
Platelet inhibitory effects of the Phase 3 anticancer and normal tissue cytoprotective agent, RR x‐001
Author(s) -
Oronsky Bryan,
Oronsky Neil,
Cabrales Pedro
Publication year - 2018
Publication title -
journal of cellular and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.44
H-Index - 130
eISSN - 1582-4934
pISSN - 1582-1838
DOI - 10.1111/jcmm.13791
Subject(s) - nitric oxide , platelet , chemistry , pharmacology , nitrite , biochemistry , ex vivo , platelet activation , immunology , in vitro , medicine , organic chemistry , nitrate
The platelet inhibitory effects of the Phase 3 anticancer agent and nitric oxide ( NO ) donor, RR x‐001, (1‐bromoacetyl‐3,3‐dinitroazetidine) were examined ex vivo and compared with the diazeniumdiolate NO donor, diethylenetriamine NONO ate ( DETA ‐ NONO ate), which spontaneously releases nitric oxide in aqueous solution. In the absence of red blood cells and in a dose‐dependent manner, DETA ‐ NONO ate strongly inhibited platelet aggregation induced by several stimuli ( ADP , epinephrine and collagen) whereas RR x‐001 only slightly inhibited platelet aggregation under the same conditions in a dose‐dependent manner; these antiaggregant effects were blocked when both DETA ‐ NONO ate and RR x‐001 were co‐incubated with carboxy‐ PTIO ( CPTIO 0.01‐100 micromol), a widely accepted NO scavenger. However, in the presence of red blood cells from healthy human donors, RR x‐001, which binds covalently to haemoglobin (Hb) and catalyses the production of NO from endogenous nitrite, more strongly inhibited the aggregation of platelets than DETA ‐ NONO ate in a dose‐dependent manner likely because haemoglobin avidly scavenges nitric oxide and reduces its half‐life; the RR x‐001‐mediated platelet inhibitory effect was increased in the presence of nitrite. The results of this study suggest that RR x‐001‐bound Hb (within RBC s) plays an important role in the bioconversion of NO 2 − to NO . , which makes RR x‐001 a more physiologically relevant inhibitor of platelet aggregation than other nitric oxide donors, whose effects are attenuated in the presence of red blood cells. Therefore, RR x‐001‐mediated platelet inhibition is a potentially useful therapeutic property, especially in hypercoagulable cancer patients that are at an increased risk of thrombotic complications.