AJP - Regu AJP: Lung Cellular and Molecular Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol 272: R1800-R1808, 1997;
0363-6119/97 $5.00
This Article
Right arrow Full Text (PDF)
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 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 Harris, R. B.
Right arrow Articles by Kuijper, J. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Harris, R. B.
Right arrow Articles by Kuijper, J. L.

AJP - Regulatory, Integrative and Comparative Physiology, Vol 272, Issue 6 1800-R1808, Copyright © 1997 by American Physiological Society


ARTICLES

Recombinant leptin exchanges between parabiosed mice but does not reach equilibrium

R. B. Harris, J. Zhou, D. S. Weigle and J. L. Kuijper
Neuroscience Department, Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808, USA.

Parabiosis experiments suggest that ob/ob mice are deficient in a circulating "lipostatic" signal but respond to such a signal when it is delivered in the cross circulation from their parabiotic partner. Identification of leptin as the mutation in ob/ob mice leads to the assumption that leptin is the lipostatic signal. The objective of these experiments was to determine the circulating half-life of leptin and to demonstrate whether it exchanged between parabiosed mice. Measurement of disappearance of recombinant leptin from serum in SWRJ mice indicated a circulating half-life of approximately 36 min. Single ob/ob mice or one member of a parabiosed pair of ob/ob mice received 50 micrograms recombinant murine leptin in two intraperitoneal injections a day for 10 days, starting 40 days after parabiosis surgery. Control mice and pairs received equivalent injections of vehicle. In single mice, leptin significantly reduced food intake, body weight, serum insulin, and pancreatic and liver weight. Leptin treatment of one member of a parabiosed pair of ob/ob mice reduced serum insulin, gut content (an index of food intake), and body fat in both partners. The injected parabiont lost more fat than its partner, and body temperature was increased only in the injected mouse, indicating that leptin did not reach equilibrium in the two animals. This was confirmed by Western blot analysis of serum leptin measured 2 h after injection. Therefore, although leptin can exchange between parabionts, its half-life is inadequate to allow equilibrium when a large concentration gradient exists between partners.


This article has been cited by other articles:


Home page
J. Appl. Physiol.Home page
R. A. Johnston, T. A. Theman, R. D. Terry, E. S. Williams, and S. A. Shore
Pulmonary responses to acute ozone exposure in fasted mice: effect of leptin administration
J Appl Physiol, January 1, 2007; 102(1): 149 - 156.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
D. M. Penn, L. C. Jordan, E. W. Kelso, J. E. Davenport, and R. B. S. Harris
Effects of central or peripheral leptin administration on norepinephrine turnover in defined fat depots
Am J Physiol Regulatory Integrative Comp Physiol, December 1, 2006; 291(6): R1613 - R1621.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
C. Rooks, T. Bennet, T. J. Bartness, and R. B. S. Harris
Compensation for an increase in body fat caused by donor transplants into mice
Am J Physiol Regulatory Integrative Comp Physiol, June 1, 2004; 286(6): R1149 - R1155.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
H. Bowen, T. D. Mitchell, and R. B. S. Harris
Method of leptin dosing, strain, and group housing influence leptin sensitivity in high-fat-fed weanling mice
Am J Physiol Regulatory Integrative Comp Physiol, January 1, 2003; 284(1): R87 - R100.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
R. B. S. Harris, D. B. Hausman, and T. J. Bartness
Compensation for partial lipectomy in mice with genetic alterations of leptin and its receptor subtypes
Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2002; 283(5): R1094 - R1103.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
G. FRUHBECK and J. GOMEZ-AMBROSI
Rationale for the existence of additional adipostatic hormones
FASEB J, September 1, 2001; 15(11): 1996 - 2006.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
R. B. S. Harris, T. D. Mitchell, X. Yan, J. S. Simpson, and S. M. Redmann Jr.
Metabolic responses to leptin in obese db/db mice are strain dependent
Am J Physiol Regulatory Integrative Comp Physiol, July 1, 2001; 281(1): R115 - R132.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online