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intracellular third messenger for DA, in BAT of pigs suggests a direct role of DA in brown adipocytes ( Meister et al . 1988 ). DA receptors appear to be present in BAT homogenates obtained from rats, as suggested by the response of AC to various DA receptor
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are specialized in energy preservation in the form of triglycerides. However, adipose tissue also contains another type of fat cells called ‘brown adipocyte’. By contrast to white adipose tissue (WAT), brown adipose tissue (BAT) plays an active role in
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rats. Moreover, we have recently shown that brown adipocytes are also endocrine cells able to secrete leptin ( Buyse et al. 2001 ) and other adipocytokines such as resistin and adiponectin, two adipocyte-specific secretory factors involved in glucose
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specific marker of BAT. In floating brown adipocytes, D2 is stimulated by adrenergic agents ( Obregón et al. 1987 ), and synergism between the α1 and β adrenergic pathways has been described ( Raasmaja & Larsen 1989 ). In addition, BAT D2
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands
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Institute for Cardiovascular Prevention (IPEK), Ludwig Maximilian’s University, Munich, Germany
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Institute for Cardiovascular Prevention (IPEK), Ludwig Maximilian’s University, Munich, Germany
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Introduction Brown adipose tissue (BAT) contributes to the control of body temperature by the production of heat in response to cold. Brown adipocytes have numerous mitochondria that contain uncoupling protein 1 (UCP1). Activation of brown
Wellcome Trust Sanger Institute, Metabolic Research Laboratories, Wellcome Trust Genome Campus, Hinxton, UK
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Wellcome Trust Sanger Institute, Metabolic Research Laboratories, Wellcome Trust Genome Campus, Hinxton, UK
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method of obtaining human brown adipocytes from human BAT is through biopsies, which tend to be both small and surgically difficult to obtain, giving access to a very limited numbers of cells. This limits the possibilities for investigating human BAT
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Shanghai Clinical Center for Endocrine and Metabolic Diseases, Laboratory for Endocrine and Metabolism, Shanghai Institute of Endocrine and Metabolic Diseases, Department of Endocrinology and Metabolism, Shanghai Key Laboratory for Endocrine Tumors and E-Institutes of Shanghai Universities, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin 2nd Road, Shanghai 200025, China
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metabolic dysfunction, Ehrlund et al . (2013) indicated that SFRP5 in the WAT of Caucasians is not influenced by obesity. In light of the profound but conflicting effects of SFRP5 on adipogenesis and its unknown effect on brown adipocyte differentiation
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photomicrographs ( Fig. 4A ) show brown adipocytes that resemble unilocular white adipocytes in the HF group, and the whitening phenomenon contrasts with the multilocular brown adipocytes in the C group. The HF group showed increased BAT mass/g BM (+33%, Table 2
Department of Physiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
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Department of Experimental Vascular Medicine, Amsterdam University Medical Centers, Location AMC, Amsterdam, the Netherlands
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). Treatment of cultured brown adipocytes with sex steroids confirmed that E2 facilitates while testosterone inhibits NE-induced lipolysis, an initial step of BAT thermogenesis ( Monjo et al. 2003 ). While sex steroids may control BAT thermogenic activity
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. Canonical regulation is via the SNS. Of particular interest is the fact that many of the recently characterised molecules signal through specific receptors to enhance the capacity of brown adipocytes to respond to adrenergic stimulation. The range of tissues