Literature DB >> 22009636

Lipoprotein lipase deficiency in chronic kidney disease is accompanied by down-regulation of endothelial GPIHBP1 expression.

Nosratola D Vaziri1, Jun Yuan, Zhenmin Ni, Susanne B Nicholas, Keith C Norris.   

Abstract

BACKGROUND: Chronic renal failure (CRF) is associated with hypertriglyceridemia and impaired clearance of very low density lipoprotein (VLDL) and chylomicrons which are largely due to lipoprotein lipase (LPL) deficiency/dysfunction. After its release from myocytes and adipocytes, LPL binds to the endothelium in the adjacent capillaries where it catalyzes hydrolysis of triglycerides in VLDL and chylomicrons. The novel endothelium-derived molecule, glycosylphosphatidylinositol-anchored binding protein 1 (GPIHBP1), plays a critical role in LPL metabolism and function by anchoring LPL to the endothelium and binding chylomicrons. GPIHBP1-deficient mice and humans exhibit severe hypertriglyceridemia and diminished heparin-releasable LPL, pointing to the critical role of GPIHBP1 in regulation of LPL activity. Given its central role in regulation of LPL activity and triglyceride metabolism, we explored the effect of chronic kidney disease (CKD) on GPIHBP1 expression.
METHODS: Expression of GPIHBP1 and LPL were determined by reverse transcriptase-polymerase chain reaction, Western blot and immunohistochemical analyses in the adipose tissue, skeletal muscle and myocardium of rats 12 weeks after 5/6 nephrectomy (CRF) or sham-operation (control).
RESULTS: Compared to the controls, the CRF group exhibited severe hypertriglyceridemia, significant reduction of the skeletal muscle, myocardium and adipose tissue LPL mRNA and protein abundance. This was accompanied by parallel reductions of GPIHBP1 mRNA abundance and immunostaining in the tested tissues.
CONCLUSIONS: LPL deficiency in CKD is associated with and compounded by GPIHBP1 deficiency. Together these abnormalities contribute to impaired clearance of triglyceride-rich lipoproteins, diminished availability of lipid fuel for energy storage in adipocytes and energy production in myocytes and consequent hypertriglyceridemia, cachexia, muscle weakness and atherosclerosis.

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Year:  2011        PMID: 22009636      PMCID: PMC3417131          DOI: 10.1007/s10157-011-0549-3

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


  25 in total

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Journal:  Kidney Int       Date:  1994-02       Impact factor: 10.612

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Authors:  Nosratola D Vaziri; Keith Norris
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  18 in total

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3.  Impaired postprandial lipemic response in chronic kidney disease.

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Review 4.  Disorders of lipid metabolism in nephrotic syndrome: mechanisms and consequences.

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Review 5.  Residual Cardiovascular Risk in Chronic Kidney Disease: Role of High-density Lipoprotein.

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Journal:  Arch Med Res       Date:  2015-05-23       Impact factor: 2.235

Review 6.  Dyslipidaemia in nephrotic syndrome: mechanisms and treatment.

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Review 7.  Lipoprotein metabolism and CKD: overview.

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Review 8.  Statins in the management of dyslipidemia associated with chronic kidney disease.

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10.  Dysregulation of hepatic fatty acid metabolism in chronic kidney disease.

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