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首页> 外文期刊>Journal of Lipid Research >Administration of a PPARalpha agonist increases serum apolipoprotein A-V levels and the apolipoprotein A-V/apolipoprotein C-III ratio.
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Administration of a PPARalpha agonist increases serum apolipoprotein A-V levels and the apolipoprotein A-V/apolipoprotein C-III ratio.

机译:PPARalpha激动剂的使用会增加血清载脂蛋白A-V水平和载脂蛋白A-V /载脂蛋白C-III的比例。

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摘要

Apolipoprotein A-V (apoA-V) first gained attention as a regulator of triglycerides through transgenic mouse studies. Furthermore, peroxisome proliferator-activated receptor alpha (PPARalpha) agonists such as fenofibrate increase apoA-V mRNA expression. Our group recently developed the first assay to quantitate serum apoA-V levels. Therefore, we sought to determine whether administration of a PPARalpha agonist would increase circulating apoA-V. Cynomolgus monkeys were dosed for 14 days with 0.3 mg/kg/day LY570977 L-lysine, a potent and selective PPARalpha agonist. Blood samples were drawn throughout the treatment period and after a 2 week washout. Administration of the PPARalpha agonist caused a 50% decrease in triglycerides that reversed at washout. Serum apoA-V concentrations increased 2-fold, correlated inversely with triglycerides, and were reversible at washout. The apoA-V/apoC-III ratio increased >2-fold, with this increase also reversible at washout. These data demonstrate for the first time thata PPARalpha agonist increases circulating apoA-V protein levels and the apoA-V/apoC-III ratio.
机译:通过转基因小鼠研究,载脂蛋白A-V(apoA-V)作为甘油三酸酯的调节剂首次受到关注。此外,过氧化物酶体增殖物激活的受体α(PPARalpha)激动剂(如非诺贝特)可增加apoA-V mRNA的表达。我们小组最近开发了第一种定量血清apoA-V水平的检测方法。因此,我们试图确定施用PPARα激动剂是否会增加循环apoA-V。食蟹猴用0.3 mg / kg /天的LY570977 L-赖氨酸(一种有效的选择性PPARα激动剂)给药14天。在整个治疗期间和2周冲洗后抽取血样。 PPARalpha激动剂的使用导致甘油三酯降低50%,甘油三酸酯在冲洗时会逆转。血清apoA-V浓度增加2倍,与甘油三酸酯成反比,在洗脱时可逆。 apoA-V / apoC-III比率增加> 2倍,并且这种增加在洗脱时也是可逆的。这些数据首次证明,PPARalpha激动剂可增加循环的apoA-V蛋白水平和apoA-V / apoC-III比率。

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