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Synthesis of a new [6]-gingerol analogue and its protective effect with respect to the development of metabolic syndrome in mice fed a high-fat diet

机译:高脂饮食小鼠新[6]-姜油类似物的合成及其对代谢综合征发展的保护作用

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摘要

To determine the effects of a [6]-gingerol analogue (6G), a major chemical component of the ginger rhizome, and its stable analogue after digestion in simulated gastric fluid, aza-[6]-gingerol (A6G), on diet-induced body fat accumulation, we synthesized 6G and A6G. Mice were fed either a control regular rodent chow, a high-fat diet (HFD), or a HFD supplemented with 6G and A6G. Magnetic resonance imaging adiposity parameters of the 6G- and A6G-treated mice were compared with those of control mice. Supplementation with 6G and A6G significantly reduced body weight gain, fat accumulation, and circulating levels of insulin and leptin. The mRNA levels of sterol regulatory element-binding protein 1c (SREBP-1c) and acetyl-CoA carboxylase 1 in the liver were significantly lower in mice fed A6G than in HFD control mice. Our findings indicate that A6G, rather than 6G, enhances energy metabolism and reduces the extent of lipogenesis by downregulating SREBP-1c and its related molecules, which leads to the suppression of body fat accumulation.
机译:为了确定姜根茎的主要化学成分[6]-姜粉类似物(6G)及其在模拟胃液aza- [6]-姜粉(A6G)中消化后的稳定类似物对饮食的影响,诱导体内脂肪积累,我们合成了6G和A6G。给小鼠喂食常规的啮齿动物饲料,高脂饮食(HFD)或补充了6G和A6G的HFD。将6G和A6G治疗小鼠的磁共振成像肥胖参数与对照小鼠进行了比较。补充6G和A6G可以显着降低体重增加,脂肪堆积以及胰岛素和瘦素的循环水平。喂食A6G的小鼠肝脏中的固醇调节元件结合蛋白1c(SREBP-1c)和乙酰辅酶A羧化酶1的mRNA水平显着低于HFD对照小鼠。我们的发现表明,A6G而非6G通过下调SREBP-1c及其相关分子来增强能量代谢并减少脂肪生成的程度,从而抑制体内脂肪的积累。

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