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Effects of angiotensin Ⅱ receptor antagonist on expression of collagen Ⅲ, collagen Ⅴ , and transforming growth factor β_1 in the airway walls of sensitized rats

机译:血管紧张素Ⅱ受体拮抗剂对致敏大鼠气道壁Ⅲ型,Ⅴ型胶原及转化生长因子β_1表达的影响。

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Background Repeated attacks of bronchial asthma lead to different degrees of airway remodeling, the mechanism of which is not yet clear. Some evidences indicate that it is related to the excessive expression of some growth promotion factors. Angiotensin Ⅱ is a polypeptide that may be involved in airway remodeling. To evaluate its role in airway remodeling in asthma, we observed the effects of an angiotensin Ⅱ type 1 receptor antagonist (valsartan) on the expression of collagen Ⅲ, collagen Ⅴ, and transforming growth factor β_1 (TGF-β_1) mRNA and protein in the airway walls of sensitized rats. Methods Forty Wistar rats were randomly divided into 5 groups: control group, sensitized group, and valsartan groups 1, 2, and 3. The rats in the sensitized group and in valsartan groups 1, 2, and 3 were sensitized and challenged with ovalbumin. Rats in control group were sensitized and challenged with 0. 9% NaCl. Rats from valsartan groups 1,2, and 3 were drenched with valsartan (10 μg, 20 μg, or 30 μg, respectively) at the time of the ovalbumin challenges. The expression of collagen Ⅲ, collagen Ⅴ, and TGF-β_1 protein were detected using immunohistochemical method in combination with image analysis methods. The expression of TGF-耞1 mRNA was detected by in situ hybridization. Results The expression in the airways of collagen Ⅲ and collagen Ⅴ was significantly higher in rats from the sensitized group (7.73 +- 0. 81, 1.34 +- 0.28) and from valsartan groups 1, 2, and 3 (5. 73 +- 0. 64, 1.13 +- 0.15; 4. 96 +- 0. 51, 0. 98 +- 0. 08; 4. 43 +- 0. 35, 0. 93 +- 0. 06, respectively) than those in the control group (2. 65 +- 0. 38, 0. 67 +- 0. 08, P < 0. 05 ). In addition, collagen levels were significantly lower in valsartan groups 1, 2, and 3 than those from the sensitized group (P<0. 05). The expression of TGF-β_1 mRNA and protein in the airways was significantly higher in rats from the sensitized group (20.49% +- 3.46%, 29.73% +- 3.25%) and from valsartan groups 1, 2, and 3 (16. 47% +- 1. 94% , 19.41% +- 1. 87%; 14. 38% +- 1. 58% , 18. 29% +- 1. 43% ; 12. 96% +- 1. 73% , 18. 63% +- 1.11%, respectively) than that from the control group (7.84% +- 1.61%, 5.63% +- 1. 07%, P<0. 05). TGF-β_1 mRNA and protein levels were significantly lower in valsartan groups 1, 2. and 3 than that in the sensitized group (P<0. 05). Conclusions Angiotensin Ⅱ receptor antagonist valsartan can suppress synthesis of collagen Ⅲ and collagen Ⅴ by downregulating TGF-β_1 mRNA and protein expression. Valsartan can decrease airway remodeling and could play a role in asthma therapy.
机译:背景支气管哮喘反复发作导致不同程度的气道重塑,其机制尚不清楚。一些证据表明,这与某些促进生长因子的过度表达有关。血管紧张素Ⅱ是一种可能与气道重塑有关的多肽。为了评估其在哮喘气道重塑中的作用,我们观察了血管紧张素Ⅱ1型受体拮抗剂(缬沙坦)对血管紧张素Ⅲ,胶原Ⅴ和转化生长因子β_1(TGF-β_1)mRNA和蛋白表达的影响。致敏大鼠的气道壁。方法40只Wistar大鼠随机分为5组:对照组,致敏组和缬沙坦1、2、3组。分别对致敏组和缬沙坦1、2、3组的大鼠进行卵清蛋白致敏和攻击。对照组的大鼠致敏并用0. 9%NaCl激发。在卵清蛋白激发时,用缬沙坦(分别为10μg,20μg或30μg)浸湿来自valsartan组1,2和3的大鼠。免疫组织化学结合图像分析方法检测Ⅲ型胶原,Ⅴ型胶原和TGF-β_1蛋白的表达。通过原位杂交检测TGF-β1mRNA的表达。结果致敏组(7.73 +-0. 81,1.34 +-0.28)和缬沙坦1、2和3组(5. 73 +-)的大鼠中,Ⅲ型胶原和Ⅴ型胶原在气道中的表达明显升高。 0. 64,1.13 +-0.15; 4. 96 +-0. 51,0. 98 +/- 0. 08; 4. 43 +/- 0. 35,0. 93 +/- 0. 06)对照组(2. 65 +-0. 38,0. 67 +-0. 08,P <0. 05)。此外,缬沙坦1、2和3组的胶原蛋白水平明显低于致敏组(P <0。05)。致敏组(20.49%+-3.46%,29.73%+-3.25%)和缬沙坦1、2和3组(16. 47)的大鼠气道中TGF-β_1mRNA和蛋白的表达明显更高。 %+1。94%,19.41%+1。87%; 14. 38%+1。58%,18. 29%+1。43%; 12. 96%+1。73%,分别比对照组的18. 63%±1.11%(7.84%±1.61%,5.63%±1.0%,P <0。05)。缬沙坦1、2和3组的TGF-β_1mRNA和蛋白质水平明显低于致敏组(P <0。05)。结论血管紧张素Ⅱ受体拮抗剂缬沙坦通过下调TGF-β_1mRNA和蛋白表达抑制Ⅲ型和Ⅴ型胶原的合成。缬沙坦可以减少气道重塑,并可能在哮喘治疗中发挥作用。

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