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重庆三峡医药高等专科学校
纸质出版日期:2016,
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[1]付海荣.硫酸锌联合阿司匹林对大鼠急性心肌梗死的保护作用及机制研究[J].重庆医科大学学报,2016,41(12):1204-1209.
Fu Hairong. Protection and mechanism of zinc sulfate combined with aspirin for acute myocardial infarction[J]. Journal of Chongqing Medical University, 2016,41(12):1204-1209.
[1]付海荣.硫酸锌联合阿司匹林对大鼠急性心肌梗死的保护作用及机制研究[J].重庆医科大学学报,2016,41(12):1204-1209. DOI: 10.13406/j.cnki.cyxb.001011.
Fu Hairong. Protection and mechanism of zinc sulfate combined with aspirin for acute myocardial infarction[J]. Journal of Chongqing Medical University, 2016,41(12):1204-1209. DOI: 10.13406/j.cnki.cyxb.001011.
目的:探讨硫酸锌联合阿司匹林治疗对大鼠急性心肌梗死的疗效及其机制。方法:选取100只200 g左右的雌性SD大鼠
随机分为5组
每组20只。假手术组不结扎并按常规饮食喂养
其余4组结扎并在常规饮食的基础上分别给以无菌蒸馏水(对照组)、硫酸锌、阿司匹林、硫酸锌联合阿司匹林
连续给药7 d后
使用超声心动图及侵入性导管检测心功能及血流动力学指标
并对大鼠血液中的肌钙蛋白T进行检测
然后取出心脏切片进行HE和Masson染色检验
检测各组心脏组织中的转化生长因子-β1(transforming growth factor-β1
TGF-β1)、环氧合酶-2(cyclooxygenase-2
COX-2)、超氧化物歧化酶1(superoxide dismutase-1
SOD-1)和谷胱甘肽过氧化物酶-4(glutathione peroxidase-4
GPX-4)的m RNA和蛋白质的表达情况。结果:给以阿司匹林和硫酸锌联合阿司匹林均能改善心肌梗死情况
保护受损心肌;与单独使用阿司匹林比较
硫酸锌联合阿司匹林更能显著提高收缩压[(119±11)mm Hg vs.(103±7)mm Hg
P=0.037]、舒张压[(98±4)mm Hg vs.(83±6)mm Hg
P=0.041]、平均动脉压[(103±6)mm Hg vs.(89±5)mm Hg
P=0.029]及Emax[(5.27±0.33)mm Hg/μL vs.(4.13±0.29)mm Hg/μL
P=0.027];降低炎性侵润、心肌梗死面积、心率[(328±11)beats/min vs.(364±19)beats/min
P=0.016]、全身血管阻力[(6.70±0.39)mm Hg×min/μL vs.(8.73±0.59)mm Hg×min/μL
P=0.039]及心肌梗死标志物肌钙蛋白T的水平[(583±51)pg/m L vs.(819±57)pg/m L
P=0.017];同时也更能降低促炎细胞因子TGF-β1和COX-2的m RNA[(0.65±0.18)vs.(1.48±0.12)
P=0.014;(0.70±0.12)vs.(1.21±0.08)
P=0.031]及蛋白[(2.42±0.19)vs.(3.61±0.27)
P=0.032;(1.76±0.32)vs.(5.20±0.59)
P=0.018)]表达水平
增加抗氧化酶SOD-1和GPX-4的m RNA[(2.14±0.11)vs.(1.58±0.12)
P=0.021;(2.69±0.17)vs.(1.87±0.07)
P=0.018]及蛋白[(5.40±0.62)vs.(2.40±0.33)
P=0.036;(4.26±0.47)vs.(2.72±0.51)
P=0.023]表达水平。结论:硫酸锌联合阿司匹林可有效保护急性心肌梗死对心肌的损伤
其主要的作用机制可能是通过抑制促炎细胞因子TGF-β1和COX-2
激活抗氧化酶类SOD-1和GPX-4的水平
实现抗炎抗氧化的作用
从而达到对急性心肌梗死的保护效果。
Objective:To investigate the protection and mechanism of zinc sulfate combined with aspirin for acute myocardial infarction treatment. Methods:Totally 100 female SD rats were selected and randomly divided into five groups
20 rats in each group. The acute myocardial infarction model was established through ligation of the left anterior descending artery(LAD)in all groups except sham group. Different groups were given different agents
namely sterile distilled water
zinc sulfate
aspirin and zinc sulfate combination with aspirin. After 7 days
cardiac function indexes were detected through invasive cather and echocardiogram
and the blood troponin T also was detected. Then all heart tissues were harvested for HE and Masson staining. m RNA and protein expression levels of transforming growth factor-β1(TGF-β1)
cyclooxygenase-2(COX-2)
superoxide dismutase-1(SOD-1) and glutathione peroxidase-4(GPX-4)were also detected. Results:Both aspirin and zinc sulfate combined with aspirin could improve cardiac function. Compared with aspirin alone
zinc sulfate combined with aspirin can significantly increase systolic pressure [(119 ± 11) mm Hg vs.(103 ± 7)mm Hg
P=0.037]
diastolic pressure [(98±4)mm Hg vs.(83±6)mm Hg
P=0.041]
average arterial blood pressure[(103±6)mm Hg vs.(89±5)mm Hg
P=0.029] and Emax[(5.27±0.33)mm Hg/μL vs.(4.13 ± 0.29)mm Hg/μL
P=0.027];decrease inflammatory infiltration and infract size
heart rate [(328 ± 11) beats/min vs.(364±19)beats/min
P=0.016]
systemic vascular resistance[(6.70±0.39)mm Hg×min/μL vs.(8.73±0.59) mm Hg×min/μL
P=0.039]
levels of troponin T[(583±51)pg/m L vs.(819±57)pg/m L
P=0.017]
moreover
levels of m RNA[(0.65 ± 0.18)vs.(1.48±0.12)
P=0.014;(0.70±0.12)vs.(1.21±0.08)
P=0.031] and protein[(2.42±0.19)vs.(3.61±0.27)
P=0.032;(1.76±0.32)vs.(5.20±0.59)
P=0.018)] of pro-inflammatory cytokine TGF-β1 and COX-2;increase the levels of m RNA[(2.14 ± 0.11)vs.(1.58±0.12)
P=0.021;(2.69 ± 0.17)vs.(1.87±0.07)
P=0.018] and protein[(5.40±0.62)vs.(2.40±0.33)
P=0.036;(4.26±0.47)vs.(2.72 ± 0.51)
P=0.023] of antioxidant enzyme SOD-1 and GPX-4. Conclusion:Zinc sulfate combined with aspirin can effectively protect acute myocardial infarction
and the main mechanism is probably through inhibiting pro-inflammatory cytokine TGF-β1 and COX-2
enhancing antioxidant enzymes SOD-1 and GPX-4 to protect acute myocardial infarction.
心肌梗死硫酸锌阿司匹林
myocardial infarctionzinc sulfateaspirin
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