Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21155
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dc.date.accessioned2021-07-07T10:35:53Z-
dc.date.available2021-07-07T10:35:53Z-
dc.date.issued2005-09-
dc.identifier.citationIlcol, Y. O. vd. (2005). "Endotoxin alters serum-free choline and phospholipid-bound choline concentrations, and choline administration attenuates endotoxin-induced organ injury in dogs". Shock, 24(3), 288-293.en_US
dc.identifier.issn1073-2322-
dc.identifier.urihttps://doi.org/10.1097/01.shk.0000174018.02688.4b-
dc.identifier.urihttps://journals.lww.com/shockjournal/Fulltext/2005/09000/ENDOTOXIN_ALTERS_SERUM_FREE_CHOLINE_AND.15.aspx-
dc.identifier.urihttp://hdl.handle.net/11452/21155-
dc.description.abstractThis study in dogs was performed to assess circulating choline status during endotoxemia and to determine whether choline administration can protect dogs from endotoxin-induced tissue injuries. Baseline serum-free and phospholipid-bound choline concentrations were 19.2 +/- 0.6 mu mol/L and 3700 +/- 70 mu mol/L, respectively. After intravenous endotoxin infusion, serum-free choline concentrations decreased by 14% to 49% (P < 0.05-0.001) at 2 to 6 h after 0.02 mg/kg endotoxin, and increased by 23% to 98% (P < 0.05-0.001) at 1 to 48 h after 1 mg/kg endotoxin. Serum phospholipid-bound choline concentrations increased by 19% to 27% (P < 0.05) at 12 to 24 h or by 18% to 53% (P < 0.05-0.001) at 1 to 48 h after 0.02 or 1 mg/kg endotoxin, respectively. The changes in serum-free and -bound choline levels in response to endotoxin were accompanied by dose- and time-related elevations in serum cortisol and biochemical markers for tissue injury and/or organ dysfunction. Intravenous administration of choline (20 mg/kg) 5 min before, and 4 and 8 h after endotoxin (11 mg/kg) attenuated endotoxin-induced elevations in serum alanine aminotransferase (P < 0.05-0.001), aspartate aminotransferase (P < 0.05-0.001), -y-glutamyl transferase (P < 0.05-0.001), alkaline phosphatase (P < 0.05-0.001), lactate dehydrogenase (P < 0.05-0.001), myocardial creatine kinase (P < 0.001), urea (P < 0.05-0.01), creatinine (P < 0.05), uric acid (P < 0.010.001), and tissue necrosis factor-alpha (P < 0.001). Choline also attenuated alanine ami notransf erase (P < 0.05-0.01), alkaline phosphatase (P < 0.05-0.01), lactate dehydrogenase (P < 0.05-0.01), creatine kinase (P < 0.05-0.001), myocardial creatine kinase (P < 0.05-0.001), and uric acid (P < 0.05-0.01), but failed to alter the serum urea, creatinine, aspartate aminotransf erase, and gamma-glutamyl transferase responses to 0.02 mg/kg endotoxin. These data show that choline status is altered during endotoxemia and that choline administration diminishes endotoxin-induced tissue injury.en_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectLipopolysaccharideen_US
dc.subjectLiver injuryen_US
dc.subjectCholine statusen_US
dc.subjectEndotoxemiaen_US
dc.subjectTissue injuryen_US
dc.subjectPlasma-freeen_US
dc.subjectLysophosphatidylcholineen_US
dc.subjectSepsisen_US
dc.subjectSurgeryen_US
dc.subjectShocken_US
dc.subjectRaten_US
dc.subjectIncreasesen_US
dc.subjectDecreaseen_US
dc.subjectHumansen_US
dc.subjectHemodialysisen_US
dc.subjectGeneral & internal medicineen_US
dc.subjectCardiovascular system & cardiologyen_US
dc.subjectHematologyen_US
dc.subjectSurgeryen_US
dc.titleEndotoxin alters serum-free choline and phospholipid-bound choline concentrations, and choline administration attenuates endotoxin-induced organ injury in dogsen_US
dc.typeArticleen_US
dc.identifier.wos000231752300015tr_TR
dc.identifier.scopus2-s2.0-24644514247tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Dahiliye Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Farmakoloji ve Klinik Farmakoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyokimya ve Klinik Biyokimya Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0001-9836-0749tr_TR
dc.identifier.startpage288tr_TR
dc.identifier.endpage293tr_TR
dc.identifier.volume24tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalShocktr_TR
dc.contributor.buuauthorIlçol, Yeşim Özarda-
dc.contributor.buuauthorYılmaz, Zeki-
dc.contributor.buuauthorUlus, İsmail Hakki-
dc.contributor.researcheridA-9637-2008tr_TR
dc.contributor.researcheridD-5340-2015tr_TR
dc.contributor.researcheridAAL-8873-2021tr_TR
dc.identifier.pubmed16135970tr_TR
dc.subject.wosCritical care medicineen_US
dc.subject.wosPeripheral vascular diseaseen_US
dc.subject.wosHematologyen_US
dc.subject.wosSurgeryen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ1 (Critical care medicine)en_US
dc.wos.quartileQ1 (Surgery)en_US
dc.wos.quartileQ2en_US
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