Investigation of the Inhibitory Effects of the Benzodiazepine Derivative, 5-BDBD on P2X4 Purinergic Receptors by two Complementary Methods

• Main Authors: Bernadett Balázs, Tamás Dankó, Gergely Kovács, László Köles, Matthias A. Hediger, Ákos Zsembery
• Format: Article
• Language: English
• Published: Cell Physiol Biochem Press GmbH & Co KG 2013-07-01
• Series: Cellular Physiology and Biochemistry
• Subjects: 5-BDBD; P2X receptors; Calcium infux; Electrophysiology; ATP
• Online Access: http://www.karger.com/Article/FullText/350119
• ISSN: 1015-8987; 1421-9778

Background/Aims: ATP-gated P2X4 purinergic receptors (P2X4Rs) are cation channels with important roles in diverse cell types. To date, lack of specific inhibitors has hampered investigations on P2X4Rs. Recently, the benzodiazepine derivative, 5-BDBD has been proposed to selectively inhibit P2X4Rs. However, limited evidences are currently available on its inhibitory properties. Thus, we aimed to characterize the inhibitory effects of 5-BDBD on recombinant human P2X4Rs. Methods: We investigated ATP-induced intracellular Ca2+ signals and whole cell ion currents in HEK 293 cells that were either transiently or stably transfected with hP2X4Rs. Results: Our data show that ATP (4R-mediated Ca2+ influx while endogenously expressed P2Y receptors are not activated to any significant extent. Both 5-BDBD and TNP-ATP inhibit ATP-induced Ca2+ signals and inward ion currents in a concentration-dependent manner. Application of two different concentrations of 5-BDBD causes a rightward shift in ATP dose-response curve. Since the magnitude of maximal stimulation does not change, these data suggest that 5-BDBD may competitively inhibit the P2X4Rs. Conclusions: Our results demonstrate that application of submicromolar ATP concentrations allows reliable assessment of recombinant P2XR functions in HEK 293 cells. Furthermore, 5-BDBD and TNP-ATP have similar inhibitory potencies on the P2X4Rs although their mechanisms of actions are different.