A1 Journal article – refereed
Selective Calcium-Dependent Inhibition of ATP-Gated P2X3 Receptors by Bisphosphonate-Induced Endogenous ATP Analog ApppI




List of Authors: Ishchenko Yevheniia, Shakirzyanova Anastasia, Giniatullina Raisa, Skorinkin Andrei, Bart Geneviev, Turhanen Petri, Määttä Jorma A, Monkkonen Jukka, Giniatullin Rashid
Publisher: AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
Publication year: 2017
Journal: Journal of Pharmacology and Experimental Therapeutics
Journal name in source: JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
Journal acronym: J PHARMACOL EXP THER
Volume number: 361
Issue number: 1
Number of pages: 10
ISSN: 0022-3565
eISSN: 1521-0103

Abstract
Pain is the most unbearable symptom accompanying primary bone cancers and bone metastases. Bone resorptive disorders are often associated with hypercalcemia, contributing to the pathologic process. Nitrogen-containing bisphosphonates (NBPs) are efficiently used to treat bone cancers and metastases. Apart from their toxic effect on cancer cells, NBPs also provide analgesia via poorly understood mechanisms. We previously showed that NBPs, by inhibiting the mevalonate pathway, induced formation of novel ATP analogs such as ApppI [1-adenosin-59-yl ester 3-(3-methylbut- 3-enyl) triphosphoric acid diester], which can potentially be involved in NBP analgesia. In this study, we used the patchclamp technique to explore the action of ApppI on native ATP-gated P2X receptors in rat sensory neurons and rat and human P2X3, P2X2, and P2X7 receptors expressed in human embryonic kidney cells. We found that although ApppI has weak agonist activity, it is a potent inhibitor of P2X3 receptors operating in the nanomolar range. The inhibitory action of ApppI was completely blocked in hypercalcemia-like conditions and was stronger in human than in rat P2X3 receptors. In contrast, P2X2 and P2X7 receptors were insensitive to ApppI, suggesting a high selectivity of ApppI for the P2X3 receptor subtype. NBP, metabolite isopentenyl pyrophosphate, and endogenous AMP did not exert any inhibitory action, indicating that only intact ApppI has inhibitory activity. Ca21-dependent inhibition was stronger in trigeminal neurons preferentially expressing desensitizing P2X3 subunits than in nodose ganglia neurons, which also express nondesensitizing P2X2 subunits. Altogether, we characterized previously unknown purinergic mechanisms of NBP-induced metabolites and suggest ApppI as the endogenous pain inhibitor contributing to cancer treatment with NBPs.

Last updated on 2019-29-01 at 21:37