分子氢刺激转录辅激活因子 PGC-1α 的基因表达,促进脂肪酸代谢

IF 4.1 Q2 GERIATRICS & GERONTOLOGY
npj aging Pub Date : 2016-04-28 DOI:10.1038/npjamd.2016.8
Naomi Kamimura, Harumi Ichimiya, Katsuya Iuchi, Shigeo Ohta
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引用次数: 50

摘要

我们曾报道过分子氢(H2)作为一种新型抗氧化剂具有多种功能。此外,长期饮用 H2 水(注入 H2 的水)可增强能量消耗,从而改善 db/db 小鼠的肥胖和糖尿病,同时还可增加成纤维细胞生长因子 21(FGF21)的表达,其机制尚不清楚。H2是通过饮用H2水或口服H2产生物质MgH2摄入的。通过 DNA 微阵列分析了 db/db 小鼠肝脏中全面的基因表达谱。利用培养的 HepG2 细胞研究了基因表达谱的分子机制。此外,还使用以脂肪为食物的野生型小鼠研究了饮用 H2 水对寿命的影响。基于综合基因表达的通路分析表明,涉及脂肪酸和类固醇代谢的各种基因的表达增加。作为一种转录途径,PPARα 信号通路被确定为摄入 H2 后上调这些基因的途径。作为早期事件,PGC-1α 基因表达短暂增加,随后 FGF21 的表达增加。正如培养细胞实验所表明的那样,PGC-1α的表达可能是通过H2、4-羟基-2-壬烯醛和Akt/FoxO1信号传导的连续调节间接调控的。在喂食脂肪饮食的野生型小鼠中,H2-水改善了血浆甘油三酯的水平,延长了它们的平均寿命。氢能诱导 PGC-1α 基因的表达,随后刺激 PPARα 通路,从而调节 FGF21 以及脂肪酸和类固醇代谢。口服分子氢(H2)可激活在脂肪酸代谢中起关键作用的基因。氢气可以防止氧化化合物对细胞造成的损害,之前的一项研究表明,注入氢气的水可以改善遗传性肥胖啮齿动物的代谢健康。为了确定潜在的作用机制,日本医科大学的研究人员在 Shigeo Ohta 的带领下,给肥胖小鼠注射了两周的 H2 水。在动物的健康状况没有发生明显变化之前,研究人员观察到肝脏中调节类固醇和脂肪酸代谢的通路中几个基因的表达发生了明显变化。这种治疗还与喂食高脂肪饮食的基因正常小鼠血液中甘油三酯的降低有关,表明这种治疗可以诱导临床上有用的新陈代谢反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular hydrogen stimulates the gene expression of transcriptional coactivator PGC-1α to enhance fatty acid metabolism

Molecular hydrogen stimulates the gene expression of transcriptional coactivator PGC-1α to enhance fatty acid metabolism
We previously reported that molecular hydrogen (H2) acts as a novel antioxidant to exhibit multiple functions. Moreover, long-term drinking of H2-water (water infused with H2) enhanced energy expenditure to improve obesity and diabetes in db/db mice accompanied by the increased expression of fibroblast growth factor 21 (FGF21) by an unknown mechanism. H2 was ingested by drinking of H2-water or by oral administration of an H2-producing material, MgH2. The comprehensive gene expression profile in the liver of db/db mice was analyzed by DNA microarray. The molecular mechanisms underlying the gene expression profile was investigated using cultured HepG2 cells. Moreover, the effects on lifespan of drinking H2-water were examined using wild-type mice that were fed a fatty diet. Pathway analyses based on comprehensive gene expression revealed the increased expression of various genes involved in fatty acid and steroid metabolism. As a transcription pathway, the PPARα signaling pathway was identified to upregulate their genes by ingesting H2. As an early event, the gene expression of PGC-1α was transiently increased, followed by increased expression of FGF21. The expression of PGC-1α might be regulated indirectly through sequential regulation by H2, 4-hydroxy-2-nonenal, and Akt/FoxO1 signaling, as suggested in cultured cell experiments. In wild-type mice fed the fatty diet, H2-water improved the level of plasma triglycerides and extended their average of lifespan. H2 induces expression of the PGC-1α gene, followed by stimulation of the PPARα pathway that regulates FGF21, and the fatty acid and steroid metabolism. Oral consumption of molecular hydrogen (H2) activates genes with a critical role in fatty acid metabolism. H2 can prevent the cellular damage caused by oxidizing chemical compounds, and a previous study suggested that water infused with H2 can improve metabolic health in genetically obese rodents. In order to identify a potential mechanism of action, researchers led by Shigeo Ohta at Nippon Medical School dosed obese mice with H2-infused water for two weeks. Before the animals'' health did not notably change, the researchers observed clear changes in the expression of several genes in a pathway that regulate the metabolism of steroids and fatty acids in the liver. This treatment was also associated with lower blood triglycerides in genetically normal mice fed a high-fat diet, suggesting that such treatments could induce a clinically useful metabolic response.
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