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dc.date.accessioned2017-02-22T14:45:02Z
dc.date.available2017-02-22T14:45:02Z
dc.date.created2017-01-08T21:59:07Z
dc.date.issued2016
dc.identifier.urihttp://hdl.handle.net/10852/53971
dc.description.abstractThe peroxisome proliferator-activated receptors (PPARα, PPARβ/δ and PPARγ) are nuclear receptors whose target genes have fundamental roles in human health and disease. The PPAR-regulated expression of these genes influences a range of physiological processes, including cell differentiation and proliferation, inflammation and lipid metabolism. Thus, the ligand-dependent modulation of PPAR activity is a potential point of pharmacological intervention in e.g. metabolic-, neurodegenerative- and dermatologic diseases. Recent reports on the involvement of PPARβ/δ in the pathophysiologies of breast cancer and psoriasis, highlight this PPAR subtype as a target of particular interest. The effects of agonistic ligands on PPAR target gene expression have been studied for nearly two decades and a structurally diverse collection of agonists has been reported. In contrast, fewer PPAR antagonists have been reported and the knowlegde about their various modes of action is less developed than that of agonists. In this thesis, the development of new members of a class of covalent PPARβ/δ antagonists is presented. Our studies demonstrate that the selectivity of the new antagonists for PPARβ/δ could be increased through subtle modifications of the structure of a previously reported antagonist, without affecting its mode of action. In extension of these studies, an investigation into the modes of action of the reported antagonistic ligands of PPARβ/δ was undertaken. In this study, an emphasis was put on the possible involvement of covalent bond formation between PPARβ/δ and the antagonistic ligands. Through a series of chemical and biological assays, it could be demonstrated that the reported antagonistic ligands differ markedly in their modes of action. Our results thus contribute to a more nuanced classification of the studied PPARβ/δ ligands. Finally, the recent dicovery of a novel post-translational modification of PPARγ, has impacted on the understanding of the beneficial effects of PPARγ agonists as drugs to treat metabolic diseases. The nature of the ligand-dependent inhibition of this undesired regulatory event, has shifted the focus of PPARγ ligand development away from full agonists, towards the development of partial- and non-agonists. The large body of structural data from x-ray crystallography on PPARγ in complex with ligands displaying a diverse set of binding modes, permitted a collective analysis of these data, aiming to identify structural trends in the influences of the ligands on PPARγ. Our study employed principal component analyses of the atomic coordinates and dihedral angles of PPARγ. The results of this investigation demonstrate a separation of the PPARγ structures, corresponding to a varying degree of stabilization of a region of the protein, known to be important for the undesired biological effects of full agonists. Thus, our analysis provides a mapping of the PPARγ structures with potential utility in the development of new partial- and non-agonistic PPARγ ligands. Appendix B contains published scientific papers and are removed due to publisher restrictions.
dc.languageEN
dc.publisherFaculty of Mathematics and Natural Sciences, University of Oslo
dc.relation.haspartI. Synthesis, biological evaluation and molecular modeling studies of the PPARβ/δ antagonist CC618. Åsmund Kaupang, Steinar Martin Paulsen, Calin C. Steindal, Aina W. Ravna, Ingebrigt Sylte, Trine G. Halvorsen, G. Hege Thoresen, Trond Vidar Hansen European Journal of Medicinal Chemistry, 2015, 94, 229 - 236. The paper is not available in DUO due to publisher restrictions. The published version is available at: http://dx.doi.org/10.1016/j.ejmech.2015.03.006
dc.relation.haspartII. Synthesis of 5-trifluoromethyl-2-sulfonylpyridine PPARβ/δ antagonists: Effects on the affinity and selectivity towards PPARβ/δ. Åsmund Kaupang, Eili T. Kase, Cecilie Xuan Trang Vo, Marthe Amundsen, Anders Vik, Trond Vidar Hansen Bioorganic & Medicinal Chemistry, 2016, 24, 247 - 260. The paper is not available in DUO due to publisher restrictions. The published version is available at: http://dx.doi.org/10.1016/j.bmc.2015.12.012
dc.relation.haspartIII. Involvement of covalent interactions in the mode of action of PPARβ/δ antagonists. Åsmund Kaupang, Siri Hildonen, Trine G. Halvorsen, Magnus Mortén, Anders Vik, Trond Vidar Hansen RSC Advances, 2015, 5, 76483 - 76490. The paper is not available in DUO due to publisher restrictions. The published version is available at: http://dx.doi.org/10.1039/c5ra15707b
dc.relation.haspartIV. Structural review of PPARγ in complex with ligands: Cartesian and dihedral principal component analyses of x-ray crystallographic data. Åsmund Kaupang, Tuomo Laitinen, Antti Poso, Trond Vidar Hansen Manuscript To be published. The paper is not available in DUO awaiting publishing.
dc.relation.urihttp://dx.doi.org/10.1016/j.ejmech.2015.03.006
dc.relation.urihttp://dx.doi.org/10.1016/j.bmc.2015.12.012
dc.relation.urihttp://dx.doi.org/10.1039/c5ra15707b
dc.titleDevelopment of PPAR Modulators and Investigations on their Mode of Action
dc.typeDoctoral thesis
dc.creator.authorKaupang, Åsmund
cristin.unitcode185,15,0,0
cristin.unitnameDet matematisk-naturvitenskapelige fakultet
cristin.ispublishedtrue
cristin.fulltextoriginal
dc.identifier.cristin1422918
dc.identifier.pagecount308
dc.identifier.urnURN:NBN:no-57106
dc.type.documentDoktoravhandling
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/53971/4/PhD-Kaupang-DUO.pdf


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