Brown Adipose Tissue Exhibits a Glucose-Responsive Thermogenic Biorhythm in Humans

High abundance of brown adipose tissue (BAT) is linked to lower glycaemia in humans, leading to the belief that BAT may protect against diabetes. The relationship between BAT glucose utilization and systemic glucose homeostasis has not been defined. In this paper we have characterized glycaemic excu...

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Published inCell metabolism Vol. 23; no. 4; pp. 602 - 609
Main Authors Lee, Paul, Bova, Ron, Schofield, Lynne, Bryant, Wendy, Dieckmann, William, Slattery, Anthony, Govendir, Matt A., Emmett, Louise, Greenfield, Jerry R.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 12.04.2016
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Abstract High abundance of brown adipose tissue (BAT) is linked to lower glycaemia in humans, leading to the belief that BAT may protect against diabetes. The relationship between BAT glucose utilization and systemic glucose homeostasis has not been defined. In this paper we have characterized glycaemic excursions and BAT thermogenic responses in human brown adipocytes, BAT explants, and healthy adults through supraclavicular temperature profiling, revealing their circadian coupling in vivo and in vitro, orchestrated by UCP1, GLUT4, and Rev-erbα biorhythms. Extent of glycated haemoglobin also correlated positively with environmental temperature among community-dwelling patients. These data uncover potential crosstalk between BAT and glucose regulatory pathways, evident on cellular, tissue, individual, and population levels, and provide impetus to search for BAT harnessing strategies for therapeutic purposes. [Display omitted] •Brown fat utilizes glucose as substrate fuel to produce heat in humans•Human brown fat exhibits a thermogenic circadian rhythm•Brown fat circadian rhythm is glucose responsive•Low brown fat abundance is associated with greater glycaemic fluctuations Lee et al. reveal how glucose utilization by brown fat in humans is coupled with heat production in a circadian manner. Higher brown fat abundance correlates with lesser glycemia variability, suggesting that brown fat may help buffer glucose fluctuations and maintain whole-body glucose homeostasis over time.
AbstractList High abundance of brown adipose tissue (BAT) is linked to lower glycaemia in humans, leading to the belief that BAT may protect against diabetes. The relationship between BAT glucose utilization and systemic glucose homeostasis has not been defined. In this paper we have characterized glycaemic excursions and BAT thermogenic responses in human brown adipocytes, BAT explants, and healthy adults through supraclavicular temperature profiling, revealing their circadian coupling in vivo and in vitro, orchestrated by UCP1, GLUT4, and Rev-erbα biorhythms. Extent of glycated haemoglobin also correlated positively with environmental temperature among community-dwelling patients. These data uncover potential crosstalk between BAT and glucose regulatory pathways, evident on cellular, tissue, individual, and population levels, and provide impetus to search for BAT harnessing strategies for therapeutic purposes.
High abundance of brown adipose tissue (BAT) is linked to lower glycaemia in humans, leading to the belief that BAT may protect against diabetes. The relationship between BAT glucose utilization and systemic glucose homeostasis has not been defined. In this paper we have characterized glycaemic excursions and BAT thermogenic responses in human brown adipocytes, BAT explants, and healthy adults through supraclavicular temperature profiling, revealing their circadian coupling in vivo and in vitro, orchestrated by UCP1, GLUT4, and Rev-erbα biorhythms. Extent of glycated haemoglobin also correlated positively with environmental temperature among community-dwelling patients. These data uncover potential crosstalk between BAT and glucose regulatory pathways, evident on cellular, tissue, individual, and population levels, and provide impetus to search for BAT harnessing strategies for therapeutic purposes. [Display omitted] •Brown fat utilizes glucose as substrate fuel to produce heat in humans•Human brown fat exhibits a thermogenic circadian rhythm•Brown fat circadian rhythm is glucose responsive•Low brown fat abundance is associated with greater glycaemic fluctuations Lee et al. reveal how glucose utilization by brown fat in humans is coupled with heat production in a circadian manner. Higher brown fat abundance correlates with lesser glycemia variability, suggesting that brown fat may help buffer glucose fluctuations and maintain whole-body glucose homeostasis over time.
Author Lee, Paul
Bryant, Wendy
Govendir, Matt A.
Schofield, Lynne
Dieckmann, William
Greenfield, Jerry R.
Slattery, Anthony
Emmett, Louise
Bova, Ron
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  organization: Diabetes and Metabolism Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia
– sequence: 2
  givenname: Ron
  surname: Bova
  fullname: Bova, Ron
  organization: Department of Surgery, St. Vincent’s Hospital, Sydney, NSW 2010, Australia
– sequence: 3
  givenname: Lynne
  surname: Schofield
  fullname: Schofield, Lynne
  organization: Diabetes and Metabolism Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia
– sequence: 4
  givenname: Wendy
  surname: Bryant
  fullname: Bryant, Wendy
  organization: Diabetes Centre, St. Vincent’s Hospital, Sydney, NSW 2010, Australia
– sequence: 5
  givenname: William
  surname: Dieckmann
  fullname: Dieckmann, William
  organization: Department of Positron Emission Tomography, National Institutes of Health, Bethesda, MD 20892, USA
– sequence: 6
  givenname: Anthony
  surname: Slattery
  fullname: Slattery, Anthony
  organization: Department of PET and Nuclear Medicine, St. Vincent’s Hospital, Sydney, NSW 2010, Australia
– sequence: 7
  givenname: Matt A.
  surname: Govendir
  fullname: Govendir, Matt A.
  organization: Diabetes and Metabolism Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia
– sequence: 8
  givenname: Louise
  surname: Emmett
  fullname: Emmett, Louise
  organization: Department of PET and Nuclear Medicine, St. Vincent’s Hospital, Sydney, NSW 2010, Australia
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  givenname: Jerry R.
  surname: Greenfield
  fullname: Greenfield, Jerry R.
  organization: Diabetes and Metabolism Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26972823$$D View this record in MEDLINE/PubMed
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Keywords beige adipose
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Snippet High abundance of brown adipose tissue (BAT) is linked to lower glycaemia in humans, leading to the belief that BAT may protect against diabetes. The...
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SubjectTerms Adipocytes, Brown - metabolism
Adipose Tissue, Brown - physiology
Adult
beige adipose
Cells, Cultured
circadian
Circadian Rhythm
Female
Glucose - metabolism
Glucose Transporter Type 4 - metabolism
GLUT4
Humans
Male
Middle Aged
Nuclear Receptor Subfamily 1, Group D, Member 1 - metabolism
Rev-erb
Thermogenesis
UCP1
Uncoupling Protein 1 - metabolism
Young Adult
Title Brown Adipose Tissue Exhibits a Glucose-Responsive Thermogenic Biorhythm in Humans
URI https://dx.doi.org/10.1016/j.cmet.2016.02.007
https://www.ncbi.nlm.nih.gov/pubmed/26972823
https://search.proquest.com/docview/1781541465
Volume 23
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