Search Results
Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA
Biologic Resources Laboratory, University of Illinois at Chicago, Chicago, Illinois, USA
Search for other papers by Abigail Wolf Greenstein in
Google Scholar
PubMed
Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA
Search for other papers by Neena Majumdar in
Google Scholar
PubMed
Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA
Search for other papers by Peng Yang in
Google Scholar
PubMed
Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA
Search for other papers by Papasani V Subbaiah in
Google Scholar
PubMed
Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA
Search for other papers by Rhonda D Kineman in
Google Scholar
PubMed
Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA
Search for other papers by Jose Cordoba-Chacon in
Google Scholar
PubMed
clearance, and regulation of body fat mass . Journal of Biological Chemistry 278 34268 – 34276 . ( doi:10.1074/jbc.M300043200 ) Glatz JF Luiken JJ Bonen A 2010 Membrane fatty acid transporters as regulators of lipid metabolism
Search for other papers by Sangeeta Maity in
Google Scholar
PubMed
Search for other papers by Dipak Kar in
Google Scholar
PubMed
Search for other papers by Kakali De in
Google Scholar
PubMed
Search for other papers by Vivek Chander in
Google Scholar
PubMed
Search for other papers by Arun Bandyopadhyay in
Google Scholar
PubMed
, during cardiac hypertrophy, the energy metabolism shifts from fatty acids to glucose, much like the fetal period when mitochondrial content is low ( Barger & Kelly 2000 , Garcia & Goldenthal 2002 , Lehman & Kelly 2002 , Goffart et al . 2004 ). It was
Search for other papers by Elena Grasselli in
Google Scholar
PubMed
Search for other papers by Adriana Voci in
Google Scholar
PubMed
Dipartimento di Biologia, Dipartimento di Scienze Biologiche ed Ambientali, Istituto Nazionale Biostrutture e Biosistemi (INBB), Università di Genova, Corso Europa 26, Genova 16132, Italy
Search for other papers by Laura Canesi in
Google Scholar
PubMed
Search for other papers by Fernando Goglia in
Google Scholar
PubMed
Search for other papers by Silvia Ravera in
Google Scholar
PubMed
Search for other papers by Isabella Panfoli in
Google Scholar
PubMed
Search for other papers by Gabriella Gallo in
Google Scholar
PubMed
Dipartimento di Biologia, Dipartimento di Scienze Biologiche ed Ambientali, Istituto Nazionale Biostrutture e Biosistemi (INBB), Università di Genova, Corso Europa 26, Genova 16132, Italy
Search for other papers by Laura Vergani in
Google Scholar
PubMed
lipid homeostasis. In humans and rodents, PPARs are encoded under three isoforms α, γ, and δ that bind to free fatty acids (FFAs; Viswakarma et al . 2010 ), but only PPARα binds to saturated FFAs ( Xu et al . 1999 ). In the liver, PPARα is the master
Institute for Health and Sport (iHeS), Victoria University, Melbourne, Victoria, Australia
Search for other papers by Amanda J Genders in
Google Scholar
PubMed
Search for other papers by Timothy Connor in
Google Scholar
PubMed
Search for other papers by Shona Morrison in
Google Scholar
PubMed
Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia
Search for other papers by Simon T Bond in
Google Scholar
PubMed
Search for other papers by Brian G Drew in
Google Scholar
PubMed
Search for other papers by Peter J Meikle in
Google Scholar
PubMed
Search for other papers by Kirsten F Howlett in
Google Scholar
PubMed
Search for other papers by Sean L McGee in
Google Scholar
PubMed
,5-bisphosphate (PIP 2 ) to DG at the plasma membrane ( Rozengurt 2011 ). Nutrient substrates such as saturated fatty acids that drive de novo DG accumulation can also increase PKD phosphorylation ( Mayer et al. 2019 ). Furthermore, PKD can be activated
Search for other papers by Joëlle Dupont in
Google Scholar
PubMed
Search for other papers by Sophie Tesseraud in
Google Scholar
PubMed
Search for other papers by Michel Derouet in
Google Scholar
PubMed
Search for other papers by Anne Collin in
Google Scholar
PubMed
Search for other papers by Nicole Rideau in
Google Scholar
PubMed
Search for other papers by Sabine Crochet in
Google Scholar
PubMed
Search for other papers by Estelle Godet in
Google Scholar
PubMed
Search for other papers by Estelle Cailleau-Audouin in
Google Scholar
PubMed
Search for other papers by Sonia Métayer-Coustard in
Google Scholar
PubMed
Search for other papers by Michel J Duclos in
Google Scholar
PubMed
Search for other papers by Christian Gespach in
Google Scholar
PubMed
Search for other papers by Tom E Porter in
Google Scholar
PubMed
Search for other papers by Larry A Cogburn in
Google Scholar
PubMed
Search for other papers by Jean Simon in
Google Scholar
PubMed
