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

机译:暴露于慢性低管缺氧的大鼠中的血浆和肝脂肪曲线:代谢途径的变化

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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:在慢性缺氧(CH)下的脂质代谢尚未接受平等的关注,因为间歇性缺氧(IH)。确定血浆和肝脏中的CH诱导的变化,以及甘油三酯和胆固醇生物合成途径,SrebP-1(HMG-CoA还原酶)和Srebp-2(SCD-1)中的两个关键酶的mRNA和蛋白表达。与常氧大鼠相比,我们将成年雄性Wistar大鼠暴露于CH(4600m; n = 15)30天(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,总胆固醇和LDL-胆固醇在第15天增加。VLDL-胆固醇和甘油三酯(P <0.01)大大增加(35%),而HDL-胆固醇降低(P <0.01)。在第30天,甘油三酯和VLDL-胆固醇保持升高28%(P <0.01)。肝甘油三酯增加了两倍,而总胆固醇增加51%(P <0.001; P <0.05)。在CH大鼠中观察到SCD-1 mRNA和蛋白质的上调(P <0.01);然而,在两组中,在HMG-CoA还原酶mRNA或蛋白质表达中没有观察到差异。总之,CH,如Ih,通过增加血浆和肝脏中的甘油三酯和上调甘油三酯生物合成而改变脂质曲线,而不影响胆固醇生物合成途径。由于脂质在心血管风险的重要性,额外的涉及机制需要进一步研究。

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