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Up-regulation of PCSK9 gene expression and diminished level of LDL-receptor in rat liver as a potential cause of post-lipectomy hypercholesterolemia

机译:大鼠肝脏中PCSK9基因表达的上调和LDL受体水平的降低是脂肪切除术后高胆固醇血症的潜在原因

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摘要

Studies designed to examine effects of fat mass reduction (including lipodystrophy and lipectomy) on human serum total and LDL-cholesterol concentrations are inconsistent. The purpose of this study was to examine effect of partial lipectomy in rats (as an experimental model of fat mass reduction in humans) on (1) circulating total cholesterol, LDL-cholesterol + VLDL-cholesterol and HDL-cholesterol concentrations, and (2) factors which may affect serum cholesterol concentrations such as: (a) liver LDL-receptor level, (b) expression of liver PCSK9 and (c) circulating PCSK9 concentration. Reduction of rat adipose tissue mass resulted in an increase in circulating total and LDL + VLDL—cholesterol concentrations, which was associated with (a) decrease in liver LDL-R level, (b) increase in liver PCSK9 expression, and (c) increase in circulating PCSK9 concentration as compared with sham controls. These changes were accompanied by elevated liver HNF1α (and HNF4α) mRNA levels. Silencing HNF1α in HepG2 cells by siRNA led to decrease in PCSK9 mRNA levels. This suggests that overexpression of HNF1α gene in liver of lipectomized rats can lead to overproduction of PCSK9. In conclusion, up-regulation of PCSK9, due to overexpression of HNF1α gene in liver of lipectomized rats and subsequently increase in circulating PCSK9 concentration lead to decrease in liver LDL-R level. This may contribute, at least in part, to an increase in the concentration of circulating cholesterol in rats with reduced fat mass. These findings provide a possible explanation for the molecular mechanism of hypercholesterolemia observed sometimes after reduction of fat mass in human.
机译:旨在检查减少脂肪量(包括脂肪营养不良和脂肪切除术)对人血清总量和LDL-胆固醇浓度的影响的研究不一致。这项研究的目的是研究大鼠部分脂肪切除术(作为人类脂肪减少的实验模型)对(1)循环总胆固醇,LDL-胆固醇+ VLDL-胆固醇和HDL-胆固醇浓度的影响,以及(2) )可能影响血清胆固醇浓度的因素,例如:(a)肝脏LDL受体水平,(b)肝脏PCSK9的表达和(c)循环PCSK9的浓度。大鼠脂肪组织量的减少导致循环总量和LDL ++ VLDL-胆固醇浓度增加,这与(a)肝脏LDL-R水平降低,(b)肝脏PCSK9表达增加和(c)增加有关与假对照组相比,循环PCSK9浓度升高。这些变化伴随着肝脏HNF1α(和HNF4α)mRNA水平的升高。 siRNA沉默HepG2细胞中的HNF1α导致PCSK9 mRNA水平降低。这表明在脂质体切除的大鼠肝脏中HNF1α基因的过表达可导致PCSK9的过量产生。总之,由于脂质化大鼠肝脏中HNF1α基因的过表达,PCSK9的上调以及随后循环PCSK9浓度的增加导致肝脏LDL-R水平降低。这可能至少部分地导致脂肪量减少的大鼠中循环胆固醇浓度的增加。这些发现为有时在人体脂肪减少后观察到的高胆固醇血症的分子机制提供了可能的解释。

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