Novel Therapeutic Agent against Platelet Activation In Vitro and Arterial Thrombosis In Vivo by Morin Hydrate

Morin hydrate, a bioactive flavonoid, has been proven to prevent inflammation and apoptosis of cells. Flavonoids can reduce the risk of cardiovascular diseases, in which platelet activation plays a major role. This study investigated the effect of morin hydrate on platelet activation in vitro and in...

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Main Authors: Chih-Wei Hsia, Ming-Ping Wu, Marappan Velusamy, Chih-Hsuan Hsia, Duen-Suey Chou, Cheng-Lin Tsai, Chia-Yuan Hsu, Thanasekaran Jayakumar, Chi-Li Chung, Joen-Rong Sheu
Format: Article
Language:English
Published: MDPI AG 2018-08-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/19/8/2386
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spelling doaj-cfacabfe35fc43d9beeb3d205628b06b2020-11-25T02:28:09ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-08-01198238610.3390/ijms19082386ijms19082386Novel Therapeutic Agent against Platelet Activation In Vitro and Arterial Thrombosis In Vivo by Morin HydrateChih-Wei Hsia0Ming-Ping Wu1Marappan Velusamy2Chih-Hsuan Hsia3Duen-Suey Chou4Cheng-Lin Tsai5Chia-Yuan Hsu6Thanasekaran Jayakumar7Chi-Li Chung8Joen-Rong Sheu9Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei 110, TaiwanGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei 110, TaiwanDepartment of Chemistry, North Eastern Hill University, Shillong 793022, IndiaGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei 110, TaiwanDepartment of Pharmacology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, TaiwanGraduate Institute of Metabolism and Obesity Sciences, College of Nutrition, Taipei Medical University, Taipei 110, TaiwanGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei 110, TaiwanGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei 110, TaiwanDivision of Pulmonary Medicine, Department of Internal Medical, Taipei Medical University Hospital, Taipei 110, TaiwanGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei 110, TaiwanMorin hydrate, a bioactive flavonoid, has been proven to prevent inflammation and apoptosis of cells. Flavonoids can reduce the risk of cardiovascular diseases, in which platelet activation plays a major role. This study investigated the effect of morin hydrate on platelet activation in vitro and in vivo. Morin hydrate markedly inhibited platelet aggregation stimulated by collagen in human platelets but not that stimulated by other agonists. In collagen-activated platelets, morin hydrate inhibited adenosine triphosphate (ATP) release; intracellular Ca2+ mobilization; P-selectin expression; and phosphorylation of phospholipase Cγ2 (PLCγ2), protein kinase C (PKC), and Akt. In mitogen-activated protein kinase (MAPK) activation, morin hydrate evidently diminished ERK2 or JNK1 activation, except for p38 MAPK. Additionally, morin hydrate markedly reduced the OH· signals in platelet suspensions but not in the cell-free system (Fenton reaction solution). Moreover, morin hydrate substantially increased the occlusion time of thrombotic platelet plug formation but had no effect on bleeding time in mice. In conclusion, morin hydrate crucially inhibits platelet activation through inhibition of the PLCγ2–PKC cascade and subsequent suppression of Akt and MAPK activation, thereby ultimately inhibiting platelet aggregation. Therefore, this paper suggests that morin hydrate constitutes a novel and potential natural therapeutic product for preventing or treating thromboembolic disorders.http://www.mdpi.com/1422-0067/19/8/2386bleeding timeflavonoidmorin hydrateOH· free radicalplatelet activationprotein kinasethromboembolism
collection DOAJ
language English
format Article
sources DOAJ
author Chih-Wei Hsia
Ming-Ping Wu
Marappan Velusamy
Chih-Hsuan Hsia
Duen-Suey Chou
Cheng-Lin Tsai
Chia-Yuan Hsu
Thanasekaran Jayakumar
Chi-Li Chung
Joen-Rong Sheu
spellingShingle Chih-Wei Hsia
Ming-Ping Wu
Marappan Velusamy
Chih-Hsuan Hsia
Duen-Suey Chou
Cheng-Lin Tsai
Chia-Yuan Hsu
Thanasekaran Jayakumar
Chi-Li Chung
Joen-Rong Sheu
Novel Therapeutic Agent against Platelet Activation In Vitro and Arterial Thrombosis In Vivo by Morin Hydrate
International Journal of Molecular Sciences
bleeding time
flavonoid
morin hydrate
OH· free radical
platelet activation
protein kinase
thromboembolism
author_facet Chih-Wei Hsia
Ming-Ping Wu
Marappan Velusamy
Chih-Hsuan Hsia
Duen-Suey Chou
Cheng-Lin Tsai
Chia-Yuan Hsu
Thanasekaran Jayakumar
Chi-Li Chung
Joen-Rong Sheu
author_sort Chih-Wei Hsia
title Novel Therapeutic Agent against Platelet Activation In Vitro and Arterial Thrombosis In Vivo by Morin Hydrate
title_short Novel Therapeutic Agent against Platelet Activation In Vitro and Arterial Thrombosis In Vivo by Morin Hydrate
title_full Novel Therapeutic Agent against Platelet Activation In Vitro and Arterial Thrombosis In Vivo by Morin Hydrate
title_fullStr Novel Therapeutic Agent against Platelet Activation In Vitro and Arterial Thrombosis In Vivo by Morin Hydrate
title_full_unstemmed Novel Therapeutic Agent against Platelet Activation In Vitro and Arterial Thrombosis In Vivo by Morin Hydrate
title_sort novel therapeutic agent against platelet activation in vitro and arterial thrombosis in vivo by morin hydrate
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2018-08-01
description Morin hydrate, a bioactive flavonoid, has been proven to prevent inflammation and apoptosis of cells. Flavonoids can reduce the risk of cardiovascular diseases, in which platelet activation plays a major role. This study investigated the effect of morin hydrate on platelet activation in vitro and in vivo. Morin hydrate markedly inhibited platelet aggregation stimulated by collagen in human platelets but not that stimulated by other agonists. In collagen-activated platelets, morin hydrate inhibited adenosine triphosphate (ATP) release; intracellular Ca2+ mobilization; P-selectin expression; and phosphorylation of phospholipase Cγ2 (PLCγ2), protein kinase C (PKC), and Akt. In mitogen-activated protein kinase (MAPK) activation, morin hydrate evidently diminished ERK2 or JNK1 activation, except for p38 MAPK. Additionally, morin hydrate markedly reduced the OH· signals in platelet suspensions but not in the cell-free system (Fenton reaction solution). Moreover, morin hydrate substantially increased the occlusion time of thrombotic platelet plug formation but had no effect on bleeding time in mice. In conclusion, morin hydrate crucially inhibits platelet activation through inhibition of the PLCγ2–PKC cascade and subsequent suppression of Akt and MAPK activation, thereby ultimately inhibiting platelet aggregation. Therefore, this paper suggests that morin hydrate constitutes a novel and potential natural therapeutic product for preventing or treating thromboembolic disorders.
topic bleeding time
flavonoid
morin hydrate
OH· free radical
platelet activation
protein kinase
thromboembolism
url http://www.mdpi.com/1422-0067/19/8/2386
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