Department of Tropical Medicine, College of Military Preventive Medicine, Army Medical University, Chongqing, China.
Key Laboratory of Extreme Environmental Medicine, Ministry of Education of China, Chongqing, China.
Microb Biotechnol. 2023 Nov;16(11):2114-2130. doi: 10.1111/1751-7915.14349. Epub 2023 Oct 4.
The severity of heat stroke (HS) is associated with intestinal injury, which is generally considered an essential issue for HS. Heat acclimation (HA) is considered the best strategy to protect against HS. In addition, HA has a protective effect on intestinal injuries caused by HS. Considering the essential role of gut microbes in intestinal structure and function, we decided to investigate the potential protective mechanism of HA in reducing intestinal injury caused by HS. HA model was established by male C57BL/6J mice (5-6 weeks old, 17-19 g) were exposed at (34 ± 0.7)°C for 4 weeks to establish an animal HA model. The protective effect of HA on intestinal barrier injury in HS was investigated by 16S rRNA gene sequencing and nontargeted liquid chromatography-mass spectrometry (LC-MS) metabolomics. According to the experimental results, HA can change the composition of the gut microbiota, which increases the proportion of lactobacilli, faecal bacteria, and urinobacteria but decreases the proportion of deoxycholic acid. Moreover, HA can reduce liver and kidney injury and systemic inflammation caused by HS and reduce intestinal injury by enhancing the integrity of the intestinal barrier. In addition, HA regulates inflammation by inhibiting NF-κB signalling and increasing tight junction protein expression in HS mice. HA induces changes in the gut microbiota, which may enhance tight junction protein expression, thereby reducing intestinal inflammation, promoting bile acid metabolism, and ultimately maintaining the integrity of the intestinal barrier. In conclusion, HA induced changes in the gut microbiota. Among the gut microbiota, lactobacilli may play a key role in the potential protective mechanism of HA.
热射病(HS)的严重程度与肠道损伤有关,这通常被认为是 HS 的一个重要问题。热适应(HA)被认为是预防 HS 的最佳策略。此外,HA 对 HS 引起的肠道损伤具有保护作用。考虑到肠道微生物在肠道结构和功能中的重要作用,我们决定研究 HA 减轻 HS 引起的肠道损伤的潜在保护机制。通过将雄性 C57BL/6J 小鼠(5-6 周龄,17-19g)暴露于(34±0.7)℃下 4 周来建立动物 HA 模型,建立了 HA 模型。通过 16S rRNA 基因测序和非靶向液相色谱-质谱(LC-MS)代谢组学研究了 HA 对 HS 引起的肠道屏障损伤的保护作用。根据实验结果,HA 可以改变肠道微生物群的组成,增加乳杆菌、粪便细菌和尿细菌的比例,但降低脱氧胆酸的比例。此外,HA 可以减轻 HS 引起的肝肾功能损伤和全身炎症,通过增强肠道屏障的完整性来减轻肠道损伤。此外,HA 通过抑制 NF-κB 信号通路和增加 HS 小鼠中紧密连接蛋白的表达来调节炎症。HA 诱导肠道微生物群的变化,这可能增强紧密连接蛋白的表达,从而减少肠道炎症,促进胆汁酸代谢,最终维持肠道屏障的完整性。总之,HA 诱导了肠道微生物群的变化。在肠道微生物群中,乳杆菌可能在 HA 的潜在保护机制中发挥关键作用。