Agricultural Research and Teaching. Metabolic and hormone analyses Plasma glucose levels were measured by the glucose oxidase method (Glucose Beckman Analyser 2, Beckman, Palo Alto, CA, USA). Free or non-esterified fatty acid (NEFA) levels were determined with
Search for other papers by Rohit Singhal in
Google Scholar
PubMed
Physiology and Biophysics, Arkansas Children's Nutrition Center, Departments of
Search for other papers by Kartik Shankar in
Google Scholar
PubMed
Physiology and Biophysics, Arkansas Children's Nutrition Center, Departments of
Search for other papers by Thomas M Badger in
Google Scholar
PubMed
Physiology and Biophysics, Arkansas Children's Nutrition Center, Departments of
Search for other papers by Martin J Ronis in
Google Scholar
PubMed
receptor-related receptor ( Insrr ) by 4- and 1.6-fold, while insulin receptor substrate 3 ( Irs3 ) and insulin induced gene 2 ( Insig2 ) were downregulated by 3.7- and 1.8-fold respectively. Genes involved in fatty acid metabolism and transport such as
Search for other papers by A Santillo in
Google Scholar
PubMed
Search for other papers by L Burrone in
Google Scholar
PubMed
Search for other papers by S Falvo in
Google Scholar
PubMed
Search for other papers by R Senese in
Google Scholar
PubMed
Search for other papers by A Lanni in
Google Scholar
PubMed
Search for other papers by G Chieffi Baccari in
Google Scholar
PubMed
peroxisomal fatty acid oxidation respectively. Next, because T 3 stimulates fat oxidation by acting at the mitochondrial and peroxisomal levels, we studied the effect of an animal's thyroid state on the mitochondria, correlating mitochondrial activity and
Search for other papers by Taija Saloniemi in
Google Scholar
PubMed
Search for other papers by Heli Jokela in
Google Scholar
PubMed
Department of Physiology, Turku Center for Disease Modeling, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, FI-20014 Turku, Finland
Search for other papers by Leena Strauss in
Google Scholar
PubMed
Department of Physiology, Turku Center for Disease Modeling, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, FI-20014 Turku, Finland
Search for other papers by Pirjo Pakarinen in
Google Scholar
PubMed
Department of Physiology, Turku Center for Disease Modeling, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, FI-20014 Turku, Finland
Search for other papers by Matti Poutanen in
Google Scholar
PubMed
characterised inborn errors of cholesterol synthesis are indicated in red. HSD17B12 The mammalian HSD17B12 was initially characterised as a 3-ketoacyl-CoA reductase, involved in the long-chain fatty acid synthesis ( Moon & Horton 2003 ). Both the human and the
Faculty of Chemical Technology, University of Chemistry and Technology Prague, Prague, Czech Republic
Search for other papers by Martina Bugáňová in
Google Scholar
PubMed
Search for other papers by Helena Pelantová in
Google Scholar
PubMed
Search for other papers by Martina Holubová in
Google Scholar
PubMed
Search for other papers by Blanka Šedivá in
Google Scholar
PubMed
Search for other papers by Lenka Maletínská in
Google Scholar
PubMed
Search for other papers by Blanka Železná in
Google Scholar
PubMed
Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic
Search for other papers by Jaroslav Kuneš in
Google Scholar
PubMed
Faculty of Chemical Technology, University of Chemistry and Technology Prague, Prague, Czech Republic
Search for other papers by Petr Kačer in
Google Scholar
PubMed
Search for other papers by Marek Kuzma in
Google Scholar
PubMed
Institute of Medical Biochemistry and Laboratory Diagnostics, 1st Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
Search for other papers by Martin Haluzík in
Google Scholar
PubMed
Clinical Endocrinology and Metabolism 96 2027 – 2031 . ( doi:10.1210/jc.2011-0599 ) Fabbrini E Sullivan S Klein S 2010 Obesity and nonalcoholic fatty liver disease: biochemical, metabolic, and clinical implications . Hepatology 51
Search for other papers by Chunxia Yu in
Google Scholar
PubMed
Search for other papers by Sujuan Liu in
Google Scholar
PubMed
Search for other papers by Liqin Chen in
Google Scholar
PubMed
Search for other papers by Jun Shen in
Google Scholar
PubMed
Search for other papers by Yanmei Niu in
Google Scholar
PubMed
Search for other papers by Tianyi Wang in
Google Scholar
PubMed
Search for other papers by Wanqi Zhang in
Google Scholar
PubMed
Department of Rehabilitation, School of Medical Technology, Tianjin Medical University, Tianjin, China
Search for other papers by Li Fu in
Google Scholar
PubMed
Jiancheng, China, A111-1) and total cholesterol assay kit (Nanjing Jiancheng, China, A110-1), respectively. Measurement of plasma free fatty acids (FFAs) and insulin concentrations were performed using FFA ELISA kit (EL701771-96T) and an insulin ELISA kit