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首页> 外文期刊>Heart and vessels: An international journal >The effect of Telmisartan on the expression of connexin43 and neointimal hyperplasia in a rabbit iliac artery restenosis model
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The effect of Telmisartan on the expression of connexin43 and neointimal hyperplasia in a rabbit iliac artery restenosis model

机译:替米沙坦的表达的影响connexin43和新生内膜增生一只兔子髂动脉再狭窄模型

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We established a rabbit iliac artery restenosis model to explore the impact of Telmisartan on the expression of Connexin43 (Cx43) and neointimal hyperplasia. Thirty New Zealand white rabbits were randomly divided into three groups: control group (n = 10), restenosis group (n = 10), and Telmisartan group (n = 10). The restenosis model was established by high-cholesterol diet combined with double-balloon injury of iliac arteries. In addition, Telmisartan at 5 mg/(kg day) was administered to the rabbits of Telmisartan group on the second day after the second balloon injury. All rabbits were killed at the end of the experiment followed by institution policy. Before sacrifice, blood samples were obtained to test serum angiotensinII (AngII). Iliac arteries were isolated for morphological analysis and determining the expression of Cx43 by HE staining, immunohistochemical analysis, reverse transcription-polymerase chain reaction (RT-PCR), and Western Blotting analysis. Then, the local AngII levels of arteries were measured by radioimmunoassay. As compared with controls, the expression of Cx43 mRNA (0.98 +/- 0.08) vs. (1.27 +/- 0.17), P < 0.01), and Cx43 protein [(0.75 +/- 0.08) vs. (0.90 +/- 0.08), P < 0.05] of restenosis group were increased, which were significantly higher than those of Telmisartan group [Cx43 mRNA: (1.27 +/- 0.17) vs. (1.00 +/- 0.20), P < 0.01; Cx43 protein: (0.90 +/- 0.08) vs. (0.82 +/- 0.05), P < 0.05]. Furthermore, The intima thickness [(266.12 +/- 70.27) vs. (2.85 +/- 0.19) mu m, P < 0.01] and the local AngII [(115.6 +/- 15.7) vs. (90.1 +/- 7.7), P < 0.05] of restenosis group were raised when compared with controls. Telmisartan group exhibited thinner intima compared with restenosis group [(68.22 +/- 24.37) vs. (266.12 +/- 70.27), P < 0.01]. However, the local AngII levels between these two groups were approximate. In addition, the plasma concentration of AngII was not significantly different among three groups. In conclusion, Telmisartan can inhibit the expression of connexin43 and neointimal hyperplasia in iliac artery restenosis model.
机译:我们建立了一个兔髂动脉再狭窄模型探讨替米沙坦的影响表达Connexin43 (Cx43)和血管内膜增生。被随机分为三组:控制组(n = 10)、再狭窄组(n = 10)替米沙坦组(n = 10)。建立了高胆固醇饮食相结合与双气囊髂动脉的损伤。另外,替米沙坦在5毫克/(公斤)管理的兔子替米沙坦组第二天在第二次气球受伤。实验机构政策紧随其后。牺牲,血样测试获得的血清angiotensinII (AngII)。孤立的形态分析和由他决定Cx43表达的染色、免疫组织化学分析、逆转聚合酶链反应(rt - pcr),和免疫印迹分析。AngII动脉测量的水平放射免疫检定法。Cx43 mRNA的表达(0.98 + / - 0.08)和(1.27+ / - 0.17), P < 0.01),和Cx43蛋白[(0.75 + / -0.08)和(0.90 + / - 0.08),P < 0.05)再狭窄组增加,显著高于替米沙坦集团(Cx43 mRNA:(1.27 + / - 0.17)和(1.00 + / -0.20), P < 0.01;与(0.82 + / - 0.05),P < 0.05)。内膜厚度((266.12 + / - 70.27)和(2.85+ / - 0.19μm, P < 0.01)和当地AngII[6(115 + / - 15℃。)美国(90 + / - 7。7),P < 0.05]的再狭窄组相比与控制。薄内膜与再狭窄组[(+ / - 24.37 68.22) vs (+ / - 70.27 266.12), P <0.01]。这两组近似。AngII不是的血浆浓度在三组明显不同。结论替米沙坦可以抑制connexin43的表达和血管内膜增生在髂动脉再狭窄模型。

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