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Antiplatelet activity of J78 (2-chloro-3-[2′-bromo, 4′-fluoro-phenyl]-amino-8-hydroxy-1,4-naphthoquinone), an antithrombotic agent, is mediated by thromboxane (TX) A2 receptor blockade with TXA2 synthase inhibition and suppression of cytosolic Ca2+ mobilization

Title
Antiplatelet activity of J78 (2-chloro-3-[2′-bromo, 4′-fluoro-phenyl]-amino-8-hydroxy-1,4-naphthoquinone), an antithrombotic agent, is mediated by thromboxane (TX) A2 receptor blockade with TXA2 synthase inhibition and suppression of cytosolic Ca2+ mobilization
Authors
Jin Y.-R.Cho M.-R.Ryu C.-K.Chung J.-H.Yuk D.-Y.Hong J.-T.Lee K.-S.Lee J.-J.Lee M.-Y.Lim Y.Yun Y.-P.
Ewha Authors
유충규
SCOPUS Author ID
유충규scopus
Issue Date
2005
Journal Title
Journal of Pharmacology and Experimental Therapeutics
ISSN
0022-3565JCR Link
Citation
vol. 312, no. 1, pp. 214 - 219
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
We previously reported that J78 (2-chloro-3-[2′-bromo, 4′-fluoro-phenyl]-amino-8-hydroxy-1,4-naphthoquinone), a newly synthesized 1,4-naphthoquinone derivative, exhibited a potent antithrombotic effect, which might be due to antiplatelet rather than anticoagulation activity. In the present study, possible anti-platelet mechanism of J78 was investigated. J78 concentration-dependently inhibited rabbit platelet aggregation induced by collagen (10 μg/ml), thrombin (0.05 U/ml), arachidonic acid (100 μM), and U46619 (9,11-dideoxy-9,11-methanoepoxy-prostaglandin F2; 1 μM), a thromboxane (TX) A2 mimic, with IC50 values of 0.32 ± 0.01, 0.44 ± 0.02, 0.50 ± 0.04, and 0.36 ± 0.02 μM, respectively. J78 also produced a shift to the right of the concentration-response curve of U46619, indicating an antagonistic effect on the TXA2 receptor. J78 concentration-dependently inhibited collagen-induced arachidonic acid liberation. In addition, J78 potently suppressed TXA2 formation by platelets that were exposed to arachidonic acid in a concentration-dependent manner but had no effect on the production of PGD2, indicating an inhibitory effect on TXA 2 synthase. This was supported by a TXA2 synthase activity assay that J78 concentration-dependently inhibited TXB2 formation converted from PGH2. Furthermore, J78 was also able to inhibit the [Ca2+]i mobilization induced by collagen or thrombin at such a concentration that completely inhibited platelet aggregation. Taken together, these results suggest that the antiplatelet activity of J78 may be mediated by TXA2 receptor blockade with TXA2 synthase inhibition and suppression of cytosolic Ca2+ mobilization.
DOI
10.1124/jpet.104.073718
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약학대학 > 약학과 > Journal papers
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