Activation of human brown adipose tissue by a β3-adrenergic receptor agonist

Aaron M Cypess, Lauren S Weiner, Carla Roberts-Toler, Elisa Franquet Elía, Skyler H Kessler, Peter A Kahn, Jeffrey English, Kelly Chatman, Sunia A Trauger, Alessandro Doria, Gerald M Kolodny, Aaron M Cypess, Lauren S Weiner, Carla Roberts-Toler, Elisa Franquet Elía, Skyler H Kessler, Peter A Kahn, Jeffrey English, Kelly Chatman, Sunia A Trauger, Alessandro Doria, Gerald M Kolodny

Abstract

Increasing energy expenditure through activation of endogenous brown adipose tissue (BAT) is a potential approach to treat obesity and diabetes. The class of β3-adrenergic receptor (AR) agonists stimulates rodent BAT, but this activity has never been demonstrated in humans. Here we determined the ability of 200 mg oral mirabegron (Myrbetriq, Astellas Pharma, Inc.), a β3-AR agonist currently approved to treat overactive bladder, to stimulate BAT as compared to placebo. Mirabegron led to higher BAT metabolic activity as measured via (18)F-fluorodeoxyglucose ((18)F-FDG) using positron emission tomography (PET) combined with computed tomography (CT) in all twelve healthy male subjects (p = 0.001), and it increased resting metabolic rate (RMR) by 203 ± 40 kcal/day (+13%; p = 0.001). BAT metabolic activity was also a significant predictor of the changes in RMR (p = 0.006). Therefore, a β3-AR agonist can stimulate human BAT thermogenesis and may be a promising treatment for metabolic disease.

Copyright © 2015 Elsevier Inc. All rights reserved.

Figures

Figure 1. Metabolic Effects of the β3-AR…
Figure 1. Metabolic Effects of the β3-AR Agonist Mirabegron
(A) PET images of a 21-year-old man who was given placebo (left) or 200 mg of the β3-AR agonist mirabegron (right). Twelve male subjects were given placebo or 200 mg mirabegron. (B) BAT metabolic activity as reflected by 18F-FDG uptake. (C) Resting metabolic rate. (D) Heart rate. (E) Systolic BP. (F) Diastolic BP. Each circle represents a single subject, and the numbers correspond to subject identification number in Figure S2. The dashes represent the mean. See also Figure S2.
Figure 2. Tissue Glucose Uptake
Figure 2. Tissue Glucose Uptake
18F-FDG uptake in the twelve volunteers when given placebo or 200 mg mirabegron is shown for different tissues. Each circle represents a single subject. (A) Myocardium. (B) Subcutaneous WAT. (C) Skeletal muscle. (D) Liver. See also Table S1.
Figure 3. Predictors of Resting Metabolic Rate
Figure 3. Predictors of Resting Metabolic Rate
(A) Placebo-induced BAT activity. (B) Two-hundred milligram mirabegron-induced BAT activity. (C) Body fat mass with placebo. (D) Body fat mass with 200 mg mirabegron. See also Figure S3.

Source: PubMed

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