| Literature DB >> 27234891 |
Sofia Vasilakaki1, Efrosini Barbayianni1, Victoria Magrioti1, Oleksandr Pastukhov2, Violetta Constantinou-Kokotou3, Andrea Huwiler2, George Kokotos4.
Abstract
The upregulation of PGE2 by mesangial cells has been observed under chronic inflammation condition. In the present work, renal mesangial cells were stimulated to trigger a huge increase of PGE2 synthesis and were treated in the absence or presence of known PLA2 inhibitors. A variety of synthetic inhibitors, mainly developed in our labs, which are known to selectively inhibit each of GIVA cPLA2, GVIA iPLA2, and GIIA/GV sPLA2, were used as tools in this study. Synthetic sPLA2 inhibitors, such as GK115 (an amide derivative based on the non-natural amino acid (R)-γ-norleucine) as well as GK126 and GK241 (2-oxoamides based on the natural (S)-α-amino acid leucine and valine, respectively) presented an interesting effect on the suppression of PGE2 formation.Entities:
Keywords: Inhibitors; Mesangial cells; Phospholipase A(2); Prostaglandin E(2); Secreted phospholipase A(2)
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Year: 2016 PMID: 27234891 DOI: 10.1016/j.bmc.2016.05.017
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641