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Plasma and Liver Lipid Profiles in Rats Exposed to Chronic Hypobaric Hypoxia: Changes in Metabolic Pathways

机译:暴露于慢性低压缺氧的大鼠的血浆和肝脂质谱:代谢途径的变化

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摘要

Siques, Patricia, Julio Brito, Nelson Naveas, Ruth Pulido, Juan José De la Cruz, Maribel Mamani, and Fabiola León-Velarde. Plasma and liver lipid profiles in rats exposed to chronic hypobaric hypoxia: Changes in metabolic pathways. High Alt Med Biol 15:388–395, 2014.—Lipid metabolism under chronic hypoxia (CH) has not received equal attention as intermittent hypoxia (IH). To determine the CH-induced changes in plasma and liver, as well as the mRNA and protein expression of two key enzymes in the triglyceride and cholesterol biosynthesis pathways, SREBP-1 (HMG-CoA reductase) and SREBP-2 (SCD-1), we exposed adult male Wistar rats to CH (4600 m; n=15) for 30 days compared to normoxic rats (n=15). The CH rats exhibited weight loss (p<0.001), higher hematocrit (%), and higher hemoglobin (g/dL) (p<0.01). In the plasma of CH rats, total cholesterol and LDL-cholesterol increased at day 15. VLDL-cholesterol and triglycerides (p<0.01) greatly increased (35%), while HDL-cholesterol decreased (p<0.01). Triglycerides and VLDL-cholesterol remained elevated by 28% at day 30 (p<0.01). Hepatic triglycerides increased two-fold, while total cholesterol increased by 51% (p<0.001; p<0.05). Upregulation of SCD-1 mRNA and protein was observed in the CH rats (p<0.01); however, no differences were observed in HMG-CoA reductase mRNA or protein expression in both groups. In conclusion, CH, like IH, alters lipid profiles by increasing triglycerides in the plasma and liver and upregulating triglyceride biosynthesis without affecting the cholesterol biosynthetic pathway. Additional involved mechanisms require further study because of the importance of lipids in cardiovascular risk.
机译:Siques,Patricia,Julio Brito,Nelson Naveas,Ruth Pulido,JuanJoséDe la Cruz,Maribel Mamani和FabiolaLeón-Velarde。暴露于慢性低压缺氧大鼠的血浆和肝脂质谱:代谢途径的变化。 High Alt Med Biol 15:388-395,2014年。慢性缺氧(CH)下的脂类代谢没有像间歇性缺氧(IH)受到同样的重视。要确定CH诱导的血浆和肝脏变化,以及甘油三酸酯和胆固醇生物合成途径中的两个关键酶的mRNA和蛋白表达,即SREBP-1(HMG-CoA还原酶)和SREBP-2(SCD-1) ,我们将成年雄性Wistar大鼠暴露于CH(4600 m; n = 15)30天,而正常氧大鼠(n = 15)。 CH大鼠表现出体重减轻(p <0.001),更高的血细胞比容(%)和更高的血红蛋白(g / dL)(p <0.01)。在CH大鼠的血浆中,第15天的总胆固醇和LDL-胆固醇升高(VLDL-胆固醇和甘油三酸酯(p <0.01))大大增加(35%),而HDL-胆固醇降低(p <0.01)。在第30天,甘油三酸酯和VLDL-胆固醇保持升高28%(p <0.01)。肝甘油三酸酯增加了两倍,而总胆固醇增加了51%(p <0.001; p <0.05)。在CH大鼠中观察到SCD-1 mRNA和蛋白的上调(p <0.01);然而,两组均未观察到HMG-CoA还原酶mRNA或蛋白表达的差异。总之,CH与IH一样,通过增加血浆和肝脏中的甘油三酸酯和上调甘油三酸酯的生物合成来改变脂质谱,而不会影响胆固醇的生物合成途径。由于脂质在心血管风险中的重要性,因此其他相关机制尚需进一步研究。

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