College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, China.
College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, China.
Eur J Pharmacol. 2021 Mar 15;895:173885. doi: 10.1016/j.ejphar.2021.173885. Epub 2021 Jan 19.
Huge of previous reports recommended that gut microbiome have a crucial role in the human health and its change was profound impact for the metabolic improvements associated with lipids metabolism. In order to explore the relevance of a direct dysbiosis effect of gut microbiome on lipids metabolism shifts and repaired position of DHA, we built the animal model for the study with gut microbiome dysbiosis administrated by i.g. with CRO and intervened by DHA in the present work. Gut microbiome was analyzed by high throughput sequencing and bioinformatics analyses of bacteria. The composition of fatty acids and short chain fatty acids (SCFAs) were determined by gas chromatography. Blood lipids and bile acids were assayed by kit and UPLC-MS/MS, respectively. The expressions of enzymes of long chain fatty acid metabolism were analyzed by qRT-PCR. The results showed that gut microbiome dysbiosis caused lipid metabolism abnormal, and DHA was able to repair the lipids metabolism shifts resulted from gut microbiome dysbiosis. DHA could modulate host-gut microbiome signatures, improve concentrations of SCFAs, regulate fatty acids metabolism but modify bile acid profiles. In conclusion, we considered that DHA repaired lipid metabolism by modulating gut microbiome and regulating fatty acids metabolism pathway.
大量先前的报告表明,肠道微生物组在人类健康中起着至关重要的作用,其变化对与脂质代谢相关的代谢改善有着深远的影响。为了探索肠道微生物组对脂质代谢变化的直接失调作用以及对 DHA 修复位置的相关性,我们在本工作中通过 i.g. 用 CRO 进行肠道微生物组失调处理,并通过 DHA 进行干预,建立了动物模型进行研究。通过高通量测序和细菌的生物信息学分析来分析肠道微生物组。通过气相色谱法测定脂肪酸和短链脂肪酸 (SCFA) 的组成。通过试剂盒和 UPLC-MS/MS 分别测定血脂和胆汁酸。通过 qRT-PCR 分析长链脂肪酸代谢酶的表达。结果表明,肠道微生物组失调导致脂质代谢异常,而 DHA 能够修复肠道微生物组失调引起的脂质代谢紊乱。DHA 可以调节宿主-肠道微生物组特征,增加 SCFA 的浓度,调节脂肪酸代谢,但改变胆汁酸谱。总之,我们认为 DHA 通过调节肠道微生物组和调节脂肪酸代谢途径来修复脂质代谢。