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首页> 外文期刊>The FEBS journal >Transcriptome profiling analysis reveals multiple modulatory effects of Ginkgo biloba extract in the liver of rats on a high-fat diet
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Transcriptome profiling analysis reveals multiple modulatory effects of Ginkgo biloba extract in the liver of rats on a high-fat diet

机译:转录组图谱分析揭示了高脂饮食对大鼠肝脏中银杏叶提取物的多种调节作用

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摘要

Leaf extract of Ginkgo biloba (GBE) is increasingly used as a herbal medicine for the treatment of neurodegenerative, cardiovascular and cerebrovascular diseases. Several studies have demonstrated many protective effects of GBE in neurons, the endothelium and liver. In this study, we investigated the molecular mechanisms underlying the effects of GBE in disorders induced by long-term exposure to a high-fat diet (HFD). Rats were fed an HFD with or without the GBE product GBE50 for 19 weeks. We found that GBE50 reduced the development of fatty liver induced by an HFD and inhibited the commonly observed elevation of serum cholesterol and lactate dehydrogenase levels. Transcriptome profiling analysis showed that several genes were modulated by GBE50 in liver, including those involved in lipid metabolism, carbohydrate metabolism, vascular constriction, ion transportation, neuronal systems and drug metabolism. Notably, a number of genes coding for proteins involved in cholesterol metabolism were repressed, and some were upregulated. Fatty acid biosynthesis appeared to be repressed, whereas fatty acid metabolism appeared to be enhanced. In conclusion, using transcriptome profiling analysis, we demonstrated the molecular basis for the pleiotropic effects of GBE50, particularly those involved in lipid metabolism. This study provided new clues for further pharmacological study of GBEs.
机译:银杏叶提取物(GBE)越来越多地用作治疗神经退行性,心血管和脑血管疾病的草药。多项研究表明,GBE对神经元,内皮和肝脏具有许多保护作用。在这项研究中,我们调查了GBE在长期暴露于高脂饮食(HFD)引起的疾病中的潜在分子机制。给大鼠喂食含或不含GBE产品GBE50的HFD,持续19周。我们发现GBE50减少了由HFD诱导的脂肪肝的发展,并抑制了通常观察到的血清胆固醇和乳酸脱氢酶水平的升高。转录组谱分析表明,GBE50在肝脏中调节了多个基因,包括与脂质代谢,碳水化合物代谢,血管收缩,离子转运,神经元系统和药物代谢有关的基因。值得注意的是,许多编码参与胆固醇代谢的蛋白质的基因被抑制,有些则被上调。脂肪酸的生物合成似乎受到抑制,而脂肪酸的代谢似乎得到增强。总之,使用转录组谱分析,我们证明了GBE50的多效性作用的分子基础,尤其是涉及脂质代谢的作用。该研究为GBE的进一步药理研究提供了新的线索。

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