AJCN North Carolina Research Campus
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Westerterp-Plantenga, M. S
Right arrow Articles by Campfield, L A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Westerterp-Plantenga, M. S
Right arrow Articles by Campfield, L A.
Agricola
Right arrow Articles by Westerterp-Plantenga, M. S
Right arrow Articles by Campfield, L A.
American Journal of Clinical Nutrition, Vol. 74, No. 4, 426-434, October 2001
© 2001 American Society for Clinical Nutrition


Original Research Communication

Effects of weekly administration of pegylated recombinant human OB protein on appetite profile and energy metabolism in obese men1,2,3

Margriet S Westerterp-Plantenga, Wim HM Saris, Chris J Hukshorn and L Arthur Campfield

1 From the Department of Human Biology, Maastricht University, Maastricht, Netherlands, and the Department of Food Science and Human Nutrition, Colorado State University, Fort Collins.

Background: Results of leptin administration in mice, rats, and humans provide a rationale for therapeutic augmentation of circulating leptin (OB protein) concentrations in obese humans; this may reduce food intake, increase metabolic rate, and lower body mass.

Objective: We assessed the effects of weekly subcutaneous pegylated polyethylene glycol (PEG)-OB protein administration on appetite and energy metabolism in obese men.

Design: We performed a randomized, double-blind, placebo-controlled trial in 30 obese men [body mass index (in kg/m2): 34.2 ± 3.6; age: 44.7 ± 7 y]. Subjects received 20 mg PEG-OB protein/wk for 12 wk while limiting their energy intake to 2.1 MJ/d.

Results: During treatment, appetite and hunger before breakfast decreased and remained lower in the PEG-OB-protein group, whereas they increased and remained higher in the placebo group (P < 0.0001). During treatment, hunger decreased in the PEG-OB-protein group (P < 0.05) and cognitive restraint increased in the placebo group (P < 0.0001). Neither appetite nor food intake changed significantly during the ad libitum evening meal. Under energy balance conditions in the respiration chamber, appetite at the end of treatment was not significantly different from baseline despite similar, significant reductions in 24-h energy intake, energy expenditure, sleeping metabolic rate, body mass, fat mass, and fat-free mass (P < 0.01 for all) in both groups.

Conclusion: Treatment with PEG-OB protein modified subjective appetite at a dosage that produced no changes in body composition, energy expenditure, or body mass loss relative to placebo treatment, suggesting that PEG-OB protein has central rather than peripheral biological activity in obese men.

Key Words: Obesity • leptin • OB protein • PEG-OB protein • appetite • respiration chamber • universal eating monitor • energy balance • hunger • satiety • food intake • underreporting • energy expenditure • body mass • body composition • weight reduction • weight loss




This article has been cited by other articles:


Home page
Ann. N. Y. Acad. Sci.Home page
K. L. KNUTSON and E. VAN CAUTER
Associations between Sleep Loss and Increased Risk of Obesity and Diabetes
Ann. N.Y. Acad. Sci., May 1, 2008; 1129(1): 287 - 304.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
P. Cottone, V. Sabino, T. R. Nagy, D. V. Coscina, and E. P. Zorrilla
Feeding microstructure in diet-induced obesity susceptible versus resistant rats: central effects of urocortin 2
J. Physiol., September 1, 2007; 583(2): 487 - 504.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
G. G. Gosman, H. I. Katcher, and R. S. Legro
Obesity and the role of gut and adipose hormones in female reproduction
Hum. Reprod. Update, September 1, 2006; 12(5): 585 - 601.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
M. Mars, C. de Graaf, L. C. de Groot, and F. J Kok
Decreases in fasting leptin and insulin concentrations after acute energy restriction and subsequent compensation in food intake
Am. J. Clinical Nutrition, March 1, 2005; 81(3): 570 - 577.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
R. Ahima and S. Y. Osei
Leptin and Appetite Control in Lipodystrophy
J. Clin. Endocrinol. Metab., September 1, 2004; 89(9): 4254 - 4257.
[Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
C. de Graaf, W. A. Blom, P. A. Smeets, A. Stafleu, and H. F. Hendriks
Biomarkers of satiation and satiety
Am. J. Clinical Nutrition, June 1, 2004; 79(6): 946 - 961.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
E. Doucet, M. Pomerleau, and M.-E. Harper
Fasting and Postprandial Total Ghrelin Remain Unchanged after Short-Term Energy Restriction
J. Clin. Endocrinol. Metab., April 1, 2004; 89(4): 1727 - 1732.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
C. J. Hukshorn, J. H. N. Lindeman, K. H. Toet, W. H. M. Saris, P. H. C. Eilers, M. S. Westerterp-Plantenga, and T. Kooistra
Leptin and the Proinflammatory State Associated with Human Obesity
J. Clin. Endocrinol. Metab., April 1, 2004; 89(4): 1773 - 1778.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
P. J. Havel
Update on Adipocyte Hormones: Regulation of Energy Balance and Carbohydrate/Lipid Metabolism
Diabetes, February 1, 2004; 53(90001): S143 - 151.
[Abstract] [Full Text]


Home page
DiabetesHome page
C. Anderwald, G. Brabant, E. Bernroider, R. Horn, A. Brehm, W. Waldhausl, and M. Roden
Insulin-Dependent Modulation of Plasma Ghrelin and Leptin Concentrations Is Less Pronounced in Type 2 Diabetic Patients
Diabetes, July 1, 2003; 52(7): 1792 - 1798.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
C. J Hukshorn, M. S Westerterp-Plantenga, and W. H. Saris
Pegylated human recombinant leptin (PEG-OB) causes additional weight loss in severely energy-restricted, overweight men
Am. J. Clinical Nutrition, April 1, 2003; 77(4): 771 - 776.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
S. S Elliott, N. L Keim, J. S Stern, K. Teff, and P. J Havel
Fructose, weight gain, and the insulin resistance syndrome
Am. J. Clinical Nutrition, November 1, 2002; 76(5): 911 - 922.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by The American Society for Nutrition