Metabolism of plasma cholesterol and lipoprotein parameters are related to a higher degree of insulin sensitivity in high HDL-C healthy normal weight subjects
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Citações na Scopus
15
Tipo de produção
article
Data de publicação
2013
Título da Revista
ISSN da Revista
Título do Volume
Editora
BIOMED CENTRAL LTD
Autores
PANZOLDO, Natalia B.
ZAGO, Vanessa S.
PARRA, Eliane S.
JAUHIAINEN, Matti
FARIA, Eliana C. de
Citação
CARDIOVASCULAR DIABETOLOGY, v.12, article ID 173, 7p, 2013
Resumo
Background: We have searched if plasma high density lipoprotein-cholesterol (HDL-C) concentration interferes simultaneously with whole-body cholesterol metabolism and insulin sensitivity in normal weight healthy adult subjects. Methods: We have measured the activities of several plasma components that are critically influenced by insulin and that control lipoprotein metabolism in subjects with low and high HDL-C concentrations. These parameters included cholesteryl ester transfer protein (CETP), phospholipid transfer protein (PLTP), lecithin cholesterol acyl transferase (LCAT), post-heparin lipoprotein lipase (LPL), hepatic lipase (HL), pre-beta-1HDL, and plasma sterol markers of cholesterol synthesis and intestinal absorption. Results: In the high-HDL-C group, we found lower plasma concentrations of triglycerides, alanine aminotransferase, insulin, HOMA-IR index, activities of LCAT and HL compared with the low HDL-C group; additionally, we found higher activity of LPL and pre-beta-1HDL concentration in the high-HDL-C group. There were no differences in the plasma CETP and PLTP activities. Conclusions: These findings indicate that in healthy hyperalphalipoproteinemia subjects, several parameters that control the metabolism of plasma cholesterol and lipoproteins are related to a higher degree of insulin sensitivity.
Palavras-chave
Insulin resistance, HDL-C concentration, Lipoprotein lipases, Lecithin cholesterol acyl transferase, Pre-beta1 HDL, Plasma cholesterol metabolism markers, Cholesteryl ester transfer protein, Phospholipid transfer protein
Referências
- Assmann G, 2007, EUR J CARDIOV PREV R, V14, P208, DOI 10.1097/HJR.0b013e3280148201
- Boronat M, 2012, CARDIOVASC DIABETOL, V11, DOI 10.1186/1475-2840-11-81
- Brunham LR, 2008, J CLIN INVEST, V118, P403, DOI 10.1172/JCI33296
- Brunham LR, 2007, NAT MED, V13, P340, DOI 10.1038/nm1546
- Calabresi L, 2011, J LIPID RES, V52, P1569, DOI 10.1194/jlr.P014977
- Coniglio RI, 2012, CLIN BIOCHEM, V45, P566, DOI 10.1016/j.clinbiochem.2012.02.005
- Daimon M, 2005, BIOCHEM BIOPH RES CO, V329, P205, DOI 10.1016/j.bbrc.2005.01.119
- de Vries Rindert, 2003, Clin Lab, V49, P601
- de Vries R, 2011, ATHEROSCLEROSIS, V217, P253, DOI 10.1016/j.atherosclerosis.2011.03.021
