Ke Hung-Yen, Chen Ming-Hua, Tsao Cheng-Ming, Hii Hiong-Ping, Kuo Chia-Wen, Ka Shuk-Man, Wu Chin-Chen, Shih Chih-Chin
Division of Cardiovascular Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Department of Internal Medicine, Taoyuan Armed Forces General Hospital, Taoyuan, Taiwan.
Eur J Pharmacol. 2025 Jul 15;999:177710. doi: 10.1016/j.ejphar.2025.177710. Epub 2025 May 8.
Global warming is a major risk factor for life-threatening heat stroke (HS). Systemic inflammation plays a key role in the pathophysiology of HS, substantially affecting clinical outcomes. Reduced intestinal blood flow during HS causes ischemia-reperfusion injury, compromising the intestinal barrier and triggering systemic inflammation and organ damage. Butyrate, a short-chain fatty acid, plays a multifaceted role in maintaining intestinal health, inhibiting inflammation, and alleviating oxidative stress. Therefore, this study aimed to evaluate butyrate's therapeutic potential against HS and explored the mechanisms underlying its protective effects. Male Wistar rats were divided into 4 groups: control, control + butyrate, HS, and HS + butyrate. Hemodynamic changes, biochemical parameters, coagulation markers, cytokine levels, polymorphonuclear neutrophil infiltration, and survival rates were analyzed. Additionally, ileal samples (from rats) and LS174T cells were used to investigate the effect of butyrate on intestinal function. Heat stress induced cytotoxicity; reduced transepithelial resistance in intestinal goblet cells; and triggered intestinal inflammation, oxidative stress, and apoptosis in HS rats. These rats exhibited systemic inflammation, hypotension, tachycardia, coagulopathy, multiple organ dysfunction, and mortality. Butyrate treatment reduced cytotoxicity and improved transepithelial resistance in LS174T cells. Butyrate also reduced intestinal heat stress, inflammation, oxidative stress, and apoptosis, as well as systemic inflammation in HS rats. Furthermore, butyrate ameliorated hypotension, tachycardia, coagulopathy, and multiple organ dysfunction and increased survival in HS rats. These findings indicate that butyrate is a promising intervention for mitigating heat stress-induced intestinal damage, systemic inflammation, and multiple organ dysfunction.
全球变暖是危及生命的中暑(HS)的主要风险因素。全身炎症在中暑的病理生理学中起关键作用,对临床结果有重大影响。中暑期间肠道血流减少会导致缺血再灌注损伤,损害肠道屏障并引发全身炎症和器官损伤。丁酸盐是一种短链脂肪酸,在维持肠道健康、抑制炎症和减轻氧化应激方面发挥多方面作用。因此,本研究旨在评估丁酸盐对中暑的治疗潜力,并探索其保护作用的潜在机制。雄性Wistar大鼠分为4组:对照组、对照组 + 丁酸盐组、中暑组和中暑 + 丁酸盐组。分析血流动力学变化、生化参数、凝血标志物、细胞因子水平、多形核中性粒细胞浸润和存活率。此外,使用(大鼠的)回肠样本和LS174T细胞研究丁酸盐对肠道功能的影响。热应激诱导细胞毒性;降低肠道杯状细胞的跨上皮电阻;并引发中暑大鼠的肠道炎症、氧化应激和细胞凋亡。这些大鼠表现出全身炎症、低血压、心动过速、凝血障碍、多器官功能障碍和死亡。丁酸盐治疗降低了LS174T细胞的细胞毒性并改善了跨上皮电阻。丁酸盐还减轻了中暑大鼠的肠道热应激、炎症、氧化应激和细胞凋亡,以及全身炎症。此外,丁酸盐改善了中暑大鼠的低血压、心动过速、凝血障碍和多器官功能障碍,并提高了存活率。这些发现表明,丁酸盐是减轻热应激诱导的肠道损伤、全身炎症和多器官功能障碍的一种有前景的干预措施。