Abstract:Human brown adipose tissue (BAT) can be activated to increase glucose uptake and energy expenditure, making it a potential target for treating obesity and metabolic disease. Data on the functional and anatomic characteristics of BAT are limited, however. In 20 healthy young men [12 lean, mean body mass index (BMI) 23.2 ± 1.9 kg/m 2 ; 8 obese, BMI 34.8 ± 3.3 kg/m 2 ] after 5 h of tolerable cold exposure, we measured BAT volume and activity by 18 F-labeled fluorodeoxyglucose positron emission tomography/computer… Show more
“…Although the relative volume of BAT in humans may be limited compared with skeletal muscle, the uptake of fatty acids per gram tissue by BAT exceeds that by skeletal muscle by >10-fold (figure 3F). Also, a recent paper redefined whole-body BAT distribution in humans and concluded that its metabolic capacity is substantially higher than usually reported 40. The effects of butyrate on fatty acid uptake and oxidation by BAT we observe in mice may thus well be relevant for humans.…”
“…Although the relative volume of BAT in humans may be limited compared with skeletal muscle, the uptake of fatty acids per gram tissue by BAT exceeds that by skeletal muscle by >10-fold (figure 3F). Also, a recent paper redefined whole-body BAT distribution in humans and concluded that its metabolic capacity is substantially higher than usually reported 40. The effects of butyrate on fatty acid uptake and oxidation by BAT we observe in mice may thus well be relevant for humans.…”
“…It has been reported that higher human in vivo BAT activity changes metabolism through increased energy expenditure . However, the current topic of debate questions whether we fully grasp the complete thermogenic potential of active human BAT . The finding that ZIC1 was positively associated with age and BMI and negatively associated with BAT activity is interesting because, to the best of our knowledge, no links have been established between BAT activity and ZIC1.…”
Objective: Human brown adipose tissue (BAT) activity decreases with age and obesity. In addition to uncoupling protein 1 (UCP1), several genetic markers of BAT in humans have been published. However, the link between human BAT activity and genetic markers has been inadequately explored. Methods: White adipose tissue (WAT) and BAT biopsies were obtained from 16 patients undergoing deep neck surgery. In vitro differentiated adipocytes were used to measure norepinephrine-stimulated mitochondrial uncoupling as a measure of in vitro BAT activity. Gene expression was determined in adipose tissue biopsies. Results: Norepinephrine increased in vitro BAT activity in adipocytes derived from human BAT, and this increase was abolished by propranolol. Furthermore, in vitro BAT activity showed a negative correlation to age and BMI. UCP1 messenger RNA (mRNA) expression showed a positive correlation to in vitro BAT activity, while zinc finger protein of cerebellum 1 (ZIC1) mRNA showed a negative correlation to in vitro BAT activity. In human BAT biopsies, UCP1 mRNA showed negative correlations to age and BMI, while ZIC1 mRNA showed positive correlations to age and BMI. Conclusions: Differentiated adipocytes derived from human BAT maintain intrinsic characteristics of the donor. High ZIC1 mRNA does not necessarily reflect high BAT activity.
“…Another limitation of the current study is that not all fat is in adipose tissue, and we were unable to adjust our organ mass estimates for nonadipose intracellular triglyceride content . Similarly, we did not build brown fat, a potential source of thermogenesis, into our models . Lastly, we contrasted obesity‐tissue features in men to those observed in our sample of women.…”
Objective
Chronic positive energy balance leads to obesity, and the “excess” weight is usually described as consisting solely of adipose tissue (AT) or its two components, fat and fat‐free mass (nonfat cell mass, extracellular fluid). This study aimed to clarify the nature of “obesity” tissue.
Methods
A total of 333 adults had AT, skin, skeletal muscle, bone, heart, liver, kidney, spleen, brain, and residual mass measured or derived using magnetic resonance imaging and dual‐energy x‐ray absorptiometry. First, associations between these components and AT were examined by developing multiple regression models. Next, obesity‐tissue composition was developed by deriving mean component mass differences between participant groups with normal weight (BMI < 25 kg/m2) and those with obesity (BMI > 29.9 kg/m2); respective resting energy expenditures and metabolizable energy and protein contents were calculated.
Results
AT significantly predicted organ‐tissue mass in 17 of 18 multiple regression models. In addition to AT and skeletal muscle, the following associations were found: skin, liver, and bone were main contributors to obesity‐tissue composition; liver, kidneys, and heart to resting energy expenditure; and skin, liver, and bone to metabolizable energy and protein contents. A pronounced sexual dimorphism was present in all three models.
Conclusions
Obesity is characterized not only by excess AT but by increases in the masses of other “companion” organs and tissues and their related metabolic properties.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.