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I 型血管紧张素受体拮抗剂坎地沙坦和厄贝沙坦对过敏性哮喘的抑制作用。

Suppressive effects of type I angiotensin receptor antagonists, candesartan and irbesartan on allergic asthma.

机构信息

College of Pharmacy, Pusan National University, Busan 46241, Republic of Korea.

College of Pharmacy, Pusan National University, Busan 46241, Republic of Korea.

出版信息

Eur J Pharmacol. 2019 Jun 5;852:25-33. doi: 10.1016/j.ejphar.2019.02.035. Epub 2019 Feb 21.

Abstract

The effects of candesartan and irbesartan, antagonists of the type I angiotensin II receptor, were investigated on allergic asthma. The antigen-induced degranulation was measured by evaluating β-hexosaminidase activity in vitro. Additionally, a murine ovalbumin-induced allergic asthma model was used to test the in vivo efficacy. It was observed that while candesartan inhibited the antigen-induced degranulation in rat RBL-2H3 mast cells, irbesartan did not. Administration of candesartan and irbesartan decreased the number of immune cells in the bronchoalveolar lavage fluid and reduced the expression of Th2 (IL-4, IL-5, and IL-13) and Th1 cytokines (IL-2 and IFN-γ) in the lung tissues of mice with ovalbumin-induced allergic asthma. Histological studies revealed that both antagonists reduced inflammation and mucin production in the lungs. Therefore, these findings provide evidence that candesartan and irbesartan could have potential applications as anti-allergic agents.

摘要

我们研究了血管紧张素Ⅱ受体Ⅰ型拮抗剂坎地沙坦和厄贝沙坦对过敏性哮喘的作用。通过体外测定β-己糖胺酶活性来检测抗原诱导的脱颗粒作用。此外,还使用了一种小鼠卵清蛋白诱导的过敏性哮喘模型来测试体内疗效。结果表明,坎地沙坦抑制了大鼠 RBL-2H3 肥大细胞的抗原诱导脱颗粒,而厄贝沙坦则没有。坎地沙坦和厄贝沙坦的给药减少了支气管肺泡灌洗液中的免疫细胞数量,并降低了卵清蛋白诱导的过敏性哮喘小鼠肺组织中 Th2(IL-4、IL-5 和 IL-13)和 Th1 细胞因子(IL-2 和 IFN-γ)的表达。组织学研究表明,这两种拮抗剂均减轻了肺部的炎症和粘蛋白产生。因此,这些发现为坎地沙坦和厄贝沙坦作为抗过敏药物具有潜在应用提供了证据。

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