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DC Field | Value | Language |
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dc.date.accessioned | 2021-07-07T10:35:53Z | - |
dc.date.available | 2021-07-07T10:35:53Z | - |
dc.date.issued | 2005-09 | - |
dc.identifier.citation | Ilcol, 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.issn | 1073-2322 | - |
dc.identifier.uri | https://doi.org/10.1097/01.shk.0000174018.02688.4b | - |
dc.identifier.uri | https://journals.lww.com/shockjournal/Fulltext/2005/09000/ENDOTOXIN_ALTERS_SERUM_FREE_CHOLINE_AND.15.aspx | - |
dc.identifier.uri | http://hdl.handle.net/11452/21155 | - |
dc.description.abstract | This 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.iso | en | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Lipopolysaccharide | en_US |
dc.subject | Liver injury | en_US |
dc.subject | Choline status | en_US |
dc.subject | Endotoxemia | en_US |
dc.subject | Tissue injury | en_US |
dc.subject | Plasma-free | en_US |
dc.subject | Lysophosphatidylcholine | en_US |
dc.subject | Sepsis | en_US |
dc.subject | Surgery | en_US |
dc.subject | Shock | en_US |
dc.subject | Rat | en_US |
dc.subject | Increases | en_US |
dc.subject | Decrease | en_US |
dc.subject | Humans | en_US |
dc.subject | Hemodialysis | en_US |
dc.subject | General & internal medicine | en_US |
dc.subject | Cardiovascular system & cardiology | en_US |
dc.subject | Hematology | en_US |
dc.subject | Surgery | en_US |
dc.title | Endotoxin alters serum-free choline and phospholipid-bound choline concentrations, and choline administration attenuates endotoxin-induced organ injury in dogs | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000231752300015 | tr_TR |
dc.identifier.scopus | 2-s2.0-24644514247 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Dahiliye Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Farmakoloji ve Klinik Farmakoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Biyokimya ve Klinik Biyokimya Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0001-9836-0749 | tr_TR |
dc.identifier.startpage | 288 | tr_TR |
dc.identifier.endpage | 293 | tr_TR |
dc.identifier.volume | 24 | tr_TR |
dc.identifier.issue | 3 | tr_TR |
dc.relation.journal | Shock | tr_TR |
dc.contributor.buuauthor | Ilçol, Yeşim Özarda | - |
dc.contributor.buuauthor | Yılmaz, Zeki | - |
dc.contributor.buuauthor | Ulus, İsmail Hakki | - |
dc.contributor.researcherid | A-9637-2008 | tr_TR |
dc.contributor.researcherid | D-5340-2015 | tr_TR |
dc.contributor.researcherid | AAL-8873-2021 | tr_TR |
dc.identifier.pubmed | 16135970 | tr_TR |
dc.subject.wos | Critical care medicine | en_US |
dc.subject.wos | Peripheral vascular disease | en_US |
dc.subject.wos | Hematology | en_US |
dc.subject.wos | Surgery | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | Pubmed | en_US |
dc.wos.quartile | Q1 (Critical care medicine) | en_US |
dc.wos.quartile | Q1 (Surgery) | en_US |
dc.wos.quartile | Q2 | en_US |
Appears in Collections: | Web of Science |
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