2016
DOI: 10.1186/s12986-016-0075-0
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Short chain acyl-CoA dehydrogenase deficiency and short-term high-fat diet perturb mitochondrial energy metabolism and transcriptional control of lipid-handling in liver

Abstract: BackgroundThe liver is an important site of fat oxidation, which participates in the metabolic regulation of food intake. We showed previously that mice with genetically inactivated Acads, encoding short-chain acyl-CoA dehydrogenase (SCAD), shift food consumption away from fat and toward carbohydrate when tested in a macronutrient choice paradigm. This phenotypic eating behavior suggests a link between fat oxidation and nutrient choice which may involve an energy sensing mechanism. To identify hepatic processe… Show more

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Cited by 15 publications
(11 citation statements)
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References 46 publications
(62 reference statements)
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“…Mice were acclimated to constant dark for 6 weeks, and livers were harvested at 9:00 am (CT1), and then every 4 h, (CT5, CT9, CT13, CT17, and CT21) for 6 time-points. RNA-Seq data was presented as reads count of pooled samples [39]. For these selected genes, RT-qPCR verified their rhythms and confirmed the MetaCycle results.…”
Section: Discussionsupporting
confidence: 56%
See 1 more Smart Citation
“…Mice were acclimated to constant dark for 6 weeks, and livers were harvested at 9:00 am (CT1), and then every 4 h, (CT5, CT9, CT13, CT17, and CT21) for 6 time-points. RNA-Seq data was presented as reads count of pooled samples [39]. For these selected genes, RT-qPCR verified their rhythms and confirmed the MetaCycle results.…”
Section: Discussionsupporting
confidence: 56%
“…On the contrary, the periods of Lipin1 and Lipin2 were increased under L-DD. Stearoyl-Coenzyme A desaturase (Scd) genes encode the key enzymes involved in the conversion of saturated fatty acids into monounsaturated fatty acids [39]. L-DD decreased the period of Scd1 and Scd2.…”
Section: Resultsmentioning
confidence: 99%
“…Several genes that are cis -regulated in the muscle participate in lipid or carbohydrate metabolism, e.g. HIV-1 Tat Interactive Protein 2 ( HTATIP2 ) [14], exocyst complex component 7 ( EXOC7 ) [15] acyl-CoA dehydrogenase short chain ( ACADS ) [16], insulin degrading enzyme ( IDE ) [17], solute carrier family 38 member 9 ( SLC38A9 ) [18], and family with sequence similarity 3 member C ( FAM3C ) [19]. With regard to the liver, hydroxysteroid dehydrogenase like 2 ( HSDL2 ) [20] and lipase A ( LIPA ) [21] genes have also important roles in lipid metabolism.…”
Section: Resultsmentioning
confidence: 99%
“…Studies have shown that macrophage activation stimulated by LPS promotes an increase in glucose uptake and glycolysis, giving preference to this pathway to supply the energy demand of pro-inflammatory processes 44 . Fatty acids degradation was also overrepresented for turquoise module, and this is an important energy production pathway, especially for tissues that have a high metabolic demand, such as the liver, the main organ for homeostasis regulation in mammals 45 . Fatty acids are released from adipose tissue and absorbed by hepatocytes where they will be oxidized to ATP production, which will act as energy source or converted into lipid molecules and derivatives 46 .…”
Section: Discussionmentioning
confidence: 99%