Lipolysis metabolism

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Organisms

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Organisms

Mus musculus (54)
Homo sapiens (31)
Drosophila melanogaster (4)
Rattus norvegicus (3)
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Caenorhabditis elegans (2)
Penicillium roqueforti (1)
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Repository

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Cell culture (6)
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Disease

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Technology Type

Mass Spectrometry (32)
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Instrument Platform

Liquid Chromatography MS - negative - reverse phase (8)
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Gas Chromatography MS - positive (6)
Q Exactive (3)
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Liquid Chromatography MS - negative - hilic (3)
The Agilent scanner G2565BA (2)
Agilent�s Microarray Hybridization Oven (2)
NanoDrop ND-1000 Spectrophotometer (NanoDrop Technologies) (2)
Q Exactive HF (2)
Liquid Chromatography MS - positive (2)
Liquid Chromatography MS - negative - reverse-phase (2)
Liquid Chromatography MS - positive - hilic (2)
Illumina HiSeq 2500 (1)
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Liquid Chromatography MS - alternating - hilic (1)
Liquid Chromatography MS - positive - reverse-phase (1)

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CHEBI ID

CHEBI:17351 (4)
CHEBI:30915 (3)
CHEBI:48131 (3)
CHEBI:15891 (3)
CHEBI:16196 (3)
CHEBI:30805 (3)
CHEBI:9907 (2)
CHEBI:30830 (2)
CHEBI:45571 (2)
CHEBI:69081 (2)
CHEBI:17553 (2)
CHEBI:78697 (2)
CHEBI:6650 (2)
CHEBI:27266 (2)
CHEBI:25017 (2)
CHEBI:24898 (2)
CHEBI:26271 (2)
CHEBI:16449 (2)
CHEBI:25094 (2)
CHEBI:26986 (2)
CHEBI:22660 (2)
CHEBI:18186 (2)
CHEBI:17822 (2)
CHEBI:131691 (2)
CHEBI:72741 (2)
CHEBI:32389 (2)
CHEBI:30772 (2)
CHEBI:29019 (2)
CHEBI:17515 (2)
CHEBI:17418 (2)

Metabolite Name

LysoPE(0:0/20:0) (2)
Gamma-Glutamylcysteine (2)
Sphingosine (2)
LysoPE(0:0/20:4(5Z,8Z,11Z,14Z)) (2)
Taurine (2)
Adrenic acid (2)
L-Tyrosine (2)
Malic acid (2)
Adenosine (2)
Oleic acid (2)
Adenine (2)
Linoleic acid (2)
Palmitoleic acid (2)
Myristic acid (2)
Uric acid (2)
LPC(18:0)+HCOO (1)
LPC(17:1)+HCOO (1)
LPC(17:0)+HCOO (1)
LPC(16:1e)+HCOO (1)
LPC(16:1)+HCOO (1)
LPC(16:0)+HCOO (1)
LPC(14:1e)+HCOO (1)
LPC(14:0)+HCOO (1)
Hex3Cer(d27:0)-H (1)
Hex2Cer(m44:0+O)+HCOO (1)
Hex2Cer(m40:4)-H (1)
Hex2Cer(m40:2)-H (1)
Hex2Cer(m38:2)-H (1)
Hex2Cer(m38:0+O)+HCOO (1)
Hex2Cer(m35:1)-H (1)

First Public Date

2025 (19)
2026 (18)
2022 (16)
2024 (15)
2023 (10)
2014 (10)
2020 (9)
2021 (8)
2019 (7)
2015 (5)
2018 (1)
2017 (1)

Study type

Transcription profiling by array (40)
RNA-seq of coding RNA (4)
Transcription profiling by SAGE (1)
Other (1)
Methylation profiling by array (1)

Release Date

2022 (153)
2023 (135)
2021 (127)
2024 (119)
2025 (117)
2020 (116)
2019 (89)
2018 (80)
2016 (70)
2017 (60)
2015 (57)
2014 (41)
2026 (28)
2011 (25)
2013 (23)
2012 (22)
2010 (20)
2009 (12)
2008 (5)
2007 (4)
2006 (4)
2004 (1)
2005 (1)
2003 (1)
2001 (1)

