Suppr超能文献

二十碳五烯酸增强 Caco-2 细胞热应激损伤的肠道上皮屏障功能。

Eicosapentaenoic acid enhances heat stress-impaired intestinal epithelial barrier function in Caco-2 cells.

机构信息

Guangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

PLoS One. 2013 Sep 16;8(9):e73571. doi: 10.1371/journal.pone.0073571. eCollection 2013.

Abstract

OBJECTIVE

Dysfunction of the intestinal epithelial tight junction (TJ) barrier is known to have an important etiologic role in the pathophysiology of heat stroke. N-3 polyunsaturated fatty acids (PUFAs), including eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), play a role in maintaining and protecting the TJ structure and function. This study is aimed at investigating whether n-3 PUFAs could alleviate heat stress-induced dysfunction of intestinal tight junction.

METHODS

Human intestinal epithelial Caco-2 cells were pre-incubated with EPA, DHA or arachidonic acid (AA) and then exposed to heat stress. Transepithelial electrical resistance (TEER) and Horseradish Peroxidase (HRP) permeability were measured to analyze barrier integrity. Levels of TJ proteins, including occludin, ZO-1 and claudin-2, were analyzed by Western blot and localized by immunofluorescence microscopy. Messenger RNA levels were determined by quantitative real time polymerase chain reaction (Q-PCR). TJ morphology was observed by transmission electron microscopy.

RESULTS

EPA effectively attenuated the decrease in TEER and impairment of intestinal permeability in HRP flux induced by heat exposure. EPA significantly elevated the expression of occludin and ZO-1, while DHA was less effective and AA was not at all effective. The distortion and redistribution of TJ proteins, and disruption of morphology were also effectively prevented by pretreatment with EPA.

CONCLUSION

This study indicates for the first time that EPA is more potent than DHA in protecting against heat-induced permeability dysfunction and epithelial barrier damage of tight junction.

摘要

目的

已知肠道上皮紧密连接 (TJ) 屏障功能障碍在中暑的病理生理学中具有重要的病因作用。n-3 多不饱和脂肪酸 (PUFA),包括二十碳五烯酸 (EPA) 和二十二碳六烯酸 (DHA),在维持和保护 TJ 结构和功能方面发挥作用。本研究旨在探讨 n-3 PUFAs 是否可以减轻热应激引起的肠道紧密连接功能障碍。

方法

人肠道上皮 Caco-2 细胞用 EPA、DHA 或花生四烯酸 (AA) 预孵育,然后暴露于热应激下。通过测定跨上皮电阻 (TEER) 和辣根过氧化物酶 (HRP) 通透性来分析屏障完整性。通过 Western blot 分析 TJ 蛋白(包括闭合蛋白、ZO-1 和 Claudin-2)的水平,并通过免疫荧光显微镜定位。通过定量实时聚合酶链反应 (Q-PCR) 测定信使 RNA 水平。通过透射电子显微镜观察 TJ 形态。

结果

EPA 有效减弱了热暴露引起的 TEER 下降和 HRP 通量引起的肠道通透性损伤。EPA 显著上调了闭合蛋白和 ZO-1 的表达,而 DHA 效果较差,AA 则完全无效。TJ 蛋白的扭曲和重分布以及形态的破坏也被 EPA 的预处理有效阻止。

结论

本研究首次表明,EPA 在保护热诱导的通透性功能障碍和紧密连接上皮屏障损伤方面比 DHA 更有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a31f/3774713/2a8716b4ad05/pone.0073571.g001.jpg

相似文献

1
Eicosapentaenoic acid enhances heat stress-impaired intestinal epithelial barrier function in Caco-2 cells.
PLoS One. 2013 Sep 16;8(9):e73571. doi: 10.1371/journal.pone.0073571. eCollection 2013.
3
Akkermansia muciniphila improves heat stress-impaired intestinal barrier function by modulating HSP27 in Caco-2 cells.
Microb Pathog. 2023 Apr;177:106028. doi: 10.1016/j.micpath.2023.106028. Epub 2023 Feb 14.
6
Mycophenolic acid mediated disruption of the intestinal epithelial tight junctions.
Exp Cell Res. 2014 Apr 1;322(2):277-89. doi: 10.1016/j.yexcr.2014.01.021. Epub 2014 Feb 7.
9
Physiologically relevant increase in temperature causes an increase in intestinal epithelial tight junction permeability.
Am J Physiol Gastrointest Liver Physiol. 2006 Feb;290(2):G204-12. doi: 10.1152/ajpgi.00401.2005.

引用本文的文献

1
Molecular Mechanisms Linking Omega-3 Fatty Acids and the Gut-Brain Axis.
Molecules. 2024 Dec 28;30(1):71. doi: 10.3390/molecules30010071.
4
Potential of nutraceuticals in celiac disease.
Tissue Barriers. 2025;13(2):2374628. doi: 10.1080/21688370.2024.2374628. Epub 2024 Jun 30.
6
Effects of functional nutrients on chicken intestinal epithelial cells induced with oxidative stress.
J Anim Sci Technol. 2023 Sep;65(5):1040-1052. doi: 10.5187/jast.2023.e22. Epub 2023 Sep 30.
10
Drug-Induced Hyperthermia Review.
Cureus. 2022 Jul 26;14(7):e27278. doi: 10.7759/cureus.27278. eCollection 2022 Jul.

本文引用的文献

1
Omega-3 polyunsaturated fatty acids and inflammatory processes: nutrition or pharmacology?
Br J Clin Pharmacol. 2013 Mar;75(3):645-62. doi: 10.1111/j.1365-2125.2012.04374.x.
2
Modulation of tight junction structure and function by kinases and phosphatases targeting occludin.
J Biomed Biotechnol. 2012;2012:807356. doi: 10.1155/2012/807356. Epub 2012 Jan 23.
3
Methotrexate modulates tight junctions through NF-κB, MEK, and JNK pathways.
J Pediatr Gastroenterol Nutr. 2012 Apr;54(4):463-70. doi: 10.1097/MPG.0b013e318247240d.
5
Regulation of tight junction permeability by intestinal bacteria and dietary components.
J Nutr. 2011 May;141(5):769-76. doi: 10.3945/jn.110.135657. Epub 2011 Mar 23.
6
'Gut health': a new objective in medicine?
BMC Med. 2011 Mar 14;9:24. doi: 10.1186/1741-7015-9-24.
7
Role of eicosanoids on intestinal epithelial homeostasis.
Biochem Pharmacol. 2010 Aug 15;80(4):431-8. doi: 10.1016/j.bcp.2010.04.033. Epub 2010 May 10.
8
Inflammatory disease processes and interactions with nutrition.
Br J Nutr. 2009 May;101 Suppl 1:S1-45. doi: 10.1017/S0007114509377867.
10
Correlation of taurine transport with membrane lipid composition and peroxidation in DHA-enriched Caco-2 cells.
J Membr Biol. 2009 Apr;228(3):141-50. doi: 10.1007/s00232-009-9166-4. Epub 2009 Apr 7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验