《中华麻醉学杂志》2000年第8期490-492,共3页Chinese Journal of Anesthesiology

摘  要:目的 目的研究当归抗心肌缺血 /再灌注损伤的分子生物学机制。方法 结扎 /开放左冠状动脉前降支结扎 40min/开放 12 0min建立心肌缺血 /再灌注模型。选用SD大鼠 40只 ,随机分成三组 :对照组 (A组 ,n =10只 ) ,丝线穿过冠状动脉前降支但不结扎 ;缺血 /再灌注组 (B组 ,n =15只 ) ,缺血 /再灌注前舌静脉注射生理盐水 0 8ml/ 10 0 g ,当归治疗组 (C组 ,n =15只 ) ,缺血再灌注前舌静脉注射 2 5 %当归注射液 0 8ml/ 10 0 g。采用免疫组化SP法测定蛋白激酶C(PKC)含量和同位素标记法测定PKC活性。结果 与B组比较 ,C组心肌梗死面积显著缩小 (P <0 0 1) ,A组及C组PKC灰度值显著性降低 (P <0 0 1) ,A组PKC的活性无显著性差异 (P >0 0 5 ) ,而C组PKC活性明显升高 (P <0 0 1)。与A组比较 ,C组PKC的灰度值无显著性差异 (P >0 0 5 ) ,PKC的活性明显升高(P <0 0 1)。C组的PKC多分布在细胞膜上 ,A组及B组的PKC多分布在细胞核和细胞浆内。结论 当归可促使PKC从细胞核转移到细胞膜 ,从而激活PKC抑制心肌缺血 /再灌注损伤。Objective To study the molecular biological mechanism of the protective effect of angelica on myocardium during ischemia reperfusion Methods The myocardial ischemia/reperfusion was induced with the 40 min cross clamp/120 min declamping of anterior decending coronary artery Forty SD rats were randomly divided into 3 groups: group A without myocardial ischemic reperfusion , group B with intravenous adminisrtration of normal saline 0 8ml/100g before ischemia reperfusion , and group C with intravenous adminisrtration of 25% angelica 0 8ml/100g before ischemia reperfusion The content of protein kinase C (PKC) in cardiac myocyte was measured with immunohistochemical method, and the PKC activity with the isotope lable method Results Compared with those in group B, the myocardial infarct size reduced significantly in group C (P<0 01), the grey value of PKC decreased markedly in group A or C(P<0 01),the PKC activity remained unsignificant change in group A (P>0 05) but increased obviously in group C (P<0 01) There was not significant difference in the grey value of PKC between group C and A (P>0 05) The PKC activity was significantly higher in group C than that in group A(P<0 01) PKC was located at cellular membrane in group C, but at cellular nucleus or in cellular plasm in groups A and B Conclusions Angelica can protect myocardium from ischemia reperfusion injury through activation of PKC by impelling PKC to transfer from cellular nucleus or cellular plasm to cellular membrane

关 键 词:当归 心肌缺血 实验研究 蛋白激酶C 

分 类 号:R285.5[医药卫生—中药学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象