Lab affiliation

Shanghai Diabetes Institute, Department of Endocrinology and Metabolism, Shanghai Sixth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine (1)
Institute of Metabolic Science, University of Cambridge, UK (1)
Lipolysis and Bacterial Pathogenicity team, LISM UMR7255, CNRS, Aix-Marseille Univ. , IMM FR3479, Marseille, France (1)
Charles Perkins Centre and School of Medical Sciences, University of Sydney, Australia (1)
Proteomics and Metabolomics Unit Experimental Neuroscience Department IRCCS-S.Lucia Foundation Roma, Italy (1)
School of Life and Environmental Sciences, Faculty of Science, University of Sydney. (1)
Singapore Professor of Biological Engineering Professor of Biological Engineering Massachusetts Institute of Technology Department of Biological Engineering, 56-731 77 Massachusetts Ave. Cambridge, MA 02139 (1)
Proteome Centre Tuebingen (1)
Faculty of Technical Chemistry, Institute of Chemical Technologies and Analytics, Technische Universität Wien, Getreidemarkt 9/164, 1060 Vienna, Austria (1)
Stéphane Canaan, Ph. D , Group Leader, "Lipolysis and Bacterial Pathogenicity" Laboratory of Engineering of Macromolecular Systems UMR7255-CNRS, 31 Chemin Joseph-Aiguier 13402 MARSEILLE cedex 20 (1)
Department of Functional and Molecular Biology, Institute of Biology, State University of Campinas (UNICAMP), Brazil (1)
Laboratory of Metabolism of Bioactive Lipids, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic (1)
Dr. rer. nat. Birgit Knebel Institute for Clinical Biochemistry and Pathobiochemistry German Diabetes Center (DDZ) Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf Auf´m Hennekamp 65 40225 Düsseldorf, Germany Tel.: +49-(0)-211-33-82-536 birgit.knebel@ddz.de www.ddz.de (1)
Institute for Diabetes and Obesity, Helmholtz Zentrum München, Neuherberg, Germany. and German Center for Diabetes Research (DZD), Neuherberg, Germany;d German Center for Diabetes Research, Neuherberg, Germany (1)
Program in Molecular Medicine, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA (1)
Boston University School of Medicine (1)
Department of Physiology, The University of Melbourne, Melbourne, Victoria, 3010 Australia (1)
Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences (1)
Hunan Institute of Animal and Veterinary Science (1)
Shenzhen University (1)
Sun Yat-sen University (1)
Lipolysis and bacterial Pathogenicity Team LISM UMR7255 CNRS 31, chemin Joseph Aiguier - CS 70071 F-13402 marseille cedex 09 (1)
University of Potsdam, Institute of Nutritional Science, Molecular and Experimental Nutritional Medicine, Nuthetal, Germany (1)
Xiangya Hospital of Central South University. (1)
Institut für Pharmazeutische Wissenschaften, Universitry of Graz, Austria (1)
Department of Biochemistry and Molecular Biology, University of Southern Denmark (1)
Department of Pharmacology, University of São Paulo. São Paulo, SP, Brazil. (1)
Cambridge Institute for Medical Research, University of Cambridge, Hills Road, Cambridge, CB2 0XY, UK (1)
Instituto de Investigaciones Sanitarias de Santiago de Compostela (1)
Charles Perkins Centre, The University of Sydney (1)

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ER stress inhibits liver fatty acid oxidation while unmitigated stress leads to anorexia-induced lipolysis and both liver and kidney steatosis

The unfolded protein response (UPR), induced by endoplasmic reticulum (ER) stress, regulates the expression of factors that restore protein folding homeostasis. However, in the liver and kidney, ER stress also leads to lipid accumulation, accompanied at least in the liver by transcriptional suppress...

2017-06-23 | MTBLS472 | MetaboLights

Calorie restriction-like effects of 30 days of resveratrol supplementation on energy metabolism and metabolic profile in obese humans

Resveratrol is a naturally occurring compound that profoundly affects energy metabolism and mitochondrial function and serves as a calorie restriction mimetic, at least in animal models of obesity. Here we treated 10 healthy, obese men with placebo and 150 mg/day resveratrol in a randomized double-b...

ORGANISM(S): Homo sapiens

2011-11-08 | E-GEOD-32357 | biostudies-arrayexpress

ANKRD53 is downregulated in human obesity and coordinates lipolysis with mitochondrial oxidative metabolism in adipocytes.

Not available

S-EPMC12924745 | biostudies-literature

Next-generation sequencing for the fat mass and obesity-associated protein (FTO) binding mRNA

Purpose: The goals of this study are to investigate the mRNAs that bind to the FTO protein in the white fat tissue from mice. Methods: 1. White fat from CAG promoter driven transgenic Flag-tagged FTO mice were extracted with RNA protected. 2. Flag-FTO proteins were immunoprecipitated with control I...

ORGANISM(S): Mus musculus

2016-01-05 | E-GEOD-74255 | biostudies-arrayexpress

Lipolysis regulates major transcriptional programs in brown adipocytes

PRJNA837456 | ENA

Lipolysis regulates major transcriptional programs in brown adipocytes [hBA]

PRJNA839248 | ENA

Adipose tissue lipolysis is regulated by PAQR11 via altering protein stability of phosphodiesterase 4D.

Not available

S-EPMC7906896 | biostudies-literature

Lipolysis regulates major transcriptional programs in brown adipocytes [DOX exp]

PRJNA843958 | ENA

GDF15 links adipose tissue lipolysis with anxiety.