The effect of caffeine and albuterol on body composition and metabolic rate

The effect of caffeine and albuterol on body composition and metabolic rate / Ann G. Liu, Kenneth P. Arceneaux III, Jessica T. Chu, Gregory Jacob Jr., Allyson L. Schreiber, Russell C. Tipton, Ying Yu, William D. Johnson, Frank L. Greenway, Stefany D. Primeaux. - (Obesity 23 (2015) 9 (September); p. 1830-1835).
- PMID:26239482.
- PMCID: PMC4551658.
- DOI: 10.1002/oby.21163


Abstract

Objective
Caffeine and ephedrine was an effective combination therapy for weight loss until ephedrine was removed from the market due to safety concerns. This study investigated the combination of caffeine and albuterol as a possibly safer alternative to ephedrine.

Methods
In a series of experiments using cultured adipocytes, rat models, and humans, the effects of caffeine and albuterol on lipolysis, metabolic rate, food intake, and body composition were evaluated.

Results
Both caffeine and albuterol enhanced lipolysis in cultured adipocytes. Acute treatment of humans with caffeine and/or albuterol increased resting metabolic rate. Longer‐term studies of rats revealed a trend for increased metabolic rate with albuterol treatment. There was increased lean mass gain concurrent with decreased fat mass gain with caffeine/albuterol treatment that was greater than albuterol treatment alone.

Conclusions
In rats, albuterol with caffeine produced significantly greater increases in lean body mass and reductions in fat mass without changes in food intake after 4‐8 weeks of treatment. Since caffeine and albuterol are approved for the treatment of asthma in children and adolescents at the doses tested and change body composition without changing food intake, this combination may deserve further exploration for use in treating pediatric obesity.

Original document

Parameters

Science
Research / Study
Date
4 August 2015
People
Arceneaux, Kenneth P. III
Chu, Jessica T.
Greenway, Frank L.
Jacob, Gregory Jr.
Johnson, William D.
Liu, Ann G.
Primeaux, Stefany D.
Schreiber, Allyson L.
Tipton, Russel C.
Yu, Ying
Country
United States of America
Language
English
Other organisations
Louisiana State University Health Sciences Center New Orleans
Pennington Biomedical Research Center (PBRC)
Doping classes
S3. Beta-2 Agonists
S6. Stimulants
Substances
Caffeine
Salbutamol
Document category
Scientific article
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Date generated
19 November 2019
Date of last modification
21 November 2019
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