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Effects of n-3 and n-6 fatty acids on the cholesteryl ester transfer protein (CETP) expression and activity in transgenic mice

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Author(s):
Helena Fonseca Raposo
Total Authors: 1
Document type: Doctoral Thesis
Press: Campinas, SP.
Institution: Universidade Estadual de Campinas (UNICAMP). Instituto de Biologia
Defense date:
Examining board members:
Helena Coutinho Franco de Oliveira; Edna Regina Nakandakare; Maria Isabel Cardoso Alonso Vale; Marcio Alberto Torsoni; Luiz Carlos Carvalho Navegantes
Advisor: Helena Coutinho Franco de Oliveira
Abstract

Cholesteryl ester transfer protein (CETP) is a plasma protein that mediates the exchange of triglycerides for esterified cholesterol from HDL to the apoB containing lipoproteins. In this way, CETP promotes reduction of plasma HDLcholesterol and, thus, increases the risk of atherosclerosis. Recently, we found that CETP expressing mice (CETP-Tg) presented less adipose tissue mass than nonexpressing controls. In this work we investigated possible mechanisms to explain these findings. CETP-Tg and non-transgenic (NTg) control mice (C57/BL6 background) were fed with chow diet from weaning to 5 month of age. CETP-Tg mice had reduced visceral and subcutaneous fat depots (~30%) that was not compensated by lipid ectopic deposition and could not be explained by differences in fat intake and excretion. Lipogenesis rates in vivo and in isolated adipocytes (estimated using 3H2O and 14C-acetate) were similar in both CETP-Tg and control mice. Lipid retention and glucose uptake by liver, muscle and adipose tissues (estimated after an oral dose of 3H-triolein and IP injection of 3H-deoxiglucose) showed no significant differences between groups. In the fed state, CETP group showed higher (~50%) basal lipolysis rates in vivo and in isoproterenol stimulated lipolysis rates in isolated adipocytes. In accordance, visceral adipose hormone sensitive lipase (HSL) and adipose triglyceride lipase (ATGL) mRNA expression were elevated, as well as fatty acid transport protein (FATP1). In brown adipose tissue, ATGL, FATP1 and uncoupling protein 1 (UCP1) were increased. Furthermore, beta 3 adrenergic receptor proteins mass were upregulated in visceral and brown adipose tissues membrane extracts. In addition, whole body energy expenditure (measured by respirometry) was found to be elevated in CETP-Tg mice (10%). In conclusion, CETP change expression and function of proteins related to lipolysis and thermogeneis, thus, increasing whole body energy expenditure and resulting in less body fat content. These findings disclose a novel anti-adipogenic role for CETP (AU)