JOE
HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


DOI: 10.1677/joe.0.1610511

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
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI 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 ISI Web of Science (23)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Isozaki, O
Right arrow Articles by Seki, H
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Isozaki, O
Right arrow Articles by Seki, H
Journal of Endocrinology, Vol 161, Issue 3, 511-516
Copyright © 1999 by Society for Endocrinology


Articles

Growth hormone directly inhibits leptin gene expression in visceral fat tissue in fatty Zucker rats

O Isozaki, T Tsushima, M Miyakawa, Y Nozoe, H Demura, and H Seki


Growth hormone (GH) is known to interact with adipose tissue and to induce lipolysis. Adipocytes produce leptin which regulates appetite and energy expenditure. In order to elucidate the role of GH in leptin production, we studied the effect of GH on leptin gene expression and body fat in fatty Zucker rats, a model of obesity with resistance to both leptin and insulin. Recombinant human GH administered subcutaneously at 0.5 mg/kg per day (low dose) as well as at 1.65 mg/kg per day (high dose) reduced leptin mRNA levels in epididymal fat tissue but not in subcutaneous fat tissue after 7 days. GH administration only at the high dose reduced percentage body fat. Insulin-like growth factor-I infusion (200 microg/kg per day) did not change percentage body fat or leptin mRNA levels in epididymal fat. These observations suggest that GH directly interacts with adipose tissue and reduces leptin gene expression in visceral fat tissue.


This article has been cited by other articles:


Home page
J. Histochem. Cytochem.Home page
C. Crane, N. Akhter, B. W. Johnson, M. Iruthayanathan, F. Syed, A. Kudo, Y.-H. Zhou, and G. V. Childs
Fasting and Glucose Effects on Pituitary Leptin Expression: Is Leptin a Local Signal for Nutrient Status?
J. Histochem. Cytochem., October 1, 2007; 55(10): 1059 - 1073.
[Abstract] [Full Text] [PDF]


Home page
J ANIM SCIHome page
T. G. Ramsay and M. P. Richards
Leptin and leptin receptor expression in skeletal muscle and adipose tissue in response to in vivo porcine somatotropin treatment
J Anim Sci, November 1, 2005; 83(11): 2501 - 2508.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
H. S. Randeva, R. D. Murray, K. C. Lewandowski, C. J. O'Callaghan, R. Horn, P. O'Hare, G. Brabant, E. W. Hillhouse, and S. M. Shalet
Differential Effects of GH Replacement on the Components of the Leptin System in GH-Deficient Individuals
J. Clin. Endocrinol. Metab., February 1, 2002; 87(2): 798 - 804.
[Abstract] [Full Text] [PDF]




HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the Society for Endocrinology.