TY - JOUR
T1 - Hinokitiol inhibits platelet activation ex vivo and thrombus formation in vivo
AU - Lin, Kuan H.
AU - Kuo, Jinn R.
AU - Lu, Wan-Jung
AU - Chung, Chi L.
AU - Chou, Duen S.
AU - Huang, Shih Y.
AU - Lee, Hsiu C.
AU - Sheu, Joen R.
N1 - Funding Information:
This work was supported by grants from the National Science Council , Taiwan ( NSC100-2320-B-038-021-MY3 , NSC101-2811-B-038-002 , and NSC101-2811-B-038-006 ); Chi-Mei Medical Center-Taipei Medical University ( 100CM-TMU-02 ); and Shin Kong Wu Ho-Su Memorial Hospital ( SKH-8302-101-NDR-09 and SKH-8302-102-NDR-04 ).
PY - 2013/5/15
Y1 - 2013/5/15
N2 - Hinokitiol is a tropolone-related bioactive compound that has been used in hair tonics, cosmetics, and food as an antimicrobial agent. Recently, hinokitiol has attracted considerable interest because of its anticancer activities. Platelet activation plays a crucial role in atherothrombotic processes. We examined the effects of hinokitiol treatment on platelet activation using human platelets. In the present study, hinokitiol (1 and 2 μM) inhibited the collagen-induced aggregation of human platelets, but did not inhibit the activation of platelets by other agonists, including thrombin, arachidonic acid, and ADP. Hinokitiol inhibited the phosphorylation of phospholipase C (PLC)γ2, protein kinase C (PKC), mitogen-activated protein kinases (MAPKs), and Akt in collagen-activated human platelets, and significantly reduced intracellular calcium mobilization and hydroxyl radical (OH) formation. Hinokitiol also reduced the PKC activation and platelet aggregation stimulated by PDBu. In addition, hinokitiol significantly prolonged thrombogenesis in mice. Hinokitiol did not influence the binding of a fluorescent triflavin probe to the αIIbβ3 integrin on platelet membrane, and neither ODQ nor SQ22536 significantly reversed the hinokitiol-mediated inhibition of platelet aggregation. In conclusion, hinokitiol may inhibit platelet activation by inhibiting the PLCγ2-PKC cascade and hydroxyl radical formation, followed by suppressing the activation of MAPKs and Akt. Our study suggests that hinokitiol may represent a potential therapeutic agent for the prevention or treatment of thromboembolic disorders. AbbreviationsBSAbovine serum albumincPLA2cytosolic phospholipase A 2CVDscardiovascular diseasesDAGdiacylglycerolDTSthe dense tubular systemERKextracellular signal-regulated kinaseESRelectron spin resonanceHOhydroxyl radicalIP3inositol 1,4,5-trisphosphateJNKc-Jun N-terminal kinaseNTGnitroglycerinPGE1prostaglandin E 1PKCprotein kinase CPRPplatelet-rich plasmaTxA2thromboxane A2.
AB - Hinokitiol is a tropolone-related bioactive compound that has been used in hair tonics, cosmetics, and food as an antimicrobial agent. Recently, hinokitiol has attracted considerable interest because of its anticancer activities. Platelet activation plays a crucial role in atherothrombotic processes. We examined the effects of hinokitiol treatment on platelet activation using human platelets. In the present study, hinokitiol (1 and 2 μM) inhibited the collagen-induced aggregation of human platelets, but did not inhibit the activation of platelets by other agonists, including thrombin, arachidonic acid, and ADP. Hinokitiol inhibited the phosphorylation of phospholipase C (PLC)γ2, protein kinase C (PKC), mitogen-activated protein kinases (MAPKs), and Akt in collagen-activated human platelets, and significantly reduced intracellular calcium mobilization and hydroxyl radical (OH) formation. Hinokitiol also reduced the PKC activation and platelet aggregation stimulated by PDBu. In addition, hinokitiol significantly prolonged thrombogenesis in mice. Hinokitiol did not influence the binding of a fluorescent triflavin probe to the αIIbβ3 integrin on platelet membrane, and neither ODQ nor SQ22536 significantly reversed the hinokitiol-mediated inhibition of platelet aggregation. In conclusion, hinokitiol may inhibit platelet activation by inhibiting the PLCγ2-PKC cascade and hydroxyl radical formation, followed by suppressing the activation of MAPKs and Akt. Our study suggests that hinokitiol may represent a potential therapeutic agent for the prevention or treatment of thromboembolic disorders. AbbreviationsBSAbovine serum albumincPLA2cytosolic phospholipase A 2CVDscardiovascular diseasesDAGdiacylglycerolDTSthe dense tubular systemERKextracellular signal-regulated kinaseESRelectron spin resonanceHOhydroxyl radicalIP3inositol 1,4,5-trisphosphateJNKc-Jun N-terminal kinaseNTGnitroglycerinPGE1prostaglandin E 1PKCprotein kinase CPRPplatelet-rich plasmaTxA2thromboxane A2.
KW - Hinokitiol
KW - Hydroxyl radical
KW - MAPK
KW - Occlusion time
KW - PLCγ2
KW - Platelet activation
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U2 - 10.1016/j.bcp.2013.02.027
DO - 10.1016/j.bcp.2013.02.027
M3 - Article
C2 - 23473801
AN - SCOPUS:84876681795
SN - 0006-2952
VL - 85
SP - 1478
EP - 1485
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 10
ER -