Dihydropyridines Potentiate ATP-Induced Currents Mediated by the Full-Length Human P2X5 Receptor

• Published in: Molecules (Basel, Switzerland) Vol. 27; no. 6; p. 1846
• Main Authors: Schiller, Ida C, Jacobson, Kenneth A, Wen, Zhiwei, Malisetty, Aparna, Schmalzing, Günther, Markwardt, Fritz
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 11.03.2022; MDPI
• Subjects: Adenosine Triphosphate - pharmacology; Antagonists; ATP; Bacterial diseases; Bone loss; Bone tumors; dihydropyridines; Dihydropyridines - pharmacology; Gametocytes; HEK293 Cells; Humans; Inflammasomes; Inflammation; Kinetics; Leukemia; Ligands; Microelectrodes; Nimodipine; Oocytes; P2X5 receptor; Patch-Clamp Techniques; Permeability; Purine receptors; purinergic receptor; Receptors, Purinergic; voltage clamp; Xenopus oocytes; Xenopus oocytes; purinergic receptor; voltage clamp; dihydropyridines; P2X5 receptor
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules27061846

The P2X5 receptor, an ATP-gated cation channel, is believed to be involved in tumor development, inflammatory bone loss and inflammasome activation after bacterial infection. Therefore, it is a worthwhile pharmacological target to treat the corresponding diseases, especially in minority populations that have a gene variant coding for functional homotrimeric P2X5 channels. Here, we investigated the effects of dihydropyridines on the human full-length P2X5 receptor (hP2X5 ) heterologously expressed in oocytes using the two-microelectrode voltage clamp method. Agonist dependency, kinetics and permeation behavior, including Cl permeability, were similar to hP2X5 expressed in HEK293 or 1321N1 cells. Additionally, 1,4-dihydropyridines have been shown to interact with various other purinergic receptors, and we have examined them as potential hP2X5 modulators. Of seven commercially available and four newly synthesized dihydropyridines tested at hP2X5 , only amlodipine exerted an inhibitory effect, but only at a high concentration of 300 µM. Isradipine and-even more-nimodipine stimulated ATP-induced currents in the low micromolar range. We conclude that common dihydropyridines or four new derivatives of amlodipine are not suitable as hP2X5 antagonists, but amlodipine might serve as a lead for future synthesis to increase its affinity. Furthermore, a side effect of nimodipine therapy could be a stimulatory effect on inflammatory processes.