Inhibition of aggregation of rabbit and human platelets induced by adrenaline and 5-hydroxytryptamine by KB-R7943, a Na+/Ca2+ exchange inhibitor

Citation
S. Takano et al., Inhibition of aggregation of rabbit and human platelets induced by adrenaline and 5-hydroxytryptamine by KB-R7943, a Na+/Ca2+ exchange inhibitor, BR J PHARM, 132(7), 2001, pp. 1383-1388
Citations number
22
Categorie Soggetti
Pharmacology & Toxicology
Journal title
BRITISH JOURNAL OF PHARMACOLOGY
ISSN journal
00071188 → ACNP
Volume
132
Issue
7
Year of publication
2001
Pages
1383 - 1388
Database
ISI
SICI code
0007-1188(200104)132:7<1383:IOAORA>2.0.ZU;2-P
Abstract
1 We investigated the effect of KB-R7943, a Na+/Ca2+ exchange inhibitor, on the aggregation response induced by adrenaline and 5-hydroxytryptamine (5- HT), alone or in combination in human and rabbit platelets in the presence or absence of ouabain. 2 KB-R7943 inhibited aggregation induced by the combination of adrenaline a nd 5-HT in a concentration-dependent manner. The ICS, values of KB-R7943 we re 4.2 +/-2.0 or 3.0 +/-0.7 muM with washed rabbit platelets with or withou t ouabain pretreatment, respectively. 3 In platelet-rich human plasma, the aggregation was biphasic. The IC50 val ue of KB-R7943 was 17.2 +/-4.4 muM for the first phase aggregation. 4 KB-R7943 did not inhibit the first phase of aggregation induced by adrena line alone, or the monophasic aggregation induced by 5-HT alone. 5 The aggregation of rabbit platelets depended on the presence of K+ in the medium, and K+-dependent and K+-independent Ca2+ influx were observed in r esting platelets. Ouabain treatment increased only the Ki-dependent but not the K+-independent Ca2+ influx. 6 KB-R7943 inhibited K+-dependent Ca2+ influx with or without ouabain pretr eatment, but not K+-independent Ca2+ influx. 7 From these results, we conclude that KB-R7943 inhibits the adrenaline plu s 5-HT induced aggregation of rabbit and human platelets by inhibiting K+-d ependent Na+/Ca2+ (NCKX). Our results suggest that NCKX plays an important role in platelet aggregation.