1997
DOI: 10.1016/s0005-2760(96)00138-5
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Thia fatty acids, metabolism and metabolic effects

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Cited by 77 publications
(56 citation statements)
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“…A PPAR-alpha targeted promoter has been discovered 5′upstream to the PANK1 gene [81]. PPAR-alpha receptors are transcription factors that are stimulated by increased (among other things) intracellular lipids/fatty acids; the function of PPAR-alpha is thought to involve decreasing intracellular FA stores (FAs) [82][83][84][85][86]. These results suggest that miR-103/7 acts symbiotically with the PANK proteins and the PPAR-alpha pathway, by decreasing FA syntheses and uptake (by inhibiting FASN, ACOX1, and others), and increasing the activity of the pyruvate dehydrogenase complex (by inhibiting PDK4, PISD, and PDPR).…”
Section: Bioinformatics Predict a Role For Mir-103/mir-107 Paralogs Imentioning
confidence: 99%
“…A PPAR-alpha targeted promoter has been discovered 5′upstream to the PANK1 gene [81]. PPAR-alpha receptors are transcription factors that are stimulated by increased (among other things) intracellular lipids/fatty acids; the function of PPAR-alpha is thought to involve decreasing intracellular FA stores (FAs) [82][83][84][85][86]. These results suggest that miR-103/7 acts symbiotically with the PANK proteins and the PPAR-alpha pathway, by decreasing FA syntheses and uptake (by inhibiting FASN, ACOX1, and others), and increasing the activity of the pyruvate dehydrogenase complex (by inhibiting PDK4, PISD, and PDPR).…”
Section: Bioinformatics Predict a Role For Mir-103/mir-107 Paralogs Imentioning
confidence: 99%
“…TTA cannot be β-oxidized due to the position of the sulfur in the carbon chain and thus it is metabolized in mammals via ω-hydroxylation in the endoplasmic reticulum followed by peroxisomal oxidation from the ω-end producing short chain sulfoxy dicarboxylic acids (Skrede et al, 1997). In mammals, TTA increases both liver and muscle mitochondrial and peroxisomal fatty acid oxidation, decreases plasma lipids and adipose tissue mass, and increases free fatty acid transport from peripheral tissues to liver (Berge et al, 2002).…”
Section: Introductionmentioning
confidence: 99%
“…8 Skrede et al have reviewed the metabolism of thia fatty acids. 9 Our group have synthesized and studied spectroscopic and mass spectrometric properties of the positional isomers of the methyl thialaurate, [10][11][12][13] ten methyl dithiastearate isomers 14 and the corresponding sulfinyl and sulfonyl derivatives of methyl thialaurate. 15 In this paper, we describe the synthesis of a set of positional isomers of C 18 acetylenic thia fatty esters (5-8, Scheme 1) in an effort to study the effect of the sulfur atom on the chemical shifts of the carbon nuclei in the alkynyl chain of these thia fatty ester isomers by nuclear magnetic resonance spectroscopy.…”
Section: Introductionmentioning
confidence: 99%