丁酸盐对热应激诱导的肠道损伤、全身炎症和多器官功能障碍的治疗潜力:来自体外和体内实验的见解

IF 4.2 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Hung-Yen Ke , Ming-Hua Chen , Cheng-Ming Tsao , Hiong-Ping Hii , Chia-Wen Kuo , Shuk-Man Ka , Chin-Chen Wu , Chih-Chin Shih
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引用次数: 0

摘要

全球变暖是危及生命的中暑(HS)的主要危险因素。全身性炎症在HS的病理生理中起着关键作用,严重影响临床结果。HS时肠道血流量减少导致缺血再灌注损伤,破坏肠道屏障,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、减轻氧化应激等方面发挥着多方面的作用。因此,本研究旨在评价丁酸盐对HS的治疗潜力,并探讨其保护作用的机制。雄性Wistar大鼠分为4组:对照组、对照组+丁酸盐组、HS组和HS +丁酸盐组。分析血液动力学变化、生化指标、凝血指标、细胞因子水平、多形核中性粒细胞浸润及生存率。此外,利用大鼠回肠样本和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;降低肠杯状细胞的上皮耐药;引发HS大鼠肠道炎症、氧化应激和细胞凋亡。这些大鼠表现出全身性炎症、低血压、心动过速、凝血功能障碍、多器官功能障碍和死亡。丁酸盐处理降低了LS174T细胞的细胞毒性并改善了经皮细胞耐药性。丁酸盐还能降低HS大鼠肠道热应激、炎症、氧化应激、细胞凋亡及全身炎症。此外,丁酸改善了HS大鼠的低血压、心动过速、凝血功能障碍和多器官功能障碍,并提高了生存率。这些发现表明,丁酸盐是一种很有希望的干预措施,可以减轻热应激引起的肠道损伤、全身炎症和多器官功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Therapeutic potential of butyrate against heat Stress–Induced intestinal damage, systemic inflammation, and multiple organ Dysfunction: Insights from in vitro and in vivo experiments

Therapeutic potential of butyrate against heat Stress–Induced intestinal damage, systemic inflammation, and multiple organ Dysfunction: Insights from in vitro and in vivo experiments
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.
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来源期刊
CiteScore
9.00
自引率
0.00%
发文量
572
审稿时长
34 days
期刊介绍: The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems. The scope includes: Behavioural pharmacology Neuropharmacology and analgesia Cardiovascular pharmacology Pulmonary, gastrointestinal and urogenital pharmacology Endocrine pharmacology Immunopharmacology and inflammation Molecular and cellular pharmacology Regenerative pharmacology Biologicals and biotherapeutics Translational pharmacology Nutriceutical pharmacology.
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