scholarly journals The G protein‐coupled oestrogen receptor, GPER1, mediates direct anti‐inflammatory effects of oestrogens in human cholinergic neurones from the nucleus basalis of Meynert

2020 ◽  
Vol 32 (3) ◽  
Author(s):  
Erica Sarchielli ◽  
Giulia Guarnieri ◽  
Eglantina Idrizaj ◽  
Roberta Squecco ◽  
Tommaso Mello ◽  
...  
Author(s):  
Georg Gruenbacher ◽  
Hubert Gander ◽  
Gabriele Dobler ◽  
Andrea Rahm ◽  
Dominik Klaver ◽  
...  

2020 ◽  
Vol 277 (4) ◽  
pp. 1121-1127
Author(s):  
Saime Sagiroglu ◽  
Metin Kılınc ◽  
Adem Doganer ◽  
Nagihan Bilal ◽  
Israfil Orhan ◽  
...  

Andrologia ◽  
2020 ◽  
Vol 52 (10) ◽  
Author(s):  
Osman Barut ◽  
Muhammed Seyithanoglu ◽  
Faruk Kucukdurmaz ◽  
Bekir Turkay Demir ◽  
Caner Olmez ◽  
...  

2013 ◽  
Vol 591 (17) ◽  
pp. 4223-4235 ◽  
Author(s):  
G. Cristina Brailoiu ◽  
Khalid Benamar ◽  
Jeffrey B. Arterburn ◽  
Erhe Gao ◽  
Joseph E. Rabinowitz ◽  
...  

2017 ◽  
Vol 137 (10) ◽  
pp. S293
Author(s):  
M. Fábián ◽  
P. Balogh ◽  
F. Rencz ◽  
V. Brodszky ◽  
J. Hársing ◽  
...  

2004 ◽  
Vol 57 (9) ◽  
pp. 855 ◽  
Author(s):  
David P. Fairlie

Small molecules designed to mimic specific structural components of a protein (peptide strands, sheets, turns, helices, or amino acids) can be expected to display agonist or antagonist biological responses by virtue of interacting with the same receptors that recognize the protein. Here we describe some minimalist approaches to structural mimetics of amino acids and of strand, turn, or helix segments of proteins. The designed molecules show potent and selective inhibition of protease, transferase, and phospholipase enzymes, or antagonism of G-protein coupled or transcriptional receptors, and have potent anti-tumour, anti-inflammatory, or antiviral activity.


2017 ◽  
Vol 2017 ◽  
pp. 1-16 ◽  
Author(s):  
Ting Zhang ◽  
Malgorzata A. Garstka ◽  
Ke Li

After the discovery of the C5a receptor C5aR1, C5aR2 is the second receptor found to bind C5a and its des-arginine form. As a heptahelical G protein-coupled receptor but devoid of the intracellular Gα signal, C5aR2 is special and confusing. Ramifications and controversies about C5aR2 are under debate since its identification, from putative ligands and cellular localization to intracellular signals and pathological roles in inflammation and immunity. The ruleless and even conflicting pro- or anti-inflammatory role of C5aR2 in animal models of diverse diseases makes one bewildered. This review summarizes reports on C5aR2, tries to clear up available evidence on these four controversial aspects, and delineates C5aR2 function(s). It also summarizes available toolboxes for C5aR2 study.


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