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Michael E Symonds Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, University of Nottingham, Nottingham, UK
Nottingham Digestive Disease Centre and Biomedical Research Centre, School of Medicine, University of Nottingham, Nottingham, UK

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Mark Pope Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, University of Nottingham, Nottingham, UK

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Ian Bloor Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, University of Nottingham, Nottingham, UK

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James Law Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, University of Nottingham, Nottingham, UK

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Reham Alagal Department of Physical Sport Science, Princess Nourah Bint AbdulRahman University, Riyadh, Saudi Arabia

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Helen Budge Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, University of Nottingham, Nottingham, UK

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(UCP)1 located on the inner mitochondrial membrane, with beige fat possessing ~10-fold less UCP1 than classic brown adipocytes ( Cannon & Nedergaard 2011 ). When UCP1 is activated it enables the free flow of protons across the mitochondria without the

Article Type:
Review Article
DOI:
https://doi.org/10.1530/JOE-20-0075
Volume/Issue:
Volume 248: Issue 1
Free access
Guillermo Vazquez-Anaya Department of Molecular & Cellular Biology, University of California, Merced, California, USA

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Bridget Martinez Department of Molecular & Cellular Biology, University of California, Merced, California, USA

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José G Soñanez-Organis Division of Science and Engineering, Department of Chemical Biological and Agropecuary Sciences, University of Sonora, Navojoa, Sonora, Mexico

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Daisuke Nakano Department of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan

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Akira Nishiyama Department of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, Japan

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Rudy M Ortiz Department of Molecular & Cellular Biology, University of California, Merced, California, USA

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relationship between TH and glucose homeostasis during insulin resistance conditions exist. Furthermore, the simultaneous contributions of exogenous T 4 on UCP2 and SIRT1 to improved glucose tolerance are not well defined. To address the effects of TH on

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-16-0428
Volume/Issue:
Volume 232: Issue 3
Free access
Caitlin S Wyrwoll School of Anatomy and Human Biology, School of Medicine and Pharmacology, The University of Western Australia, 35 Stirling Hwy, Crawley, Perth, Western Australia 6009, Australia

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Peter J Mark School of Anatomy and Human Biology, School of Medicine and Pharmacology, The University of Western Australia, 35 Stirling Hwy, Crawley, Perth, Western Australia 6009, Australia

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Trevor A Mori School of Anatomy and Human Biology, School of Medicine and Pharmacology, The University of Western Australia, 35 Stirling Hwy, Crawley, Perth, Western Australia 6009, Australia

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Brendan J Waddell School of Anatomy and Human Biology, School of Medicine and Pharmacology, The University of Western Australia, 35 Stirling Hwy, Crawley, Perth, Western Australia 6009, Australia

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-γ coactivator-1α (PPARGC1A), and uncoupling protein 3 ( UCP3 ) mRNAs, were also determined. These genes were targeted because PPARD is a key regulator of fuel metabolism ( Brunmair et al . 2006 ), the effects of which involve coactivation by PPARGC1A ( Finck

Article Type:
Research Article
DOI:
https://doi.org/10.1677/JOE-08-0210
Volume/Issue:
Volume 198: Issue 3
Free access
Vivian Cristine Calegari
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Claudio Cesar Zoppi
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Luiz Fernando Rezende
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Leonardo Reis Silveira Endocrine Pancreas and Metabolism Laboratory, Department of Biochemistry and Immunology, Department of Anatomy, Cellular Biology and Physiology and Biophysics, Institute of Biology, State University of Campinas (UNICAMP), PO Box 6109, Campinas, SP, CEP: 13083-865, Brazil

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Everardo Magalhães Carneiro
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Antonio Carlos Boschero
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were from analytical grade. Antibodies against GLUT2 (sc-7580) and UCP2 (sc-6526) were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Antibodies against peroxisome proliferator-activated receptor-γ coactivator-1-α (PGC-1α) (#2178), AMPK

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-10-0450
Volume/Issue:
Volume 208: Issue 3
Free access
Cintia B Ueta Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil
Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Gustavo W Fernandes Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Luciane P Capelo Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Tatiane L Fonseca Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Flávia D'Angelo Maculan Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Cecilia H A Gouveia Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Patrícia C Brum Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Marcelo A Christoffolete Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Marcelo S Aoki Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Carmen L Lancellotti Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Brian Kim Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Antonio C Bianco Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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Miriam O Ribeiro Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil

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rapidly removed and processed for mitochondrial isolation. Uncoupling protein-1 (UCP1; Santa Cruz Biotechnology) was quantified after mitochondrial proteins were size-fractionated by 12% SDS–PAGE and identified by western blotting. Intraperitoneal glucose

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-12-0155
Volume/Issue:
Volume 214: Issue 3
Free access
Xiaofeng Ding Department of Biochemistry and Molecular Biology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA
Key Laboratory of Protein Chemistry and Development Biology of State Education Ministry of China, College of Life Science, Hunan Normal University, Changsha, Hunan, China

