| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
ARTICLES |
Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808
Address all correspondence and requests for reprints to: Ruth Harris, Ph.D., Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, Louisiana 70808. E-mail: harrisrb{at}mhs.pbrc.edu
Genetically obese C57Bl/6J-m db/db mice were parabiosed with either lean male db/+ or obese female ob/ob mice. Male db/db mice had lower serum leptin than females, and this was reflected in the amount of protein that crossed the parabiotic union into their partners. Eighteen days post operation, ob/ob partners of db/db mice had increased body temperature, lost 50% body weight and 60% body fat, but maintained carcass protein. The db/+ partners of db/db mice had a normal gut content and (by implication) food intake, did not raise their body temperature, but lost significant amounts of both lean and fat tissue during 25 days of parabiosis. The differences between the db/+ and ob/ob partners of db/db mice may be caused by leptin inhibiting growth of male mice, but not of female mice that are on a slower growth curve, or by the excess lipid in ob/ob mice sparing body protein. The db/db partners of ob/ob mice lost a small amount of body fat, but carcass protein was increased by 30%, compared with their controls. These results imply that leptin stimulated release of a circulating growth factor, possibly through activation of the long-form leptin receptor, in ob/ob partners of db/db mice.
This article has been cited by other articles:
![]() |
T. J. Bartness and C. K. Song Thematic review series: Adipocyte Biology. Sympathetic and sensory innervation of white adipose tissue J. Lipid Res., August 1, 2007; 48(8): 1655 - 1672. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Abe, C. Boyer, X. Liu, F. Q. Wen, T. Kobayashi, Q. Fang, X. Wang, M. Hashimoto, J. G. Sharp, and S. I. Rennard Cells Derived from the Circulation Contribute to the Repair of Lung Injury Am. J. Respir. Crit. Care Med., December 1, 2004; 170(11): 1158 - 1163. [Abstract] [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
C. H. Wiegman, R. H.J. Bandsma, M. Ouwens, F. H. van der Sluijs, R. Havinga, T. Boer, D.-J. Reijngoud, J. A. Romijn, and F. Kuipers Hepatic VLDL Production in ob/ob Mice Is Not Stimulated by Massive De Novo Lipogenesis but Is Less Sensitive to the Suppressive Effects of Insulin Diabetes, May 1, 2003; 52(5): 1081 - 1089. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Madiehe, S. Hebert, T. D. Mitchell, and R. B. S. Harris Strain-Dependent Stimulation of Growth in Leptin-Treated Obese db/db Mice Endocrinology, October 1, 2002; 143(10): 3875 - 3883. [Abstract] [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
G. E. Truett, J. A. Walker, and R. B. S. Harris A developmental switch affecting growth of fatty rats Am J Physiol Regulatory Integrative Comp Physiol, December 1, 2000; 279(6): R1956 - R1963. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |