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Different mechanisms of cis-9,trans-11- and trans-10,cis-12- conjugated linoleic acid affecting lipid metabolism in 3T3-L1 cells

Jia-jie Zhaiac, Zhao-liang Liub, Jie-mei Lic, Jian-Ping Chend, Lin Jiangc, Dong-mei Wangc, Jin Yuana, Jian-Gang Shend, De-Po YangcCorresponding Author Informationemail address, Jia-Qi ChenaCorresponding Author Informationemail address

Received 10 November 2008; received in revised form 28 February 2009; accepted 21 September 2009. published online 08 February 2010.
Corrected Proof

Abstract 

Conjugated linoleic acid (CLA) has been shown to reduce body fat mass in various experimental animals. It is valuable to identify its influence on enzymes involved in energy expenditure, apoptosis, fatty acid oxidation and lipolysis. We investigated isomer-specific effects of high dose, long treatment of CLA (75.4 μmol/L, 8 days) on protein and gene expression of these enzymes in cultured 3T3-L1 cells. Proteomics identified significant up- or down-regulation of 52 proteins by either CLA isomer. Protein and gene expression of uncoupling protein (UCP) 1, UCP3, perilipin and peroxisome proliferator-activated receptor (PPAR) α increased whereas UCP2 reduced for both CLA isomers. And eight-day treatment of trans-10,cis-12 CLA, but not cis-9,trans-11 CLA, significantly up-regulated protein and mRNA levels of PKA (P<.05), CPT-1 and TNF-α (P<.01). Compared to protein expression, both isomers did not significantly influence the mRNA expression of HSL, ATGL, ACO and leptin. In conclusion, high-dose, long treatment of cis-9,trans-11 CLA did not promote apoptosis, fatty acid oxidation and lipolysis in adipocytes, but may induce an increase in energy expenditure. trans-10,cis-12 CLA exhibited greater influence on lipid metabolism, stimulated adipocyte energy expenditure, apoptosis and fatty acid oxidation, but its effect on lipolysis was not obvious.

a State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yatsen University, Guangzhou 510060, China

b Chemical Industry and Ecology Institute, North University of China

c Laboratory of Pharmacognosy and Natural Medicinal Chemistry, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510080, China

d School of Chinese Medicine, University of Hong Kong SAR

Corresponding Author InformationCorresponding author.

PII: S0955-2863(09)00207-1

doi:10.1016/j.jnutbio.2009.09.007

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