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  <controlfield tag="001">130448</controlfield>
  <controlfield tag="005">20240125162930.0</controlfield>
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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1177/1753425909104781</subfield>
  </datafield>
  <datafield tag="024" ind1="8" ind2=" ">
    <subfield code="2">sideral</subfield>
    <subfield code="a">116144</subfield>
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  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">ART-2009-116144</subfield>
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  <datafield tag="041" ind1=" " ind2=" ">
    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Mendoza, Carmen</subfield>
  </datafield>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Lipopolysaccharide induces alteration of serotonin transporter in human intestinal epithelial cells</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2009</subfield>
  </datafield>
  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Intestinal serotoninergic activity and serotonin transporter (SERT) function have been shown to be altered in intestinal inflammatory diseases. Serotonin (5-HT) plays a critical role in the regulation of gastrointestinal physiology. Activity of 5-HT depends on its extracellular availability, partly modulated by SERT that transports 5-HT into the cell. Lipopolysaccharide (LPS) is a component of Gram-negative bacteria outer membrane, which acts as a potent activator of the inflammatory system in the intestine. The aim of this work was to determine, in the enterocyte-like cell line Caco-2, whether LPS treatment affects serotoninergic activity by acting on SERT. The results demonstrate that LPS treatment diminishes SERT activity in a dose- and period-dependent way. The kinetic study shows that V&lt;inf>max&lt;/inf> was significantly reduced after treatment with LPS. The LPS effect on 5-HT uptake was, in part, mediated by protein kinase C (PKC) activation. The molecular expression of SERT revealed that LPS treatment did not affect the mRNA level or the SERT protein content in cell homogenate. The level of SERT protein, however, was reduced on brush border membrane. The LPS effect might be due to an alteration of the intracellular traffic of SERT which may, in part, be mediated by PKC activity. ¬© SAGE Publications 2009.</subfield>
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    <subfield code="9">info:eu-repo/semantics/closedAccess</subfield>
    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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  <datafield tag="590" ind1=" " ind2=" ">
    <subfield code="a">2.206</subfield>
    <subfield code="b">2009</subfield>
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    <subfield code="a">MEDICINE, RESEARCH &amp; EXPERIMENTAL</subfield>
    <subfield code="b">41 / 91 = 0.451</subfield>
    <subfield code="c">2009</subfield>
    <subfield code="d">Q2</subfield>
    <subfield code="e">T2</subfield>
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  <datafield tag="591" ind1=" " ind2=" ">
    <subfield code="a">MICROBIOLOGY</subfield>
    <subfield code="b">54 / 95 = 0.568</subfield>
    <subfield code="c">2009</subfield>
    <subfield code="d">Q3</subfield>
    <subfield code="e">T2</subfield>
  </datafield>
  <datafield tag="591" ind1=" " ind2=" ">
    <subfield code="a">BIOCHEMISTRY &amp; MOLECULAR BIOLOGY</subfield>
    <subfield code="b">177 / 281 = 0.63</subfield>
    <subfield code="c">2009</subfield>
    <subfield code="d">Q3</subfield>
    <subfield code="e">T2</subfield>
  </datafield>
  <datafield tag="591" ind1=" " ind2=" ">
    <subfield code="a">IMMUNOLOGY</subfield>
    <subfield code="b">87 / 126 = 0.69</subfield>
    <subfield code="c">2009</subfield>
    <subfield code="d">Q3</subfield>
    <subfield code="e">T3</subfield>
  </datafield>
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    <subfield code="a">info:eu-repo/semantics/article</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Matheus, Nyurky</subfield>
    <subfield code="0">(orcid)0000-0002-1605-0542</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Iceta, Ruth</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Mesonero, Jose E.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-4758-3998</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Alcalde, Ana I.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-9935-927X</subfield>
  </datafield>
  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1005</subfield>
    <subfield code="2">410</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Farmacología y Fisiolog.</subfield>
    <subfield code="c">Área Fisiología</subfield>
  </datafield>
  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">15, 4 (2009), 243-250</subfield>
    <subfield code="p">Innate immun.</subfield>
    <subfield code="t">Innate Immunity</subfield>
    <subfield code="x">1753-4259</subfield>
  </datafield>
  <datafield tag="856" ind1="4" ind2=" ">
    <subfield code="s">198077</subfield>
    <subfield code="u">http://zaguan.unizar.es/record/130448/files/texto_completo.pdf</subfield>
    <subfield code="y">Versión publicada</subfield>
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