Histamine release, an undesired effect of thrombin inhibitors with basic character, is mediated through direct activation of G(i) proteins

• Published in: European journal of pharmacology 2006-05, Vol.538 (1-3), p.182-187
• Main Authors: Stempelj, Mateja, Zorko, Matjaz, Peternel, Luka, Urleb, Uros, Ferjan, Ilonka
• Format: Article
• Language: English
• Subjects: Analysis of Variance; Aniline Compounds - chemical synthesis; Aniline Compounds - pharmacology; Animals; Cell Survival - drug effects; Cells, Cultured; Dose-Response Relationship, Drug; GTP-Binding Protein alpha Subunits, Gi-Go - metabolism; Guanosine 5'-O-(3-Thiotriphosphate) - metabolism; Histamine - metabolism; Histamine Release - drug effects; Male; Mast Cells - cytology; Mast Cells - drug effects; Mast Cells - metabolism; Naphthalenes - chemical synthesis; Naphthalenes - pharmacology; Pertussis Toxin - pharmacology; Phenylalanine - analogs & derivatives; Phenylalanine - chemical synthesis; Phenylalanine - pharmacology; Protein Binding - drug effects; Rats; Rats, Wistar; Structure-Activity Relationship; Thrombin - antagonists & inhibitors
• ISSN: 0014-2999
• DOI: 10.1016/j.ejphar.2006.03.066

The common structural feature of LK direct thrombin inhibitors is a strong basic group attached to the azaphenylalanine scaffold, which is important for the appropriate interaction at the thrombin active site. Our previous results have shown that this basic group could be responsible for a reduction of tracheal air flow and a fall of mean arterial pressure in anaesthetized rats, an undesired effect of direct thrombin inhibitors which correlated with their ability to release histamine from mast cells. In the present study, we investigated the mechanism of LK direct thrombin inhibitors-induced histamine release from rat peritoneal mast cells. We demonstrated that thrombin inhibitors with basic character (LK-732, LK-639 and LK-6063) provoked release of histamine from mast cells, while less basic analogs (LK-658, LK-633 and LK-6062) had no effect. Histamine released by LK-732 and LK-639 was suppressed by removal of sialic acid residues by neuraminidase and by pertussis toxin, an inhibitor of G(i) protein activity. Additional demonstration that G proteins are the targets of LK-732 and LK-639 was provided by the increase of GTPgammaS binding rate to G proteins in rat brain cortical membranes. Our results indicate that basic direct thrombin inhibitors LK-732 and LK-639 provoke release of histamine from mast cells by direct activation of G(i) proteins through the similar biochemical pathway as basic secretagogues.