1 Ocak 2019 Dergi makalesi Açık Erişim

Tutun, B.; Elbe, H.; Vardi, N.; Parlakpinar, H.; Polat, A.; Gunaltili, M.; Guclu, M. M.; Yasar, E. N.

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/208279</identifier>
  <creators>
    <creator>
      <creatorName>Tutun, B.</creatorName>
      <givenName>B.</givenName>
      <familyName>Tutun</familyName>
      <affiliation>Inonu Univ, Med Fac, Malatya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Elbe, H.</creatorName>
      <givenName>H.</givenName>
      <familyName>Elbe</familyName>
      <affiliation>Mugla Sitki Kocman Univ, Med Fac, Dept Histol &amp; Embryol, Mugla, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Vardi, N.</creatorName>
      <givenName>N.</givenName>
      <familyName>Vardi</familyName>
      <affiliation>Inonu Univ, Med Fac, Dept Histol &amp; Embryol, Malatya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Parlakpinar, H.</creatorName>
      <givenName>H.</givenName>
      <familyName>Parlakpinar</familyName>
      <affiliation>Inonu Univ, Med Fac, Dept Pharmacol, Malatya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Polat, A.</creatorName>
      <givenName>A.</givenName>
      <familyName>Polat</familyName>
      <affiliation>Inonu Univ, Med Fac, Physiol, Malatya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Gunaltili, M.</creatorName>
      <givenName>M.</givenName>
      <familyName>Gunaltili</familyName>
      <affiliation>Inonu Univ, Med Fac, Malatya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Guclu, M. M.</creatorName>
      <givenName>M. M.</givenName>
      <familyName>Guclu</familyName>
      <affiliation>Inonu Univ, Med Fac, Malatya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Yasar, E. N.</creatorName>
      <givenName>E. N.</givenName>
      <familyName>Yasar</familyName>
      <affiliation>Inonu Univ, Med Fac, Malatya, Turkey</affiliation>
    </creator>
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  <titles>
    <title>Dexpanthenol Reduces Diabetic Nephropathy And Renal Oxidative Stress In Rats</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2019</publicationYear>
  <dates>
    <date dateType="Issued">2019-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/208279</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1080/10520295.2018.1508746</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">Hyperglycemia increases reactive oxygen species (ROS) and the resulting oxidative stress contributes to the development of diabetic complications. Dexpanthenol (Dxp) is the biological active form of pantothenic acid. We investigated whether Dxp administration could decrease oxidative stress as a way to treat renal complications of diabetes mellitus (DM). Thirty-two male Wistar albino rats were divided into four groups: control, Dxp, DM and DM + Dxp. Experimental diabetes was induced by a single dose of streptozotocin (STZ). After administration of STZ, the DM + Dxp group was administered 500 mg/kg Dxp intraperitoneally every day for 6 weeks. At the end of the study, blood glucose levels were measured and rats were sacrificed. Kidneys were embedded in paraffin, sectioned and stained with hematoxylin and eosin, and periodic acid-Schiff. The mean malondialdehyde levels, glutathione peroxidase, superoxide dismutase and catalase activities, and total antioxidant and total oxidant status also were measured. The control group was normal in histological appearance. We observed congestion, inflammation, glomerulosclerosis, tubular desquamation, loss of villi and hydropic degeneration in tubule cells in the DM group. Indicators of oxidative stress were elevated and antioxidant activity was reduced in the DM group compared to controls. In the DM + Dxp group, oxidative stress was decreased, antioxidant activity was increased and histopathological changes were reduced compared to the DM group. We found that Dxp exhibited ameliorative effects on STZ induced diabetic nephropathy by increasing antioxidant activity.</description>
  </descriptions>
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