AJP - Regu Journal of Neurophysiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol 293: R1855-R1863, 2007. First published September 12, 2007; doi:10.1152/ajpregu.00297.2007
0363-6119/07 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
293/5/R1855    most recent
00297.2007v1
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 Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mack, C.
Right arrow Articles by Parkes, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mack, C.
Right arrow Articles by Parkes, D.

APPETITE, OBESITY, DIGESTION, AND METABOLISM

Pharmacological actions of the peptide hormone amylin in the long-term regulation of food intake, food preference, and body weight

Christine Mack, Julie Wilson, Jennifer Athanacio, James Reynolds, Kevin Laugero, Stacy Guss, Calvin Vu, Jonathan Roth, and David Parkes

Amylin Pharmaceuticals, Inc., San Diego, California

Submitted 27 April 2007 ; accepted in final form 7 September 2007

The ability of amylin to reduce acute food intake in rodents is well established. Longer-term administration in rats (up to 24 days) shows a concomitant reduction in body weight, suggesting energy intake plays a significant role in mediating amylin-induced weight loss. The current set of experiments further explores the long-term effects of amylin (4–11 wk) on food preference, energy expenditure, and body weight and composition. Furthermore, we describe the acute effect of amylin on locomotor activity and kaolin consumption to test for possible nonhomeostatic mechanisms that could affect food intake. Four-week subcutaneous amylin infusion of high-fat fed rats (3–300 µg·kg–1·day–1) dose dependently reduced food intake and body weight gain (ED50 for body weight gain = 16.5 µg·kg–1·day–1). The effect of amylin on body weight gain was durable for up to 11 wks and was associated with a specific loss of fat mass and increased metabolic rate. The body weight of rats withdrawn from amylin (100 µg·kg–1·day–1) after 4 wks of infusion returned to control levels 2 wks after treatment cessation, but did not rebound above control levels. When self-selecting calories from a low- or high-fat diet during 11 wks of infusion, amylin-treated rats (300 µg·kg–1·day–1) consistently chose a larger percentage of calories from the low-fat diet vs. controls. Amylin acutely had no effect on locomotor activity or kaolin consumption at doses that decreased food intake. These results demonstrate pharmacological actions of amylin in long-term body weight regulation in part through appetitive-related mechanisms and possibly via changes in food preference and energy expenditure.

body composition; meal size; locomotor activity; kaolin consumption; pramlintide



Address for reprint requests and other correspondence: C. Mack, Amylin Pharmaceuticals, Inc., 9360 Towne Centre Dr., San Diego, CA 92121 (e-mail: christine.mack{at}amylin.com)




This article has been cited by other articles:


Home page
Arch NeurolHome page
J. D. Roth, H. Maier, S. Chen, and B. L. Roland
Implications of Amylin Receptor Agonism: Integrated Neurohormonal Mechanisms and Therapeutic Applications
Arch Neurol, March 1, 2009; 66(3): 306 - 310.
[Full Text] [PDF]


Home page
Diabetes CareHome page
S. R. Smith, L. J. Aronne, C. M. Burns, N. C. Kesty, A. E. Halseth, and C. Weyer
Sustained Weight Loss Following 12-Month Pramlintide Treatment as an Adjunct to Lifestyle Intervention in Obesity
Diabetes Care, September 1, 2008; 31(9): 1816 - 1823.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
R. D. Reidelberger, A. C. Haver, P. K. Chelikani, and J. L. Buescher
Effects of different intermittent peptide YY (3-36) dosing strategies on food intake, body weight, and adiposity in diet-induced obese rats
Am J Physiol Regulatory Integrative Comp Physiol, August 1, 2008; 295(2): R449 - R458.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.