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基于肠道菌群调节的多糖对高脂血症大鼠的降血脂作用研究

Study on the hypolipidemic effect of polysaccharide in hyperlipidemia rats based on the regulation of intestinal flora.

作者信息

Lin Fengyuan, Li Xiao, Guo Xiao, Lu Xuechun, Han Xiao, Xu GuangYu, Du Peige, An Liping

机构信息

College of Pharmacy Beihua University Jilin China.

General Hospital of the People's Liberation Army Beijing China.

出版信息

Food Sci Nutr. 2022 Sep 25;11(1):191-203. doi: 10.1002/fsn3.3052. eCollection 2023 Jan.

Abstract

The purpose of this study was to observe the effect of polysaccharide (IOP) on blood lipids and its regulation on the intestinal flora in hyperlipidemia rats, and explore the modern biological connotation of IOP in reducing blood lipids. In this study, we obtained the crude IOP by the water extraction and alcohol precipitation method, and then classified it by DEAE ion-exchange chromatography to obtain the acidic polysaccharide (IOP-A). After the administration of the IOP-A, the serum TC, TG, and LDL-C levels were significantly lower, while the serum HDL-C levels were significantly higher. The expression of CYP7A1 protein was considerably increased, whereas the expression of SREBP-1C protein was considerably decreased in the rat hepatic tissue. In addition, the IOP-A could significantly alleviate the hepatocyte fatty degeneration in the liver lobule of rats. We believe that the IOP-A can affect the composition of intestinal flora by reducing the relative abundance of Firmicutes and increasing the relative abundance of Bacteroidetes. These findings indicated that the IOP-A can regulate the dyslipidemia of hyperlipidemia rats, and its mechanism may be through regulating the CYP7A1 and SREBP-1C expression in the metabolism of lipids, and correcting the imbalance of intestinal flora structure caused by a high-fat diet.

摘要

本研究旨在观察多糖(IOP)对高脂血症大鼠血脂的影响及其对肠道菌群的调节作用,探讨IOP降血脂的现代生物学内涵。本研究采用水提醇沉法获得IOP粗品,再经DEAE离子交换色谱法进行分离得到酸性多糖(IOP-A)。给予IOP-A后,大鼠血清总胆固醇(TC)、甘油三酯(TG)和低密度脂蛋白胆固醇(LDL-C)水平显著降低,而血清高密度脂蛋白胆固醇(HDL-C)水平显著升高。大鼠肝组织中细胞色素P450 7A1(CYP7A1)蛋白表达明显增加,而固醇调节元件结合蛋白-1C(SREBP-1C)蛋白表达明显降低。此外,IOP-A可显著减轻大鼠肝小叶肝细胞脂肪变性。我们认为,IOP-A可通过降低厚壁菌门的相对丰度、增加拟杆菌门的相对丰度来影响肠道菌群的组成。这些结果表明,IOP-A可调节高脂血症大鼠血脂异常,其机制可能是通过调节脂质代谢中CYP7A1和SREBP-1C的表达,纠正高脂饮食引起的肠道菌群结构失衡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1b3/9834817/0c479c5aacd4/FSN3-11-191-g005.jpg

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