- DOBIASOVA M, 1992, J LIPID RES, V33, P1411
- Drew BG, 2009, CIRCULATION, V119, P2103, DOI 10.1161/CIRCULATIONAHA.108.843219
- Dullaart RPF, 2008, J CLIN ENDOCR METAB, V93, P4860, DOI 10.1210/jc.2008-1213
- Duvillard L, 2013, ARTERIOSCL THROM VAS, V33, P2460, DOI 10.1161/ATVBAHA.113.301597
- Ehnholm C, 1986, Methods Enzymol, V129, P716
- Eriksson JW, 2003, ATHEROSCLEROSIS, V166, P359, DOI 10.1016/S0021-9150(02)00366-0
- FRIEDEWA.WT, 1972, CLIN CHEM, V18, P499
- Fryirs MA, 2010, ARTERIOSCL THROM VAS, V30, P1642, DOI 10.1161/ATVBAHA.110.207373
- Huang YF, 2013, CARDIOVASC DIABETOL, V12, DOI 10.1186/1475-2840-12-17
- HUTTUNEN JK, 1976, CLIN SCI MOL MED, V50, P249
- Jacobs M, 2011, METABOLISM, V60, P969, DOI 10.1016/j.metabol.2010.09.006
- Jauhiainen M, 2005, METHODS, V36, P97, DOI 10.1016/j.ymeth.2004.11.006
- Khera AV, 2011, NEW ENGL J MED, V364, P127, DOI 10.1056/NEJMoa1001689
- Knopp RH, 2003, ARTERIOSCL THROM VAS, V23, P1437, DOI 10.1161/01.ATV.0000082461.77557.C7
- Kontush A, 2006, PHARMACOL REV, V58, P342, DOI 10.1124/pr.58.3.1
- Koseki M, 2009, J ATHEROSCLER THROMB, V16, P292
- Leanca CC, 2013, NUTR METAB CARDIOVAS, V23, P279, DOI 10.1016/j.numecd.2012.12.003
- Li LX, 2011, J BIOL CHEM, V286, P17809, DOI 10.1074/jbc.M110.180893
- MIETTINEN TA, 1982, CLIN CHIM ACTA, V124, P245, DOI 10.1016/0009-8981(82)90393-X
- Nunes VS, 2011, CLIN CHIM ACTA, V412, P176, DOI 10.1016/j.cca.2010.09.039
- Paramsothy P, 2011, AM J CLIN NUTR, V94, P1182, DOI 10.3945/ajcn.110.006668
- Povel CM, 2011, MOL GENET METAB, V104, P666, DOI 10.1016/j.ymgme.2011.08.035
- Praveen EP, 2011, HORM-INT J ENDOCRINO, V10, P57
- Quintao ECR, 2010, ATHEROSCLEROSIS, V209, P1, DOI 10.1016/j.atherosclerosis.2009.08.002
- Rashid S, 2003, CLIN BIOCHEM, V36, P421, DOI 10.1016/S0009-9120(03)00078-X
- Riemens SC, 2001, SCAND J CLIN LAB INV, V61, P1
- Robciuc MR, 2013, ARTERIOSCL THROM VAS, V33, P1706, DOI 10.1161/ATVBAHA.113.301397
- Salah A, 2009, J CRIT CARE, V24, DOI 10.1016/j.jcrc.2009.06.005
- Saleheen D, 2006, INT J CARDIOL, V110, P259, DOI 10.1016/j.ijcard.2005.06.059
- Sethi AA, 2010, CLIN CHEM, V56, P1128, DOI 10.1373/clinchem.2009.139931
- Simonen PP, 2002, DIABETES CARE, V25, P1511, DOI 10.2337/diacare.25.9.1511
- Stahlman M, 2013, BBA-MOL CELL BIOL L, V1831, P1609, DOI 10.1016/j.bbalip.2013.07.009
- Vergeer M, 2010, DIABETES CARE, V33, P869, DOI 10.2337/dc09-1562
- Villarreal-Molina MT, 2008, DIABETES, V57, P509, DOI 10.2337/db07-0484
- von Eckardstein A, 2011, CURR OPIN LIPIDOL, V22, P26, DOI 10.1097/MOL.0b013e3283412279
- Weingartner O, 2011, CHEM PHYS LIPIDS, V164, P451, DOI 10.1016/j.chemphyslip.2011.03.008
- Welch CL, 2001, P NATL ACAD SCI USA, V98, P7946, DOI 10.1073/pnas.141239098
- Xiao CT, 2008, CIRC RES, V103, P159, DOI 10.1161/CIRCRESAHA.108.178756