JPET Assistant Professor of Medicine (Clinician-Educator)

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on July 31, 2003; DOI: 10.1124/jpet.103.052852


0022-3565/03/3071-291-296$20.00
JPET 307:291-296, 2003
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jpet.103.052852v1
307/1/291    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
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 Bramlett, K. S.
Right arrow Articles by Burris, T. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bramlett, K. S.
Right arrow Articles by Burris, T. P.

CELLULAR AND MOLECULAR

A Natural Product Ligand of the Oxysterol Receptor, Liver X Receptor

Kelli S. Bramlett, Keith A. Houck, Kristen M. Borchert, Michele S. Dowless, Palaniappan Kulanthaivel, Youyan Zhang, Thomas P. Beyer, Robert Schmidt, Jeffrey S. Thomas, Laura F. Michael, Robert Barr, Chahrzad Montrose, Patrick I. Eacho, Guoqing Cao, and Thomas P. Burris

Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, Indiana

Natural products have been identified as ligands for a number of members of the nuclear hormone receptor (NHR) superfamily. Often these natural products are used as dietary supplements to treat myriad ailments ranging from perimenopausal hot flashes to hypercholesterolemia and reduced cognitive function. Examples of some natural product ligands for NHRs include genestein (estrogen receptors NR3A1 and NR3A2), guggulsterone (farnesoid X receptor NR1H4), and St. John's wort (pregnane X receptor, NR1I2). In this study, we identified the first nonoxysterol natural product that functions as a ligand for the liver X receptor (LXR{alpha} and LXR{beta}; NR1H3, NR1H2), a NHR that acts as the receptor for oxysterols and plays a key role in regulation of cholesterol metabolism and transport as well as glucose metabolism. We show that paxilline, a fungal metabolite, is an efficacious agonist of both LXR{alpha} and LXR{beta} in biochemical and in vitro cell-based assays. Paxilline binds directly to both receptors and is an activator of LXR-dependent transcription in cell-based reporter assays. We also demonstrate that paxilline binding to the receptors results in efficient activation of transcription of two physiological LXR target genes, ABCA1 and SREBP. The discovery of paxilline, the first reported nonoxysterol natural product ligand of the LXRs, may provide insight into the mechanism of ligand recognition by these receptors and reaffirms the utility of examining natural product libraries for identifying novel NHR ligands.


Received April 8, 2003; accepted June 12, 2003.

Address correspondence to: Dr. Thomas P. Burris, Gene Regulation Research, DC0434, Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN 46060. E-mail: burris_thomas_p{at}lilly.com




This article has been cited by other articles:


Home page
J. Immunol.Home page
K. Smoak, J. Madenspacher, S. Jeyaseelan, B. Williams, D. Dixon, K. R. Poch, J. A. Nick, G. S. Worthen, and M. B. Fessler
Effects of Liver X Receptor Agonist Treatment on Pulmonary Inflammation and Host Defense
J. Immunol., March 1, 2008; 180(5): 3305 - 3312.
[Abstract] [Full Text] [PDF]


Home page
Pharmacol. Rev.Home page
D. D. Moore, S. Kato, W. Xie, D. J. Mangelsdorf, D. R. Schmidt, R. Xiao, and S. A. Kliewer
International Union of Pharmacology. LXII. The NR1H and NR1I Receptors: Constitutive Androstane Receptor, Pregnene X Receptor, Farnesoid X Receptor {alpha}, Farnesoid X Receptor beta, Liver X Receptor {alpha}, Liver X Receptor beta, and Vitamin D Receptor
Pharmacol. Rev., December 1, 2006; 58(4): 742 - 759.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
R. J. Schmidt, J. V. Ficorilli, Y. Zhang, K. S. Bramlett, T. P. Beyer, K. Borchert, M. S. Dowless, K. A. Houck, T. P. Burris, P. I. Eacho, et al.
A 15-ketosterol is a liver X receptor ligand that suppresses sterol-responsive element binding protein-2 activity
J. Lipid Res., May 1, 2006; 47(5): 1037 - 1044.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
T. P. Burris, C. Montrose, K. A. Houck, H. E. Osborne, W. P. Bocchinfuso, B. C. Yaden, C. C. Cheng, R. W. Zink, R. J. Barr, C. D. Hepler, et al.
The Hypolipidemic Natural Product Guggulsterone Is a Promiscuous Steroid Receptor Ligand
Mol. Pharmacol., March 1, 2005; 67(3): 948 - 954.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
R. S. Savkur, J. S. Thomas, K. S. Bramlett, Y. Gao, L. F. Michael, and T. P. Burris
Ligand-Dependent Coactivation of the Human Bile Acid Receptor FXR by the Peroxisome Proliferator-Activated Receptor {gamma} Coactivator-1{alpha}
J. Pharmacol. Exp. Ther., January 1, 2005; 312(1): 170 - 178.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 2003 by the American Society for Pharmacology and Experimental Therapeutics.