School of Emergency Management, Jiangsu University, 212000, Zhenjiang, China; School of environment and safety engineering, Jiangsu University, 212000, Zhenjiang, China.
Biofuels Institute of Jiangsu university, Jiangsu University, 212000, Zhenjiang, China; School of environment and safety engineering, Jiangsu University, 212000, Zhenjiang, China.
Environ Pollut. 2024 Mar 1;344:123313. doi: 10.1016/j.envpol.2024.123313. Epub 2024 Jan 5.
Temperature is one of the possible activators for asthma. As global warming continues, the health hazard of high temperatures is increasing. It is unclear, nevertheless, how high temperatures affect asthma. The research aims to examine how asthma is affected by high temperatures and underlying molecular mechanisms. The BALB/c mice were adopted in a model of asthma. The mice were exposed at 24 °C, 38 °C and 40 °C for 4h on weekdays from day 1 to day 30. After the experiment, the lung function was measured in vivo, and then serum protein, pulmonary inflammation and immunohistochemistry assay was assessed in vitro. As the temperature increased from 24 °C to 40 °C, there was a significant increase in serum protein, while there is no discernible difference in serum protein of OVA-sIgE and OVA-sIgG between the OVA (38 °C) group and OVA (24 °C) group. The immunohistochemistry assay showed a change in the pro-inflammatory cytokines. The histopathological analysis exhibited the change of airway structure after high-temperature exposure, especially for exposure at 40 °C. The results of signals protein showed a remarkable rise of TRPV1 for OVA+40 °C. Our results revealed that high temperatures may make asthmatic airway dysfunction severe, and the higher the temperature, the more serious asthma. The oxidative stress and TRPV1 receptor can be a potential drug target for asthma. It will provide a new tool for precision medicine in asthma.
温度是哮喘的可能激活剂之一。随着全球变暖的持续,高温对健康的危害正在增加。然而,高温如何影响哮喘尚不清楚。本研究旨在探讨高温如何影响哮喘以及潜在的分子机制。采用 BALB/c 小鼠建立哮喘模型。在工作日的第 1 天至第 30 天,将小鼠暴露于 24°C、38°C 和 40°C 下 4 小时。实验结束后,在体内测量肺功能,然后在体外评估血清蛋白、肺炎症和免疫组织化学测定。随着温度从 24°C 升高到 40°C,血清蛋白显著增加,而 OVA(38°C)组和 OVA(24°C)组之间 OVA-sIgE 和 OVA-sIgG 的血清蛋白没有明显差异。免疫组织化学测定显示促炎细胞因子发生变化。组织病理学分析显示高温暴露后气道结构发生变化,尤其是暴露于 40°C 时。信号蛋白的结果显示 TRPV1 在 OVA+40°C 时显著升高。我们的结果表明,高温可能使哮喘气道功能障碍加重,温度越高,哮喘越严重。氧化应激和 TRPV1 受体可能成为哮喘的潜在药物靶点。它将为哮喘的精准医学提供新的工具。