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Yan Luo Department of Biochemistry and Molecular Biology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA
Department of Metabolism and Endocrinology, Metabolic Syndrome Research Center, Key Laboratory of Diabetes Immunology, Ministry of Education, National Clinical Research Center for Metabolic Diseases, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China

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Xing Zhang Department of Biochemistry and Molecular Biology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA
Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA

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Handong Zheng Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA

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Xin Yang Department of Biochemistry and Molecular Biology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA

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Xuexian Yang Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA

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Meilian Liu Department of Biochemistry and Molecular Biology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA
Department of Metabolism and Endocrinology, Metabolic Syndrome Research Center, Key Laboratory of Diabetes Immunology, Ministry of Education, National Clinical Research Center for Metabolic Diseases, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China

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feeding and leptin deficiency-induced obesity. Moreover, IL-33 administration dramatically upregulated the frequency of ILC2s and eosinophils and expression levels of UCP1 and tyrosine hydroxylase (TH) in sWAT of HFD-fed mice. Consistently, blocking IL-33

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-16-0229
Volume/Issue:
Volume 231: Issue 1
Free access
Michael E Symonds Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, School of Medicine, University of Nottingham, Nottingham, UK
Nottingham Digestive Disease Centre and Biomedical Research Centre, School of Medicine, University of Nottingham, Nottingham, UK

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Peter Aldiss Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, School of Medicine, University of Nottingham, Nottingham, UK

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Neele Dellschaft Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, School of Medicine, University of Nottingham, Nottingham, UK

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James Law Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, School of Medicine, University of Nottingham, Nottingham, UK

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Hernan P Fainberg Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, School of Medicine, University of Nottingham, Nottingham, UK

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Mark Pope Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, School of Medicine, University of Nottingham, Nottingham, UK

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Harold Sacks VA Endocrinology and Diabetes Division, VA Greater Los Angeles Healthcare System, and Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, California, USA

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Helen Budge Early Life Research Unit, Division of Child Health, Obstetrics & Gynaecology, School of Medicine, University of Nottingham, Nottingham, UK

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protein (UCP)1 on the inner mitochondrial membrane ( Cannon & Nedergaard 2004 ). When stimulated, UCP1 enables the free flow of protons across the mitochondria, by-passing the usual production of ATP, which occurs in the mitochondria of all other organs

Article Type:
Review Article
DOI:
https://doi.org/10.1530/JOE-18-0084
Volume/Issue:
Volume 238: Issue 1
Free access
P C Lisboa Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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E de Oliveira Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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A C Manhães Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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A P Santos-Silva Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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C R Pinheiro Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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V Younes-Rapozo Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil
Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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L C Faustino Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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T M Ortiga-Carvalho Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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E G Moura Laboratory of Endocrine Physiology, Laboratory of Neurophysiology, Carlos Chagas Filho Biophysic Institute, Biology Institute, State University of Rio de Janeiro, Rio de Janeiro 20551‐030, Brazil

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tissues such as hypothalamus, pituitary, thyroid, liver, BAT, skeletal muscle, heart, and testis; mGPD activity and TRβ1 protein expression in liver; and uncoupling protein 1 (UCP1) expression in BAT. In addition, we also studied both TSH-releasing hormone

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-14-0473
Volume/Issue:
Volume 224: Issue 3
Free access
Edward T Wargent Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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Jacqueline F O'Dowd Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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Mohamed S Zaibi Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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Dan Gao Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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Chen Bing Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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Paul Trayhurn Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK
Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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Michael A Cawthorne Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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Jonathan R S Arch Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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Claire J Stocker Clore Laboratory, Obesity Biology Unit, University of Buckingham, Hunter Street, Buckingham MK18 1EG, UK

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uncoupling protein-1 (UCP1) in brown adipose tissue and increase core temperature, suggestive of increased energy expenditure ( Granneman et al . 2003 , Inokuma et al . 2006 , Russell & Tisdale 2010 a , 2011 , 2012 a ). β 3 -Adrenoceptor agonists have

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JOE-12-0402
Volume/Issue:
Volume 216: Issue 2
Free access
Camilla Alexanderson
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Elias Eriksson Department of Physiology, Department of Pharmacology, Wallenberg Laboratory, Institute of Neuroscience and Physiology, Sahlgrenska Academy, Göteborg University, Box 434, SE-405 30 Göteborg, Sweden

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Elisabet Stener-Victorin
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Malin Lönn Department of Physiology, Department of Pharmacology, Wallenberg Laboratory, Institute of Neuroscience and Physiology, Sahlgrenska Academy, Göteborg University, Box 434, SE-405 30 Göteborg, Sweden

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Agneta Holmäng
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Pparg Peroxisome proliferator-activated receptor γ Rn00440945_m1 NM_013124.1 Rbp4 Retinol binding protein 4 Rn01451318_m1 XM_215285.4 Tgfβ1 Transforming growth factor β-1 Rn00572010_m1 NM_021578.1 Ucp 2 Uncoupling protein 2 Rn00571166_m1 NM_019354.1 Ucp

Article Type:
Research Article
DOI:
https://doi.org/10.1677/JOE-08-0534
Volume/Issue:
Volume 201: Issue 1
Free access