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虾青素通过调节小鼠肠道微生物群预防酒精性脂肪肝疾病。

Astaxanthin Prevents Alcoholic Fatty Liver Disease by Modulating Mouse Gut Microbiota.

机构信息

School of Life Sciences, Jilin University, Changchun 130012, China.

College of Food Science and Engineering, Jilin Agricultural University, Changchun 130118, China.

出版信息

Nutrients. 2018 Sep 13;10(9):1298. doi: 10.3390/nu10091298.

Abstract

The development and progression of alcoholic fatty liver disease (AFLD) is influenced by the intestinal microbiota. Astaxanthin, a type of oxygenated carotenoid with strong antioxidant and anti-inflammatory properties, has been proven to relieve liver injury. However, the relationship between the gut microbiota regulation effect of astaxanthin and AFLD improvement remains unclear. The effects of astaxanthin on the AFLD phenotype, overall structure, and composition of gut microbiota were assessed in ethanol-fed C57BL/6J mice. The results showed that astaxanthin treatment significantly relieves inflammation and decreases excessive lipid accumulation and serum markers of liver injury. Furthermore, astaxanthin was shown to significantly decrease species from the phyla Bacteroidetes and Proteobacteria and the genera , , and , as well as increase species from Verrucomicrobia and compared with the Et (ethanol)group. Thirteen phylotypes related to inflammation as well as correlated with metabolic parameters were significantly altered by ethanol, and then notably reversed by astaxanthin. Additionally, astaxanthin altered 18 and 128 KEGG (Kyoto Encyclopedia of Genes and Genomes) pathways involved in lipid metabolism and xenobiotic biodegradation and metabolism at levels 2 and 3, respectively. These findings suggest that may be a potential target for the astaxanthin-induced alleviation of AFLD and may be a potential treatment for bacterial disorders induced by AFLD.

摘要

酒精性脂肪肝疾病(AFLD)的发展和进展受到肠道微生物群的影响。虾青素是一种具有强大抗氧化和抗炎特性的含氧类胡萝卜素,已被证明可缓解肝损伤。然而,虾青素对肠道微生物群调节作用与 AFLD 改善之间的关系仍不清楚。本研究在乙醇喂养的 C57BL/6J 小鼠中评估了虾青素对 AFLD 表型、整体结构和肠道微生物群组成的影响。结果表明,虾青素治疗可显著缓解炎症,减少过量脂质积累和血清肝损伤标志物。此外,与 Et(乙醇)组相比,虾青素显著降低了厚壁菌门和变形菌门以及 、 、 和 属的物种丰度,并增加了疣微菌门和 属的物种丰度。与代谢参数相关的 13 个与炎症相关的生物型受乙醇显著改变,然后被虾青素显著逆转。此外,虾青素分别在第 2 级和第 3 级改变了与脂质代谢和外源生物降解和代谢相关的 18 个和 128 个 KEGG(京都基因与基因组百科全书)途径。这些发现表明 可能是虾青素缓解 AFLD 的潜在靶点,也可能是 AFLD 诱导的细菌紊乱的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/829f/6164583/a4129d795105/nutrients-10-01298-g001.jpg

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