Seasonal variations in the mass and composition of brown adipose tissue in the meadow vole, Microtus pennsylvanicus

1969 ◽  
Vol 47 (4) ◽  
pp. 547-555 ◽  
Author(s):  
L. A. Didow ◽  
J. S. Hayward

Wild meadow voles were collected each month of the year and analyzed for the mass and composition of their brown adipose tissue. The relative mass of brown adipose tissue decreased with increasing body weight in both summer and winter.Seasonal changes in the relative mass of brown adipose tissue were inversely related to seasonal changes in ambient temperature. In mature voles, the relative mass of brown adipose tissue was lowest during summer (0.5%) and increased rapidly to a level of 1.7% in early winter. Similarly, immature voles had their lowest relative mass in summer (1.0%) and increased this to 2.3% in winter. Both groups showed some decrease in the winter amount of the tissue when the subnivean environment became established. The percentage composition of brown adipose tissue with respect to water, lipid, and protein did not change significantly through the year.The results provide corroboration for laboratory studies which show that the mass and composition of brown adipose tissue are related to the requirement for cold thermogenesis. In voles, this requirement was present throughout the year and varied only in degree.

1984 ◽  
Vol 62 (7) ◽  
pp. 623-630 ◽  
Author(s):  
Ludwik J. Bukowiecki

The sequence of metabolic events leading to increased calorigenesis in brown adipose tissue has been reviewed. The first step of this sequence consists in the binding of norepinephrine to adrenergic receptors of the beta1 subtype. This results in the stimulation of adenylate cyclase and activation of lipolysis via the system of protein kinases. Hormone-sensitive lipases represent the "flux-generating" step regulating mitochondrial respiration. Fatty acids released from intracellular triglyceride droplets in consequence of lipase activation play a messenger role between lipolysis and mitochondrial respiration. They stimulate respiration by serving as substrates for beta oxidation (via carnitine-dependent pathways) and (or) by simultaneously increasing mitochondrial permeability to protons (physiological "loose coupling"). The control of brown adipose tissue respiration by lipolysis represents a self-regulatory process, as excessive concentrations of fatty acids retroinhibit lipolysis. At the mitochondrial level, fatty acids appear to interact with an "uncoupling" protein (thermogenin or 32 000 relative mass protein) localized in the inner membrane that confers upon brown adipose mitochondria a unique sensitivity for fatty acid uncoupling. This explains that, contrary to other tissues, respiration is principally controlled in brown adipose tissue by substrate supply (mainly long-chain fatty acids), rather than by the phosphorylation state ratio.


1982 ◽  
Vol 30 (1) ◽  
pp. 15 ◽  
Author(s):  
CR Tidemann

Information on seasonal changes in activity, body weight and brown adipose tissue weight was collected from a wild population of a small Australian vespertilionid, Eptesicus vulturnus. Both sexes, but especially females, became less active during the colder months of the year. Males maintained body weight and brown adipose tissue weight during winter, as do non-hibernating mammals. Females lost brown adipose tissue and body weight during winter, as do hibernators. The relationship between the sex differences in overwintering behaviour and the reproductive cycle is discussed.


2018 ◽  
Vol 50 (1) ◽  
pp. 52-66 ◽  
Author(s):  
Michal Pravenec ◽  
Laura M. Saba ◽  
Václav Zídek ◽  
Vladimír Landa ◽  
Petr Mlejnek ◽  
...  

Brown adipose tissue (BAT) has been suggested to play an important role in lipid and glucose metabolism in rodents and possibly also in humans. In the current study, we used genetic and correlation analyses in the BXH/HXB recombinant inbred (RI) strains, derived from Brown Norway (BN) and spontaneously hypertensive rats (SHR), to identify genetic determinants of BAT function. Linkage analyses revealed a quantitative trait locus (QTL) associated with interscapular BAT mass on chromosome 4 and two closely linked QTLs associated with glucose oxidation and glucose incorporation into BAT lipids on chromosome 2. Using weighted gene coexpression network analysis (WGCNA) we identified 1,147 gene coexpression modules in the BAT from BXH/HXB rats and mapped their module eigengene QTLs. Through an unsupervised analysis, we identified modules related to BAT relative mass and function. The Coral4.1 coexpression module is associated with BAT relative mass (includes Cd36 highly connected gene), and the Darkseagreen coexpression module is associated with glucose incorporation into BAT lipids (includes Hiat1, Fmo5, and Sort1 highly connected transcripts). Because multiple statistical criteria were used to identify candidate modules, significance thresholds for individual tests were not adjusted for multiple comparisons across modules. In summary, a systems genetic analysis using genomic and quantitative transcriptomic and physiological information has produced confirmation of several known genetic factors and significant insight into novel genetic components functioning in BAT and possibly contributing to traits characteristic of the metabolic syndrome.


2020 ◽  
Vol 477 (7) ◽  
pp. 1261-1286 ◽  
Author(s):  
Marie Anne Richard ◽  
Hannah Pallubinsky ◽  
Denis P. Blondin

Brown adipose tissue (BAT) has long been described according to its histological features as a multilocular, lipid-containing tissue, light brown in color, that is also responsive to the cold and found especially in hibernating mammals and human infants. Its presence in both hibernators and human infants, combined with its function as a heat-generating organ, raised many questions about its role in humans. Early characterizations of the tissue in humans focused on its progressive atrophy with age and its apparent importance for cold-exposed workers. However, the use of positron emission tomography (PET) with the glucose tracer [18F]fluorodeoxyglucose ([18F]FDG) made it possible to begin characterizing the possible function of BAT in adult humans, and whether it could play a role in the prevention or treatment of obesity and type 2 diabetes (T2D). This review focuses on the in vivo functional characterization of human BAT, the methodological approaches applied to examine these features and addresses critical gaps that remain in moving the field forward. Specifically, we describe the anatomical and biomolecular features of human BAT, the modalities and applications of non-invasive tools such as PET and magnetic resonance imaging coupled with spectroscopy (MRI/MRS) to study BAT morphology and function in vivo, and finally describe the functional characteristics of human BAT that have only been possible through the development and application of such tools.


2011 ◽  
Vol 6 (S 01) ◽  
Author(s):  
M Merkel ◽  
A Bartelt ◽  
K Brügelmann ◽  
J Heeren

2014 ◽  
Vol 9 (S 01) ◽  
Author(s):  
K Krause ◽  
M Kranz ◽  
V Zeisig ◽  
N Klöting ◽  
K Steinhoff ◽  
...  

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