首页> 美国卫生研究院文献>Marine Drugs >Magma Seawater Inhibits Hepatic Lipid Accumulation through Suppression of Lipogenic Enzymes Regulated by SREBPs in Thioacetamide-Injected Rats
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Magma Seawater Inhibits Hepatic Lipid Accumulation through Suppression of Lipogenic Enzymes Regulated by SREBPs in Thioacetamide-Injected Rats

机译:岩浆海水通过抑制SREBPs调节硫代乙酰胺注射大鼠的生脂酶来抑制肝脂质的积累。

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摘要

Thioacetamide (TAA) is known to induce lipid accumulation in the liver. In the present study, we investigated the effects of magma seawater (MS) rich in minerals on hepatic lipid metabolism by evaluating lipogenic enzymes regulated by sterol regulatory element-binding proteins (SREBPs). Rats (n = 10 per group) were intraperitoneally injected with TAA (200 mg/kg bw) thrice a week for seven weeks in combination with a respective experimental diet. Rats in the TAA-treated group received either a chow diet (Control group) or a chow diet containing MS (TMS group, 2.05%) or silymarin (TSM group, 0.05%). Rats in the normal group were injected with PBS as a vehicle and received a chow diet. Rats in the TMS group showed significantly lower hepatic lipid concentrations than rats in the control group (p < 0.05). Hepatic protein expression levels of fatty acid synthase, SREBP-1, 3-hydroxy-3-methylglutaryl-coenzyme A reductase, and SREBP-2 were significantly downregulated in the TMS group, whereas carnitine palmitoyltransferase 1 levels were upregulated (p < 0.05). Hepatic thiobarbituric acid reactive substances levels were lower in the TMS group, whereas protein levels of glutathione peroxidase and catalase were elevated (p < 0.05). The effects of MS were comparable to those of silymarin. Our results evidently showed that MS inhibits hepatic lipid accumulation by suppressing lipid synthesis, accompanied by lipid oxidation and elevation of antioxidative status.
机译:已知硫代乙酰胺(TAA)会引起肝脏中脂质的积累。在本研究中,我们通过评估由固醇调节元件结合蛋白(SREBPs)调节的生脂酶,研究了富含矿物质的岩浆海水(MS)对肝脂质代谢的影响。大鼠(每组n = 10)每周三次腹膜内注射TAA(200 mg / kg体重),并与相应的实验饮食相结合,共7周。 TAA治疗组的大鼠接受食物(对照组)或含MS的食物(TMS组,2.05%)或水飞蓟素(TSM组,0.05%)。正常组的大鼠注射PBS作为载体,并接受日常饮食。 TMS组的大鼠肝脂质浓度明显低于对照组(p <0.05)。在TMS组中,脂肪酸合酶,SREBP-1、3-羟基-3-甲基戊二酰辅酶A还原酶和SREBP-2的肝蛋白表达水平显着下调,而肉碱棕榈酰转移酶1的水平上调(p <0.05)。 TMS组的肝硫代巴比妥酸反应性物质水平较低,而谷胱甘肽过氧化物酶和过氧化氢酶的蛋白质水平升高(p <0.05)。 MS的效果与水飞蓟素相当。我们的结果显然表明,MS通过抑制脂质合成来抑制肝脏脂质的积累,并伴有脂质氧化和抗氧化状态的升高。

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