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adult male CD1 mice to BPA (0, 5, 50, 500, and 5000 μg/kg per day) resulted in the accumulation of hepatic triglycerides (TGs) and cholesteryl esters (CHOL), changes in hepatic free fatty acid (FFA) composition as well as upregulation of genes involved
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? ? ? The thioesterase multidomain proteins STARD14 ACOT11_v2, BFIT2 Brown adipose tissue † Cytosolic c ? Fatty acid d (?) Medium chain fatty-acyl-coA hydrolysis 10 STARD15 ACOT12 Liver † Cytosolic c ? Acetyl-coA hydrolysis 11 StAR, steroidogenic acute
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intracellular Ca 2 + levels. Ghrelin has a unique fatty acid modification on its N-terminal end as a result of the activity of the ghrelin O -acyltransferase enzyme ( Yang et al . 2008 ). However, the majority of circulating ghrelin is actually lacking this
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Yutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan
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Yutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan
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Yutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan
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Yutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan
Division of Molecular and Metabolic Medicine, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Kobe, Japan
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Introduction Carbohydrate response element-binding protein (ChREBP) is critical for regulation of fatty acid and triglyceride synthesis in the liver ( Iizuka 2017 ). ChREBP has two isoforms, ChREBP-α ( Chrebpa ) and ChREBP-β ( Chrebpb
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-acclimated for 60 min and horizontal locomotor activity was quantified for 60 min. Plasma measurements Plasma triglyceride (TG) was measured using a glycerol phosphate oxidase-Trinder TG kit (Sigma). Plasma free fatty acid (FFA) and glycerol were measured using a
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characterized by high body fat mobilization. This suggests that, in addition to its role in preventing starvation, ghrelin exerts a prominent role in the regulation of fat metabolism. For example, feeding rumen-protected long-chain fatty acids increases the
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status between the mouse and hamster adrenals, we evaluated the expression of a few core genes involved in the regulation of these processes. We found that Cpt1a , a transferase essential for mitochondrial fatty acid oxidation (FAO), was substantially
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hypothesized that an increased de novo lipogenesis after fructose intake in parallel with a decreased fatty acid oxidation leads to hepatic fat deposition. ACC, acetyl-CoA-carboxylase; ATP, adenosine triphosphate; CPT1a, carnitine palmitoyltransferase 1A; FA
Pinnacle Clinical Research, Live Oak, USA
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Baylor College of Medicine, Houston, USA
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the adult AMDR is a suggested intake of linoleic acid at 12–17 g/day and α-linolenic acid at 1.1–1.6 g/day, both of which are essential fatty acids and thus, cannot be synthesized innately but only obtained through the diet. High-fat diets (HFD
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gluconeogenesis (the generation of glucose from non-carbohydrate substrates), and free fatty acids, which decrease insulin sensitivity by inhibiting intracellular insulin signaling and glucose uptake, are increased in the circulation, contributing to continuation