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Antithrombotic effects and related mechanisms of Salvia deserta Schang root EtOAc extracts

Salvia deserta Schang (SDS) belongs to the same family as Salvia miltiorrhiza bunge, one of the antithrombotic Chinese herbal medicines. In our study, EtOAc root extracts were analyzed for their effects on adenosine diphosphate (ADP)-induced platelet aggregation in rabbits and FeCl(3)-induced rat co...

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Autores principales: Kasimu, Rena, Wang, Xinling, Wang, Xiaomei, Hu, Junping, Wang, Xiaoqing, Mu, Yuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288089/
https://www.ncbi.nlm.nih.gov/pubmed/30532017
http://dx.doi.org/10.1038/s41598-018-36026-7
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author Kasimu, Rena
Wang, Xinling
Wang, Xiaomei
Hu, Junping
Wang, Xiaoqing
Mu, Yuming
author_facet Kasimu, Rena
Wang, Xinling
Wang, Xiaomei
Hu, Junping
Wang, Xiaoqing
Mu, Yuming
author_sort Kasimu, Rena
collection PubMed
description Salvia deserta Schang (SDS) belongs to the same family as Salvia miltiorrhiza bunge, one of the antithrombotic Chinese herbal medicines. In our study, EtOAc root extracts were analyzed for their effects on adenosine diphosphate (ADP)-induced platelet aggregation in rabbits and FeCl(3)-induced rat common carotid artery thrombosis as well as on rat blood plasma concentrations of thromboxane B2 (TXB(2)), 6-keto-prostaglandin F1 alpha (6-keto-PGF(1α)), antithrombin-III (AT-III), protein C (PC), plasminogen (PLG), plasminogen activator inhibitor (PAI-1), von Willebrand factor (vWF) and tissue-type plasminogen activator (t-PA). EtOAc extracts from SDS roots had significant inhibitory effects on ADP-induced maximum platelet aggregation rate (10.2 ± 2.6 vs control 35.7 ± 5.2; P < 0.05), reduced the FeCl(3)-induced rat common carotid artery thrombus weight and thrombus area ratio (P < 0.05), significantly decreased plasma TXB(2), vWF and PAI-1 levels and increased 6-keto-PGF(1α) and t-PA levels in a dose dependent manner (all P < 0.05). Thus, the ratio of TXB(2)/6-keto-PGF(1α) was significantly decreased (P < 0.05), while the ratio of t-PA/PAI-1 was significantly increased (P < 0.05). In addition, enhanced AT-III and PC activities indicated coagulation inactivation effects of EtOAc SDS root extracts. EtOAc extraction from SDS showed antithrombotic effects, which are likely due to platelet adhesion and aggregation inhibition as well as anticoagulant activities.
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spelling pubmed-62880892018-12-19 Antithrombotic effects and related mechanisms of Salvia deserta Schang root EtOAc extracts Kasimu, Rena Wang, Xinling Wang, Xiaomei Hu, Junping Wang, Xiaoqing Mu, Yuming Sci Rep Article Salvia deserta Schang (SDS) belongs to the same family as Salvia miltiorrhiza bunge, one of the antithrombotic Chinese herbal medicines. In our study, EtOAc root extracts were analyzed for their effects on adenosine diphosphate (ADP)-induced platelet aggregation in rabbits and FeCl(3)-induced rat common carotid artery thrombosis as well as on rat blood plasma concentrations of thromboxane B2 (TXB(2)), 6-keto-prostaglandin F1 alpha (6-keto-PGF(1α)), antithrombin-III (AT-III), protein C (PC), plasminogen (PLG), plasminogen activator inhibitor (PAI-1), von Willebrand factor (vWF) and tissue-type plasminogen activator (t-PA). EtOAc extracts from SDS roots had significant inhibitory effects on ADP-induced maximum platelet aggregation rate (10.2 ± 2.6 vs control 35.7 ± 5.2; P < 0.05), reduced the FeCl(3)-induced rat common carotid artery thrombus weight and thrombus area ratio (P < 0.05), significantly decreased plasma TXB(2), vWF and PAI-1 levels and increased 6-keto-PGF(1α) and t-PA levels in a dose dependent manner (all P < 0.05). Thus, the ratio of TXB(2)/6-keto-PGF(1α) was significantly decreased (P < 0.05), while the ratio of t-PA/PAI-1 was significantly increased (P < 0.05). In addition, enhanced AT-III and PC activities indicated coagulation inactivation effects of EtOAc SDS root extracts. EtOAc extraction from SDS showed antithrombotic effects, which are likely due to platelet adhesion and aggregation inhibition as well as anticoagulant activities. Nature Publishing Group UK 2018-12-10 /pmc/articles/PMC6288089/ /pubmed/30532017 http://dx.doi.org/10.1038/s41598-018-36026-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kasimu, Rena
Wang, Xinling
Wang, Xiaomei
Hu, Junping
Wang, Xiaoqing
Mu, Yuming
Antithrombotic effects and related mechanisms of Salvia deserta Schang root EtOAc extracts
title Antithrombotic effects and related mechanisms of Salvia deserta Schang root EtOAc extracts
title_full Antithrombotic effects and related mechanisms of Salvia deserta Schang root EtOAc extracts
title_fullStr Antithrombotic effects and related mechanisms of Salvia deserta Schang root EtOAc extracts
title_full_unstemmed Antithrombotic effects and related mechanisms of Salvia deserta Schang root EtOAc extracts
title_short Antithrombotic effects and related mechanisms of Salvia deserta Schang root EtOAc extracts
title_sort antithrombotic effects and related mechanisms of salvia deserta schang root etoac extracts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288089/
https://www.ncbi.nlm.nih.gov/pubmed/30532017
http://dx.doi.org/10.1038/s41598-018-36026-7
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