Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011:2011:210484.
doi: 10.1155/2011/210484. Epub 2010 Aug 12.

Assessment of acute and chronic pharmacological effects on energy expenditure and macronutrient oxidation in humans: responses to ephedrine

Affiliations

Assessment of acute and chronic pharmacological effects on energy expenditure and macronutrient oxidation in humans: responses to ephedrine

Antonella Napolitano et al. J Obes. 2011.

Abstract

Evidence of active brown adipose tissue in human adults suggests that this may become a pharmacological target to induce negative energy balance. We have explored whole-body indirect calorimetry to detect the metabolic effects of thermogenic drugs through administration of ephedrine hydrochloride and have assessed ephedrine's merits as a comparator compound in the evaluation of novel thermogenic agents. Volunteers randomly given ephedrine hydrochloride 15 mg QID (n = 8) or placebo (n = 6) were studied at baseline and after 1-2 and 14-15 days of treatment. We demonstrate that overnight or 23-hour, 2% energy expenditure (EE) and 5% fat (FO) or CHO oxidation effects are detectable both acutely and over 14 days. Compared to placebo, ephedrine increased EE and FO rates overnight (EE 63 kJ day 2, EE 105 kJ, FO 190 kJ, day 14), but not over 23 h. We conclude that modest energy expenditure and fat oxidation responses to pharmacological interventions can be confidently detected by calorimetry in small groups. Ephedrine should provide reliable data against which to compare novel thermogenic compounds.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Mean differences and standard deviations of differences between measures of energy expenditure, made overnight and over 23 hours, and repeated after a 24-hour or 14-day interval. Untreated (placebo) subjects, n = 6.
Figure 2
Figure 2
Mean differences and standard deviations of differences between measures of fat, carbohydrate, and protein oxidation, made overnight and over 23 hours, and repeated after a 24-hour or 14-day interval. Untreated (placebo) subjects, n = 6.
Figure 3
Figure 3
Circulating concentrations of ephedrine hydrochloride in treated subjects (n = 8). Solid bars: days 1-2; hatched bars days: 14-15. T indicates administration times.
Figure 4
Figure 4
Influence on 22.5-hour average heart rate of acute or chronic (14 day) treatment with ephedrine hydrochloride (solid bars) or placebo (open bars).

Similar articles

Cited by

References

    1. Wadden TA, Berkowitz RI, Womble LG, et al. Randomized trial of lifestyle modification and pharmacotherapy for obesity. The New England Journal of Medicine. 2005;353(20):2111–2120. - PubMed
    1. Avenell A, Broom J, Brown TJ, et al. Systematic review of the long-term effects and economic consequences of treatments for obesity and implications for health improvement. Health Technology Assessment. 2004;8(21):1–182. - PubMed
    1. Dansinger ML, Tatsioni A, Wong JB, Chung M, Balk EM. Meta-analysis: the effect of dietary counseling for weight loss. Annals of Internal Medicine. 2007;147(1):41–50. - PubMed
    1. Astrup A, Breum L, Toubro S, Hein P, Quaade F. The effect and safety of an ephedrine/caffeine compound compared to ephedrine, caffeine and placebo in obese subjects on an energy restricted diet. A double blind trial. International Journal of Obesity and Related Metabolic Disorders. 1992;16(4):269–277. - PubMed
    1. Astrup A, Madsbad S, Breum L, Jensen TJ, Kroustrup JP, Larsen TM. Effect of tesofensine on bodyweight loss, body composition, and quality of life in obese patients: a randomised, double-blind, placebo-controlled trial. The Lancet. 2008;372(9653):1906–1913. - PubMed

LinkOut - more resources