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A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARα-dependent and -independent pathways
被引:58
作者:
Gloerich, J
van Vlies, N
Jansen, GA
Denis, S
Ruiter, JPN
van Werkhoven, MA
Duran, M
Vaz, FM
Wanders, RJA
Ferdinandusse, S
[1
]
机构:
[1] Univ Amsterdam, Acad Med Ctr, Dept Clin Chem, Lab Genet Metab Dis, NL-1100 DE Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Pediat, Lab Genet Metab Dis, NL-1100 DE Amsterdam, Netherlands
关键词:
peroxisome proliferator-activated receptor alpha;
peroxisomes;
mitochondria;
fatty acid beta-oxidation;
very long-chain fatty acids;
branched-chain fatty acids;
acylcarnitines;
peroxisomal disorders;
D O I:
10.1194/jlr.M400337-JLR200
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Branched-chain fatty acids (such as phytanic and pristanic acid) are ligands for the nuclear hormone receptor peroxisome proliferator-activated receptor alpha (PPAR alpha) in vitro. To investigate the effects of these physiological compounds in vivo, wild-type and PPAR alpha-deficient (PPAR alpha(-/-)) mice were fed a phytol-enriched diet. This resulted in increased plasma and liver levels of the phytol metabolites phytanic and pristanic acid. In wild-type mice, plasma fatty acid levels decreased after phytol feeding, whereas in PPAR alpha(-/-) mice, the already elevated fatty acid levels increased. In addition, PPAR alpha(-/-) mice were found to be carnitine deficient in both plasma and liver. Dietary phytol increased liver free carnitine in wild-type animals but not in PPAR alpha(-/-) mice. Investigation of carnitine biosynthesis revealed that PPAR alpha is likely involved in the regulation of carnitine homeostasis. Furthermore, phytol feeding resulted in a PPAR alpha-dependent induction of various peroxisomal and mitochondrial beta-oxidation enzymes. In addition, a PPAR alpha-independent induction of catalase, phytanoyl-CoA hydroxylase, carnitine octanoyltransferase, peroxisomal 3-ketoacyl-CoA thiolase, and straight-chain acyl-CoA oxidase was observed. In conclusion, branched-chain fatty acids are physiologically relevant ligands of PPAR alpha in mice. These findings are especially relevant for disorders in which branched-chain fatty acids accumulate, such as Refsum disease and peroxisome biogenesis disorders.
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页码:716 / 726
页数:11
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