AJP - Endo Information on EB 2010
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Am J Physiol Endocrinol Metab (August 23, 2005). doi:10.1152/ajpendo.00240.2005
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
290/1/E42    most recent
00240.2005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 Rasouli, N.
Right arrow Articles by Kern, P. A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rasouli, N.
Right arrow Articles by Kern, P. A
Submitted on May 31, 2005
Accepted on August 16, 2005

Increased Plasma Adiponectin in Response to Pioglitazone Does Not Result from Increased Gene Expression

Neda Rasouli1, Aiwei Yao-Borengasser1, Leslie M Miles1, Steven C Elbein1, and Philip A Kern1*

1 Division of Endocrinology, Central Arkansas Veterans Healthcare System, and University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA

* To whom correspondence should be addressed. E-mail: Kernphilipa{at}uams.edu.

Plasma levels of adiponectin are lower in obese and insulin resistant subjects compared to lean and insulin sensitive ones. Thiazolidinediones increase plasma adiponectin levels in diabetic subjects; although the mechanism of this increased plasma adiponectin has not been well studied. In the present study, we compared the plasma levels and adipose tissue expression of adiponectin in subjects with normal (NGT) and impaired glucose tolerance (IGT) and also studied the effects of metformin and. pioglitazone on plasma and adipose tissue mRNA level of adiponectin in IGT subjects. IGT subjects had lower plasma adiponectin levels compared to NGT subjects and similarly IGT subjects had lower adiponectin mRNA levels. In contrast, the increased plasma levels of adiponectin in response to pioglitazone were not associated with increased adiponectin expression in adipose tissue. Metformin did not cause any change in plasma or expression levels of adiponectin. Other adipokines were examined, and both pioglitazone and metformin decreased plasma levels of resistin in IGT subjects and pioglitazone (but not metformin) decreased plasma levels of leptin. These data suggest that pioglitazone increases plasma adiponectin levels by post-transcriptional regulation in contrast to transcriptional regulation of adiponectin in relation to insulin sensitivity in NGT vs. IGT subjects.




This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
N. Rasouli, A. Yao-Borengasser, V. Varma, H. J. Spencer, R. E. McGehee Jr, C. A. Peterson, J. L. Mehta, and P. A. Kern
Association of Scavenger Receptors in Adipose Tissue With Insulin Resistance in Nondiabetic Humans
Arterioscler Thromb Vasc Biol, September 1, 2009; 29(9): 1328 - 1335.
[Abstract] [Full Text] [PDF]


Home page
Eur J EndocrinolHome page
Z. Kovacova, M. Vitkova, M. Kovacikova, E. Klimcakova, M. Bajzova, Z. Hnevkovska, L. Rossmeislova, V. Stich, D. Langin, and J. Polak
Secretion of adiponectin multimeric complexes from adipose tissue explants is not modified by very low calorie diet
Eur. J. Endocrinol., April 1, 2009; 160(4): 585 - 592.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
A. Banga, R. Unal, P. Tripathi, I. Pokrovskaya, R. J. Owens, P. A. Kern, and G. Ranganathan
Adiponectin translation is increased by the PPAR{gamma} agonists pioglitazone and {omega}-3 fatty acids
Am J Physiol Endocrinol Metab, March 1, 2009; 296(3): E480 - E489.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
S. K. Das, W. S. Chu, A. K. Mondal, N. K. Sharma, P. A. Kern, N. Rasouli, and S. C. Elbein
Effect of pioglitazone treatment on endoplasmic reticulum stress response in human adipose and in palmitate-induced stress in human liver and adipose cell lines
Am J Physiol Endocrinol Metab, August 1, 2008; 295(2): E393 - E400.
[Abstract] [Full Text] [PDF]


Home page
Eur J EndocrinolHome page
L. Hojbjerre, M. Rosenzweig, F. Dela, J. M Bruun, and B. Stallknecht
Acute exercise increases adipose tissue interstitial adiponectin concentration in healthy overweight and lean subjects
Eur. J. Endocrinol., November 1, 2007; 157(5): 613 - 623.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
L. Qiang, H. Wang, and S. R. Farmer
Adiponectin Secretion Is Regulated by SIRT1 and the Endoplasmic Reticulum Oxidoreductase Ero1-L{alpha}
Mol. Cell. Biol., July 1, 2007; 27(13): 4698 - 4707.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
Z. V. Wang, T. D. Schraw, J.-Y. Kim, T. Khan, M. W. Rajala, A. Follenzi, and P. E. Scherer
Secretion of the Adipocyte-Specific Secretory Protein Adiponectin Critically Depends on Thiol-Mediated Protein Retention
Mol. Cell. Biol., May 15, 2007; 27(10): 3716 - 3731.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
S. Nakano, Y. Inada, H. Masuzaki, T. Tanaka, S. Yasue, T. Ishii, N. Arai, K. Ebihara, K. Hosoda, K. Maruyama, et al.
Bezafibrate regulates the expression and enzyme activity of 11beta-hydroxysteroid dehydrogenase type 1 in murine adipose tissue and 3T3-L1 adipocytes
Am J Physiol Endocrinol Metab, April 1, 2007; 292(4): E1213 - E1222.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
A. M. Bodles, A. Banga, N. Rasouli, F. Ono, P. A. Kern, and R. J. Owens
Pioglitazone increases secretion of high-molecular-weight adiponectin from adipocytes
Am J Physiol Endocrinol Metab, November 1, 2006; 291(5): E1100 - E1105.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2005 by the American Physiological Society.