1 Ocak 2014 Dergi makalesi Açık Erişim

Altinbas, Burcin; Topuz, Bora Burak; Ilhan, Tuncay; Yilmaz, Mustafa Sertac; Erdost, Hatice; Yalcin, Murat

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/63847</identifier>
  <creators>
    <creator>
      <creatorName>Altinbas, Burcin</creatorName>
      <givenName>Burcin</givenName>
      <familyName>Altinbas</familyName>
      <affiliation>Uludag Univ, Fac Vet Med, Dept Physiol, TR-16059 Bursa, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Topuz, Bora Burak</creatorName>
      <givenName>Bora Burak</givenName>
      <familyName>Topuz</familyName>
      <affiliation>Uludag Univ, Fac Vet Med, Dept Physiol, TR-16059 Bursa, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Ilhan, Tuncay</creatorName>
      <givenName>Tuncay</givenName>
      <familyName>Ilhan</familyName>
      <affiliation>Uludag Univ, Fac Vet Med, Dept Histol &amp; Embryol, TR-16059 Bursa, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Yilmaz, Mustafa Sertac</creatorName>
      <givenName>Mustafa Sertac</givenName>
      <familyName>Yilmaz</familyName>
      <affiliation>Uludag Univ, Fac Med, Dept Med Pharmacol, TR-16059 Bursa, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Erdost, Hatice</creatorName>
      <givenName>Hatice</givenName>
      <familyName>Erdost</familyName>
      <affiliation>Uludag Univ, Fac Vet Med, Dept Histol &amp; Embryol, TR-16059 Bursa, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Yalcin, Murat</creatorName>
      <givenName>Murat</givenName>
      <familyName>Yalcin</familyName>
    </creator>
  </creators>
  <titles>
    <title>Activation Of The Central Histaminergic System Mediates Arachidonic-Acid-Induced Cardiovascular Effects</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2014</publicationYear>
  <dates>
    <date dateType="Issued">2014-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/63847</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1139/cjpp-2014-0043</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">The aim of this study was to explain the involvement of the central histaminergic system in arachidonic acid (AA)-induced cardiovascular effects in normotensive rats using hemodynamic, immunohistochemistry, and microdialysis studies. Intracerebroventricularly (i.c.v.) administered AA (0.25, 0.5, and 1.0 mu mol) induced dose-and time-dependent increases in mean arterial pressure and decreased heart rate in conscious normotensive Sprague-Dawley rats. Central injection of AA (0.5 mu mol) also increased posterior hypothalamic extracellular histamine levels and produced strong COX-1 but not COX-2 immunoreactivity in the posterior hypothalamus of rats. Moreover, the cardiovascular effects and COX-1 immunoreactivity in the posterior hypothalamus induced by AA (0.5 mu mol; i.c.v.) were almost completely blocked by the H2 receptor antagonist ranitidine (50 and 100 nmol; i.c.v.) and partially blocked by the H1 receptor blocker chlorpheniramine (100 nmol; i.c.v.) and the H3-H4 receptor antagonist thioperamide (50 and 100 nmol; i.c.v.). In conclusion, these results indicate that centrally administered AA induces pressor and bradycardic responses in conscious rats. Moreover, we suggest that AA may activate histaminergic neurons and increase extracellular histamine levels, particularly in the posterior hypothalamus. Acting as a neurotransmitter, histamine is potentially involved in AA-induced cardiovascular effects under normotensive conditions.</description>
  </descriptions>
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