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             Publication
Journal Publication
Research Title Effects of Oleic Acid and Palmitic Acid on the Expression of Lipid-Biotransformation-Related Genes  
Date of Distribution 17 March 2018 
Conference
     Title of the Conference The 10th Annual Northeast Pharmacy Research Conference of 2018 
     Organiser Khon Kaen University 
     Conference Place Faculty of Pharmaceutical Science 
     Province/State Khon Kaen, Thailand 
     Conference Date 17 March 2018 
     To 18 March 2018 
Proceeding Paper
     Volume
     Issue
     Page 157 
     Editors/edition/publisher
     Abstract Introduction: Oleic acid (OA) and palmitic acid (PA) are saturated and unsaturated fatty acid, respectively, that mostly found in daily dietary especially western fried food. CYP4A11 is one of cytochrome P450s mainly responsible for ωω-1 hydroxylation in fatty acid metabolism.Some evidences have suggested that human CYP4A11 expression is related to peroxisome proliferator activated receptor alpha (PPAR-α). Moreover, OATP1B1, a well-known transporter, commonly expresses in the basolateral membrane of hepatocytes. However, regulatory pathway of fatty acid is unclear. Human hepatocellular carcinoma cell (HepG2), human choriocarcinoma cell (BeWo), and human colorectal adenocarcinoma cell (Caco-2) are extensively used as models for study of xenobiotics/nutrients-metabolism. Hence, the effects of OA and PA on these lipid-biotransformation-related genes, namely, OATP1B1, CYP4A11, and PPAR-α, were determined in three cell lines. Materials and methods: OA or PA at the final concentration of 1 mM (in 0.5%isopropanol) was incubated with HepG2, BeWo, and CaCo2 cells (5x10 5 cells/mL in 6-well plate) for 24 h. Then, total RNA was isolated using acid guanidinium thiocyanate-phenol-chloroform method. Expressions of OATP1B1, CYP4A11, and PPAR-α mRNA were determined using RT-qPCR. Results: The expression of OATP1B1 mRNA was low abundant in BeWo and unchanged by either OA or PA. OA markedly induced the expression of OATP1B1 in HepG2 and CaCo2 while PA did not. The expression of CYP4A11 mRNA was higher abundant in HepG2 than BeWo. Interestingly, both OA and PA significantly induced the level of CYP4A11 mRNA in BeWo but not in HepG2. PPAR-α was not modified by either OA or PA in HepG2 whilst PA extensively induced PPAR-α in BeWo. Conclusion: OA and PA might have different biotransformation. Moreover, organ-represented cell lines demonstrated different regulatory pathways of lipid metabolism. 
Author
605150051-6 Miss NAWARATT [Main Author]
Pharmaceutical Sciences Master's Degree

Peer Review Status มีผู้ประเมินอิสระ 
Level of Conference ชาติ 
Type of Proceeding Abstract 
Type of Presentation Poster 
Part of thesis true 
Presentation awarding false 
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