﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Shahrekord University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Herbmed Pharmacology</JournalTitle>
      <Issn>2345-5004</Issn>
      <Volume>10</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2021</Year>
        <Month>07</Month>
        <DAY>03</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Macrostachyols A-D, oligostilbenes from Gnetum macrostachyum inhibited in vitro human platelet aggregation</ArticleTitle>
    <FirstPage>339</FirstPage>
    <LastPage>343</LastPage>
    <ELocationID EIdType="doi">10.34172/jhp.2021.39</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Serm</FirstName>
        <LastName>Surapinit</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-6723-9751</Identifier>
      </Author>
      <Author>
        <FirstName>Nuttakorn</FirstName>
        <LastName>Baisaeng</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-0305-5854</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/jhp.2021.39</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>02</Month>
        <Day>09</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>03</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Gnetum macrostachyum is a known Thai medicinal plant as a source of bioactive oligostilbenes, which possess platelet inhibitory activities. The study aimed to evaluate the in vitro human platelet aggregation inhibitory activities of macrostachyols A-D (compounds 1-4) isolated from the roots of G. macrostachyum. Methods: The in vitro human platelet aggregation assay was assayed with a 96-well microtiter plate format. The well-known aggregating agents were used to investigate the possible mechanism of inhibition, including adenosine diphosphate (ADP), arachidonic acid (AA), thromboxane A2 analog (U-46619), collagen, thrombin, and thrombin receptor-activating peptide-6 (TRAP-6). Results: Compound 1 was more potent than ibuprofen (positive control) on the adenosine diphosphate- induced platelet aggregation assay (P &lt; 0.05). Compound 3 was more potent than 1, 2, and 4 (P &lt; 0.05), but all active oligostilbenes were less potent than the positive control (P &lt; 0.05) on the arachidonic acid-induced platelet aggregation assay. The oligostilbenes 1, 2, 3, and 4 also displayed the inhibitory effects on the U-46619-induced platelet aggregation. The tetrameric stilbenes 1 was the only compound that exhibited inhibitory effects on thrombin-induced platelet aggregation without TRAP-6 mediated platelet aggregation. Conclusion: The findings revealed the inhibitory effects of oligostilbenes on human platelet aggregation through a target-specific experimental design. It suggests that oligostilbenes from this plant might be applied as antiplatelet aggregation agents in platelet hyperreactivity- related diseases.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Gnetum</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Stilbenes</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Platelet Aggregation Inhibitors</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Cyclooxygenase Inhibitors</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Oligostilbenes</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>