期刊论文详细信息
Lipids in Health and Disease
Removal from the plasma of the free and esterified forms of cholesterol and transfer of lipids to HDL in type 2 diabetes mellitus patients
Antonio C Lerario2  Bernardo L Wajchenberg2  Marina P Bertato2  Raul C Maranhão1  Carolina P Oliveira2 
[1] Instituto do Coração do HC-FMUSP, Av Dr. Enéas de Carvalho Aguiar, 44, CEP- 05423-000, São Paulo, SP, Brazil;Endocrinology Service of the Medical School Hospital, University of Sao Paulo, São Paulo, Brazil
关键词: Emulsion;    Nanoparticles;    Lipid transfer;    High density lipoprotein;    Low density lipoprotein;    Lipoprotein;    Type 2 diabetes mellitus;   
Others  :  1160295
DOI  :  10.1186/1476-511X-11-65
 received in 2012-02-03, accepted in 2012-04-11,  发布年份 2012
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【 摘 要 】

Background

The aim was to investigate new markers for type 2 diabetes (T2DM) dyslipidemia related with LDL and HDL metabolism. Removal from plasma of free and esterified cholesterol transported in LDL and the transfer of lipids to HDL are important aspects of the lipoprotein intravascular metabolism. The plasma kinetics (fractional clearance rate, FCR) and transfers of lipids to HDL were explored in T2DM patients and controls, using as tool a nanoemulsion that mimics LDL lipid structure (LDE).

Results

14C- cholesteryl ester FCR of the nanoemulsion was greater in T2DM than in controls (0.07 ± 0.02 vs. 0.05 ± 0.01 h-1, p = 0.02) indicating that LDE was removed faster, but FCR 3 H- cholesterol was equal in both groups. Esterification rates of LDE free-cholesterol were equal. Cholesteryl ester and triglyceride transfer from LDE to HDL was greater in T2DM (4.2 ± 0.8 vs. 3.5 ± 0.7%, p = 0.03 and 6.8 ± 1.6% vs. 5.0 ± 1.1, p = 0.03, respectively). Phospholipid and free cholesterol transfers were not different.

Conclusions

The kinetics of free and esterified cholesterol tended to be independent in T2DM patients and the lipid transfers to HDL were also disturbed. These novel findings may be related with pathophysiological mechanisms of diabetic macrovascular disease.

【 授权许可】

   
2012 Oliveira et al.; licensee BioMed Central Ltd.

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