College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.
College of Medical Laboratory Technology, Zhengzhou University, Zhengzhou, Henan, China.
Environ Toxicol. 2020 Aug;35(8):831-839. doi: 10.1002/tox.22919. Epub 2020 Mar 13.
Glyburide is a classic antidiabetic drug that is dominant in inflammation regulation, but its specific role in ozone-induced lung inflammation and injury remains unclear. In order to investigate whether glyburide prevents ozone-induced pulmonary inflammation and its mechanism, C57BL/6 mice were intratracheally pre-instilled with glyburide or the vehicle 1 hour before ozone (1 ppm, 3 hours) or filtered air exposure. After 24 hours, the total inflammatory cells and total protein in bronchoalveolar lavage fluid (BALF) were detected. The pathological alternations in lung tissues were evaluated by HE staining. The expression of NLRP3, interleukin-1β (IL-1β), and IL-18 protein in lung tissues was detected by immunohistochemistry. Western blotting was used to examine the levels of caspase-1 p10 and active IL-1β protein. Levels of IL-1β and IL-18 in BALF were measured using ELISA kits. Glyburide treatment decreased the total cells in BALF, the inflammatory score, and the mean linear intercept induced by ozone in lung tissues. In addition, glyburide inhibited the expression of NLRP3, IL-18, and IL-1β protein in lung tissues, and also suppressed NLRP3 inflammasome activation, including caspase-1 p10, active IL-1β protein in lung tissues, IL-1β, and IL-18 in BALF. These results demonstrate that glyburide effectively attenuates ozone-induced pulmonary inflammation and injury via blocking the NLRP3 inflammasome.
格列吡嗪是一种经典的抗糖尿病药物,在炎症调节中占主导地位,但它在臭氧诱导的肺炎症和损伤中的具体作用尚不清楚。为了研究格列吡嗪是否预防臭氧诱导的肺炎症及其机制,C57BL/6 小鼠在臭氧(1 ppm,3 小时)或过滤空气暴露前 1 小时通过气管内预注入格列吡嗪或载体。24 小时后,检测支气管肺泡灌洗液(BALF)中的总炎性细胞和总蛋白。通过 HE 染色评估肺组织的病理改变。通过免疫组织化学检测肺组织中 NLRP3、白细胞介素-1β(IL-1β)和白细胞介素-18 蛋白的表达。Western blot 用于检测半胱天冬酶-1 p10 和活性 IL-1β 蛋白的水平。使用 ELISA 试剂盒测量 BALF 中的 IL-1β 和 IL-18 水平。格列吡嗪治疗降低了臭氧诱导的 BALF 中总细胞、炎症评分和肺组织中的平均线性截距。此外,格列吡嗪抑制了肺组织中 NLRP3、IL-18 和 IL-1β 蛋白的表达,并抑制了 NLRP3 炎性小体的激活,包括肺组织中的半胱天冬酶-1 p10、活性 IL-1β 蛋白、BALF 中的 IL-1β 和 IL-18。这些结果表明,格列吡嗪通过阻断 NLRP3 炎性小体有效减轻臭氧诱导的肺炎症和损伤。