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Beta2‑adrenergic stimulation increases energy expenditure at rest, but not during submaximal exercise in active overweight men

Citation

Onslev, J and Jacobson, G and Narkowicz, C and Backer, V and Kalsen, A and Kreiberg, M and Jessen, S and Bangsbo, J and Hostrup, M, Beta2‑adrenergic stimulation increases energy expenditure at rest, but not during submaximal exercise in active overweight men, European Journal of Applied Physiology pp. 1-9. ISSN 1439-6319 (2017) [Refereed Article]

Copyright Statement

Copyright 2017 Springer-Verlag GmbH Germany

DOI: doi:10.1007/s00421-017-3679-9

Abstract

Purpose: β2-Agonists have been proposed as weight-loss treatment, because they elevate energy expenditure. However, it is unknown what effect β2-agonists have on energy expenditure in overweight individuals. Furthermore, the influence of β2-agonist R- and S-enantiomer ratio for the increased energy expenditure is insufficiently explored.

Methods: Nineteen males were included in the study of which 14 completed. Subjects were 31.6 (±3.5) years [mean (±95% CI)] and had a fat percentage of 22.7 (±2.1)%. On separate days, subjects received either placebo or inhaled racemic (rac-) formoterol (2 × 27 µg). After an overnight fast, energy expenditure and substrate oxidation were estimated by indirect calorimetry at rest and during submaximal exercise. Plasma (R,R)- and (S,S)-formoterol enantiomer levels were measured by ultra-performance liquid chromatograph–mass spectrometry.

Results: At rest, energy expenditure and fat oxidation were 12% (P ≤ 0.001) and 38% (P = 0.006) higher for rac-formoterol than placebo. Systemic (R,R):(S,S) formoterol ratio was correlated with change in energy expenditure at rest in response to rac-formoterol (r = 0.63, P = 0.028), whereas no association was observed between fat percentage and rac-formoterol-induced change in energy expenditure. During exercise, energy expenditure was not different between treatments, although carbohydrate oxidation was 15% higher (P = 0.021) for rac-formoterol than placebo. Rac-formoterol-induced shift in substrate choice from rest to exercise was related to plasma ln-rac-formoterol concentrations (r = 0.75, P = 0.005).

Conclusion: Selective β2-adrenoceptor agonism effectively increases metabolic rate and fat oxidation in overweight individuals. The potential for weight loss induced by β2-agonists may be greater for R-enantiopure formulations.

Item Details

Item Type:Refereed Article
Keywords:beta2-agonist energy expenditure obesity
Research Division:Medical and Health Sciences
Research Group:Pharmacology and Pharmaceutical Sciences
Research Field:Clinical Pharmacology and Therapeutics
Objective Division:Health
Objective Group:Clinical Health (Organs, Diseases and Abnormal Conditions)
Objective Field:Clinical Health (Organs, Diseases and Abnormal Conditions) not elsewhere classified
Author:Jacobson, G (Dr Glenn Jacobson)
Author:Narkowicz, C (Dr Christian Narkowicz)
ID Code:118572
Year Published:2017
Web of Science® Times Cited:1
Deposited By:Pharmacy
Deposited On:2017-07-13
Last Modified:2017-09-29
Downloads:0

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