Rat lipoprotein lipase,LPL ELISA Kit

1. The results of the present study indicated that maternal undernutrition during pregnancy may lead to an increase in hepatic triglycerides, via alterations in the transcriptional and epigenetic regulation of the LPL gene. PMID: 27035287
2. Cardiomyocyte VEGF activates EC Notch signaling, facilitating GPIHBP1-mediated translocation of LPL across EC and regulating LPL-derived fatty acid delivery to the cardiomyocytes. PMID: 26586663
3. the amount of LPL expressed in muscle and heart governed both the binding of chylomicron particles and the assimilation of chylomicron lipids in the tissue. PMID: 25589507
4. Data indicate that oxidation of oleic acid was reduced by 50% in lipoprotein lipase LPL-knock-down (LPL-KD) cells compared to wild-type (WT) cells. PMID: 25931001
5. Activated cyclin-dependent kinase 5 promotes microglial phagocytosis of fibrillar beta-amyloid by up-regulating lipoprotein lipase expression PMID: 23816988
6. Suggest that the heparanase-lipoprotein lipase-VEGF axis amplifies fatty acid delivery, a rapid and adaptive mechanism that is geared to overcome the loss of glucose consumption by the diabetic heart. PMID: 24115032
7. The plasticity of the LPL system is severely blunted or completely lost in insulin resistant rats. PMID: 23176178
8. active heparanase released lipoprotein lipase from the myocyte surface PMID: 23471235
9. Data suggest that endothelial lipoprotein lipase (LPL) levels in the heart are altered to maintain FA flux and may exploit angiopoietin-like protein-4 (ANGPTL4). PMID: 22226882
10. Report a simple procedure for measuring lipoprotein lipase activity. PMID: 22870821
11. In acute hyperglycemia and moderate diabetes, exaggerated LPL processing to dimeric, catalytically active enzyme increases coronary LPL, delivering more FA to the heart when glucose utilization is compromised. PMID: 21646389
12. This study showed that adiponectin mediates actin cytoskeleton remodeling to translocate lipoprotein lipase and allow subsequent activation. PMID: 21147877
13. When compared with obesity-resistant rats, the gene expression of LPL was higher in obesity-prone rats. PMID: 17712951
14. The over-expression of LPL in the hippocampus may play an important role in the oxidative stress mechanisms following status epilepticus (SE) by regulating the uptake of vitamin E. PMID: 20497648
15. Down-regulation of adipose tissue lipoprotein lipase during fasting requires that a gene, separate from the lipase gene, is switched on PMID: 11809775
16. An HFS diet induces changes in LPL and VLDL-R in a manner which favors shunting of dietary fat from skeletal muscle to adipose tissue. PMID: 11882325
17. characterized changes in LPL activity in adipose tissue and muscles before and during the early phase of obesity development in the JCR:LA-cp rat PMID: 11896485
18. STZ-induced diabetes causes a decrease in LPL activity in the sciatic nerve that is reversible with insulin treatment PMID: 11897675
19. insulin deficiency impairs the expression of LPL in mammary glands, revealing the role of insulin as a modulator of the enzyme at the mRNA expression level PMID: 11900280
20. The hormonal responses of LPL activity and lipolysis in adipose tissue differed depending on the stage of the estrous cycle. PMID: 12032743
21. Although Lpl increases arterial wall accumulation of triglyceride-rich particles(TGRPs), it also reduces the penetration of TGRPs into the arterial wall--a novel antiatherogenic property. PMID: 12482838
22. PPAR-gamma activation mediates adipose depot-specific effects on gene expression and activity of this enzyme. PMID: 12540599
23. the nutritional regulation of LPL in adipose tissue determines the activity state of extracellular LPL. PMID: 12551943
24. the striking sensitivity of muscle lipoprotein lipase to inactivity and low-intensity contractile activity may indicate why inactivity is a risk factor for metabolic diseases PMID: 12815182
25. Rapid "metabolic switching" occurs through Lpl occupation of endothelial binding-sites. PMID: 12967632
26. AMPK-mediated recruitment of LPL to the coronary lumen could represent an immediate compensatory response by the heart to guarantee fatty acid supply. PMID: 15328075
27. The decrease of LPL mass and activity that occurs when explants of rat adipose tissue are incubated is due to proteolysis of extracellular LPL. The effect of inhibitors indicates, but does not prove, that the degradation is mediated by MMPs. PMID: 15670333
28. Lysophosphatidic acid induced increases in cardiac lipoprotein lipase occurred via posttranscriptional mechanisms and processes. PMID: 15681706
29. Upregulated by rosiglitazone PMID: 15887043
30. Chronic stress decreased LPL in mesenteric and epididymal white adipose tissue(WAT). Acute stress decreased LPL only in retroperitoneal WAT and increased LPL in preheparin plasma active LPL. PMID: 15947029
31. The finding that nephrotic serum alters lipoprotein lipase (LpL) binding to rat aortic endothelial cells suggests LpL depletion results from decreased binding rather than defective delivery. PMID: 16807550
32. Angiopoietin-like protein 4 is a fasting-induced controller of lipoprotein lipase in adipose tissue, acting extracellularly on the native conformation in an unusual fashion, like an unfolding molecular chaperone PMID: 17088546
33. Accelerated triglyceride clearance was associated with increased Lpl activity, mostly in brown adipose tissue. PMID: 17170230
34. the release from endothelium to the bloodstream may constitute a fast nonexplored mechanism of tissue LPL activity regulation, involved in the lipid energy-substrate redistribution between tissues needed to prepare the "fight-or-flight" respo PMID: 17259660
35. hormonal and nutritional induction of liver PPAR-alpha expression around birth and its maintained elevated level throughout suckling is responsible for the induction of liver LPL-expression and activity during suckling PMID: 17451160
36. Suggest the involvement of brain phosphatidylinositol-specific PLC and diacylglycerol lipase in the centrally administered histamine-induced activation of the adrenomedullary outflow in rats. PMID: 17628524
37. oxidized fat impairs normal metabolic adaptations during lactation, which promote the utilization of metabolic substrates by the mammary gland for the synthesis of milk PMID: 17709442
38. Administration of resistin to adipocytes mimicked the effects of GIP on the PKB/LKB1/AMPK/LPL pathway: increasing phosphorylation of PKB, reducing levels of phosphorylated LKB1 and AMPK, and increasing LPL activity. PMID: 17890220
39. Recruitment of LPL to the cardiomyocyte surface represents an immediate compensatory response by the heart to guarantee fatty acid supply when glucose utilization is compromised. PMID: 17942824
40. after diabetes, Protein kinase D control of LPL requires dissociation of Hsp25 from PKCdelta, association between PKCdelta and PKD, and vesicle fission. PMID: 18583709
41. Cold acclimation significantly increased heparin-releasable LPL (P<0.05) and tissue residual LPL (P<0.01)in the heart. AMPK phosphorylation does not mediate the enhanced translocation of LPL to cardiac endothelium. PMID: 18722549
42. Epididymal white adipose tissue perfused in situ with an nitric oxide donor rapidly releases LPL from the endothelium. PMID: 19088434

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KEGG: rno:24539

STRING: 10116.ENSRNOP00000016543

UniGene: Rn.3834