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Astilbe chinensis Modulates Platelet Function via Impaired MAPK and PLCγ2 Expression

BACKGROUND: Platelets play major role in maintaining hemostasis while hyperactivation of platelets may lead to arterial thrombosis. Natural products and ethnomedicine have been shown to reduce the risk of cardiovascular diseases (CVDs). Astilbe chinensis is a perennial herb found in China, Korea, Ru...

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Autores principales: Jeon, Bo-Ra, Irfan, Muhammad, Lee, Seung Eun, Lee, Jeong Hoon, Rhee, Man Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6098923/
https://www.ncbi.nlm.nih.gov/pubmed/30174701
http://dx.doi.org/10.1155/2018/3835021
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author Jeon, Bo-Ra
Irfan, Muhammad
Lee, Seung Eun
Lee, Jeong Hoon
Rhee, Man Hee
author_facet Jeon, Bo-Ra
Irfan, Muhammad
Lee, Seung Eun
Lee, Jeong Hoon
Rhee, Man Hee
author_sort Jeon, Bo-Ra
collection PubMed
description BACKGROUND: Platelets play major role in maintaining hemostasis while hyperactivation of platelets may lead to arterial thrombosis. Natural products and ethnomedicine have been shown to reduce the risk of cardiovascular diseases (CVDs). Astilbe chinensis is a perennial herb found in China, Korea, Russia, and Japan, which is also known for its medicinal effects, and has been used in Korean traditional medicine to treat inflammation, cancer, chronic bronchitis, and headache. We hypothesized that given herbal plant exhibits pharmacological activities against CVDs, and we specifically explored their effects on platelet function. METHODOLOGY: Platelet aggregation was evaluated using standard light-transmission aggregometry. Intracellular calcium mobilization was assessed using Fura-2/AM, and granule secretion (ATP release) was measured in a luminometer. Fibrinogen binding to integrin α(IIb)β(3) was assessed using flow cytometry. Phosphorylation of mitogen-activated protein kinase (MAPK) signaling molecules and activation of the phosphoinositide 3-kinase (PI3K)/Akt were assessed using western blots, and further, glycoprotein VI (GPVI) signaling components were studied using immunoprecipitation. KEY RESULTS: A. chinensis extracts potently and significantly inhibited platelet aggregation, calcium mobilization, granule secretion, and fibrinogen binding to integrin α(IIb)β(3). Moreover, it significantly inhibited MAPK phosphorylation and expression of GPVI downstream signaling molecules. CONCLUSION: A. chinensis extract inhibited platelet aggregation and granule secretion and attenuated GPVI downstream signaling, indicating the potential therapeutic effects of this plant extract on the cardiovascular system and platelet function. We suggest that given plant extract may be a potent candidate to treat platelet-related CVDs and to be used as antiplatelet agent.
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spelling pubmed-60989232018-09-02 Astilbe chinensis Modulates Platelet Function via Impaired MAPK and PLCγ2 Expression Jeon, Bo-Ra Irfan, Muhammad Lee, Seung Eun Lee, Jeong Hoon Rhee, Man Hee Evid Based Complement Alternat Med Research Article BACKGROUND: Platelets play major role in maintaining hemostasis while hyperactivation of platelets may lead to arterial thrombosis. Natural products and ethnomedicine have been shown to reduce the risk of cardiovascular diseases (CVDs). Astilbe chinensis is a perennial herb found in China, Korea, Russia, and Japan, which is also known for its medicinal effects, and has been used in Korean traditional medicine to treat inflammation, cancer, chronic bronchitis, and headache. We hypothesized that given herbal plant exhibits pharmacological activities against CVDs, and we specifically explored their effects on platelet function. METHODOLOGY: Platelet aggregation was evaluated using standard light-transmission aggregometry. Intracellular calcium mobilization was assessed using Fura-2/AM, and granule secretion (ATP release) was measured in a luminometer. Fibrinogen binding to integrin α(IIb)β(3) was assessed using flow cytometry. Phosphorylation of mitogen-activated protein kinase (MAPK) signaling molecules and activation of the phosphoinositide 3-kinase (PI3K)/Akt were assessed using western blots, and further, glycoprotein VI (GPVI) signaling components were studied using immunoprecipitation. KEY RESULTS: A. chinensis extracts potently and significantly inhibited platelet aggregation, calcium mobilization, granule secretion, and fibrinogen binding to integrin α(IIb)β(3). Moreover, it significantly inhibited MAPK phosphorylation and expression of GPVI downstream signaling molecules. CONCLUSION: A. chinensis extract inhibited platelet aggregation and granule secretion and attenuated GPVI downstream signaling, indicating the potential therapeutic effects of this plant extract on the cardiovascular system and platelet function. We suggest that given plant extract may be a potent candidate to treat platelet-related CVDs and to be used as antiplatelet agent. Hindawi 2018-08-05 /pmc/articles/PMC6098923/ /pubmed/30174701 http://dx.doi.org/10.1155/2018/3835021 Text en Copyright © 2018 Bo-Ra Jeon et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jeon, Bo-Ra
Irfan, Muhammad
Lee, Seung Eun
Lee, Jeong Hoon
Rhee, Man Hee
Astilbe chinensis Modulates Platelet Function via Impaired MAPK and PLCγ2 Expression
title Astilbe chinensis Modulates Platelet Function via Impaired MAPK and PLCγ2 Expression
title_full Astilbe chinensis Modulates Platelet Function via Impaired MAPK and PLCγ2 Expression
title_fullStr Astilbe chinensis Modulates Platelet Function via Impaired MAPK and PLCγ2 Expression
title_full_unstemmed Astilbe chinensis Modulates Platelet Function via Impaired MAPK and PLCγ2 Expression
title_short Astilbe chinensis Modulates Platelet Function via Impaired MAPK and PLCγ2 Expression
title_sort astilbe chinensis modulates platelet function via impaired mapk and plcγ2 expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6098923/
https://www.ncbi.nlm.nih.gov/pubmed/30174701
http://dx.doi.org/10.1155/2018/3835021
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