Department of Microbiology, Xiangya School of Medicine, Central South University, Changsha 410078, China.
Exp Biol Med (Maywood). 2020 Mar;245(6):512-521. doi: 10.1177/1535370219898407. Epub 2020 Jan 7.
Studies have shown that metabolic diseases, such as obesity, are significantly associated with intestinal flora imbalance. The amplification of opportunistic pathogens induced by the glyoxylic acid cycle contributes to intestinal flora imbalance. Promising, though, is that saturated hydrogen can effectively improve the occurrence and development of metabolic diseases, such as obesity. However, the specific mechanism of how saturated hydrogen operates is still not very clear. In this study, after a high-fat diet, the level of total cholesterol, total glyceride, and low-density lipoprotein in the peripheral blood of mice increased, and that of high-density lipoprotein decreased. Intestinal fatty acid metabolism-related gene Apolipoprotein E (ApoE), fatty acid synthase (FAS), intestinal fatty acid-binding protein (I-FAPB), acetyl-CoA carboxylase 1 (ACC1), peroxisome proliferator-activated receptor γ (PPARγ), and stearoyl-CoA desaturase 1 (SCD1) increased significantly. , , and counts in feces decreased considerably, while increased. The activity of isocitrate lyase in feces increased markedly. Treatment of mice with saturated hydrogen led to decreased total cholesterol, total glyceride, and low-density lipoprotein and increased high-density lipoprotein in the peripheral blood. FAS and I-FAPB gene expression in the small intestine decreased. , and in feces increased significantly, whereas decreased. The activity of isocitrate lyase also diminished remarkably. These results suggest that saturated hydrogen could improve intestinal structural integrity and lipid metabolism disorders by inhibiting the glyoxylic acid cycle of the intestinal flora.
Past studies have shown that hydrogen can improve metabolic disorders, but its mechanism of action remains unclear. It is well known that metabolic diseases, such as obesity, are significantly associated with changes in the intestinal flora. The glyoxylic acid cycle is an essential metabolic pathway in prokaryotes, lower eukaryotes, and plants and could be the portal for mechanisms related to metabolic disorders. Many opportunistic pathogenic bacteria can recycle fatty acids to synthesize sugars and other pathogenic substances using the glyoxylic acid cycle. So, the glyoxylic acid cycle may be involved in intestinal dysbacteriosis under high-fat diet. This study, therefore, seeks to provide the mechanism of how hydrogen improves metabolic diseases and a new basis for the use of hydrogen in the treatment of metabolic disorders.
研究表明,代谢性疾病(如肥胖症)与肠道菌群失衡显著相关。乙醛酸循环诱导的机会性病原体的扩增导致肠道菌群失衡。值得注意的是,饱和氢气可以有效改善肥胖症等代谢性疾病的发生和发展。然而,饱和氢气如何运作的具体机制尚不清楚。在这项研究中,高脂饮食后,小鼠外周血总胆固醇、总甘油三酯和低密度脂蛋白水平升高,高密度脂蛋白水平降低。肠道脂肪酸代谢相关基因载脂蛋白 E(ApoE)、脂肪酸合酶(FAS)、肠脂肪酸结合蛋白(I-FAPB)、乙酰辅酶 A 羧化酶 1(ACC1)、过氧化物酶体增殖物激活受体 γ(PPARγ)和硬脂酰辅酶 A 去饱和酶 1(SCD1)显著增加。粪便中 、 和 的数量明显减少,而 增加。粪便中异柠檬酸裂解酶活性显著增加。用饱和氢气处理小鼠可使外周血总胆固醇、总甘油三酯和低密度脂蛋白降低,高密度脂蛋白升高。小肠 FAS 和 I-FAPB 基因表达降低。粪便中 、 和 显著增加,而 减少。异柠檬酸裂解酶活性也显著降低。这些结果表明,饱和氢气通过抑制肠道菌群的乙醛酸循环,改善肠道结构完整性和脂质代谢紊乱。
过去的研究表明,氢气可以改善代谢紊乱,但作用机制尚不清楚。众所周知,肥胖症等代谢性疾病与肠道菌群的变化显著相关。乙醛酸循环是原核生物、低等真核生物和植物中一种重要的代谢途径,可能是与代谢紊乱相关机制的门户。许多机会性病原体可以使用乙醛酸循环回收脂肪酸来合成糖和其他致病物质。因此,在高脂肪饮食下,乙醛酸循环可能与肠道菌群失调有关。因此,本研究旨在提供氢气改善代谢性疾病的机制,并为氢气在治疗代谢性疾病中的应用提供新的依据。