|
Originally published In Press as doi:10.1194/jlr.M600050-JLR200 on October 2, 2006
Journal of Lipid Research, Vol. 48, 77-85, January 2007
Copyright © 2007 by American Society for Biochemistry and Molecular Biology
Metabolism of phytol to phytanic acid in the mouse, and the role of PPAR in its regulation
J. Gloerich,
D. M. van den Brink,
J. P. N. Ruiter,
N. van Vlies,
F. M. Vaz,
R. J. A. Wanders and
S. Ferdinandusse1
Laboratory of Genetic Metabolic Diseases, Departments of Clinical Chemistry and Pediatrics, Emma's Children's Hospital, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands
Published, JLR Papers in Press, October 2, 2006.
1 To whom correspondence should be addressed. e-mail: s.ferdinandusse{at}amc.uva.nl
Phytol, a branched-chain fatty alcohol, is the naturally occurring precursor of phytanic and pristanic acid, branched-chain fatty acids that are both ligands for the nuclear hormone receptor peroxisome proliferator-activated receptor (PPAR ). To investigate the metabolism of phytol and the role of PPAR in its regulation, wild-type and PPAR knockout (PPAR /) mice were fed a phytol-enriched diet or, for comparison, a diet enriched with Wy-14,643, a synthetic PPAR agonist. After the phytol-enriched diet, phytol could only be detected in small intestine, the site of uptake, and liver. Upon longer duration of the diet, the level of the (E)-isomer of phytol increased significantly in the liver of PPAR / mice compared with wild-type mice. Activity measurements of the enzymes involved in phytol metabolism showed that treatment with a PPAR agonist resulted in a PPAR -dependent induction of at least two steps of the phytol degradation pathway in liver. Furthermore, the enzymes involved showed a higher activity toward the (E)-isomer than the (Z)-isomer of their respective substrates, indicating a stereospecificity toward the metabolism of (E)-phytol. In conclusion, the results described here show that the conversion of phytol to phytanic acid is regulated via PPAR and is specific for the breakdown of (E)-phytol.
Supplementary key words peroxisome proliferator-activated receptor fatty aldehyde dehydrogenase branched-chain fatty acids Abbreviations: FALDH, fatty aldehyde dehydrogenase; MBP, maltose binding protein; MTBSTFA, N-methyl-N-(tert-butyldimethylsilyl)trifluoroacetamide; PPAR , peroxisome proliferator-activated receptor 

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
D. Demozay, J.-C. Mas, S. Rocchi, and E. Van Obberghen
FALDH Reverses the Deleterious Action of Oxidative Stress Induced by Lipid Peroxidation Product 4-Hydroxynonenal on Insulin Signaling in 3T3-L1 Adipocytes
Diabetes,
May 1, 2008;
57(5):
1216 - 1226.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Ashibe, T. Hirai, K. Higashi, K. Sekimizu, and K. Motojima
Dual Subcellular Localization in the Endoplasmic Reticulum and Peroxisomes and a Vital Role in Protecting against Oxidative Stress of Fatty Aldehyde Dehydrogenase Are Achieved by Alternative Splicing
J. Biol. Chem.,
July 13, 2007;
282(28):
20763 - 20773.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 2007 by the American Society for Biochemistry and Molecular Biology.
|
Advertisement
Advertisement
|