Xu Zhenxia, Tang Hu, Huang Fenghong, Qiao Zhixian, Wang Xu, Yang Chen, Deng Qianchun
Oil Crops and Lipids Process Technology National and Local Joint Engineering Laboratory, Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Wuhan, China.
Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.
Front Microbiol. 2020 Dec 16;11:615404. doi: 10.3389/fmicb.2020.615404. eCollection 2020.
Algal oil is rich in docosahexaenoic acid (DHA) and has various health benefits against human metabolic disorders and disease. This study aimed to investigate the effects of DHA algal oil on colonic inflammation and intestinal microbiota in dextran sulfate sodium (DSS)-induced colitis mice model. Male C57BL/6 mice was induced colitis by 2.5% DSS and followed by 2 weeks of treatment with algal oil (250 or 500 mg/kg/day). The colonic inflammation was assessed by colon macroscopic damage scores, and the degree of neutrophil infiltration was evaluated by measuring tissue-associated myeloperoxidase (MPO) activity in colonic mucosa. Tight junction proteins in the colonic tissue were measured by real-time PCR and western blot. Moreover, the intestinal microbiota and shot chain fatty acids (SCFAs) were estimated by bioinformatic analysis and GC, respectively. Colonic damage due to DSS treatment was significantly ameliorated by algal oil supplementation. In addition, algal oil significantly inhibited the increases of malondialdehyde (MDA) content, MPO activity, pro-inflammatory cytokines level and tight junction proteins expression in DSS-treated mice. Furthermore, supplementation of algal oil modulated the intestinal microbiota structure in DSS induced colitis mice by increasing the proportion of the and decreasing the relative abundance of , . On the analysis of SCFAs, the caecal content of acetic acid, propionic acid, isobutyric acid, buturic, and the total SCFAs showed a significant increase in algal oil-administered mice. Together, these results suggested that algal oil rich in DHA inhibited the progress of DSS-induced colitis in mice by modulating the intestinal microbiota and metabolites and repairing the intestinal barrier, which may be applied in the development of therapeutics for intestinal inflammation.
藻油富含二十二碳六烯酸(DHA),对人类代谢紊乱和疾病具有多种健康益处。本研究旨在探讨DHA藻油对葡聚糖硫酸钠(DSS)诱导的结肠炎小鼠模型结肠炎症和肠道微生物群的影响。雄性C57BL/6小鼠用2.5% DSS诱导结肠炎,随后用藻油(250或500毫克/千克/天)治疗2周。通过结肠宏观损伤评分评估结肠炎症,通过测量结肠黏膜中与组织相关的髓过氧化物酶(MPO)活性评估中性粒细胞浸润程度。通过实时PCR和蛋白质印迹法测量结肠组织中的紧密连接蛋白。此外,分别通过生物信息分析和气相色谱法估计肠道微生物群和短链脂肪酸(SCFA)。补充藻油可显著改善DSS治疗引起的结肠损伤。此外,藻油显著抑制DSS处理小鼠中丙二醛(MDA)含量、MPO活性、促炎细胞因子水平和紧密连接蛋白表达的增加。此外,补充藻油通过增加[具体菌属1]的比例和降低[具体菌属2]、[具体菌属3]的相对丰度来调节DSS诱导的结肠炎小鼠的肠道微生物群结构。在对SCFA的分析中,给予藻油的小鼠盲肠内容物中乙酸、丙酸、异丁酸、丁酸以及总SCFA均显著增加。总之,这些结果表明,富含DHA的藻油通过调节肠道微生物群和代谢产物以及修复肠道屏障来抑制小鼠DSS诱导的结肠炎进展,这可能应用于肠道炎症治疗药物的开发。