Publication:
Thromboelastographic evaluation of the effectiveness of choline or cdp-choline treatment on endotoxin-induced hemostatic alterations in dogs

dc.contributor.authorInan, Oya Eralp
dc.contributor.authorUlus, Ismail Hakki
dc.contributor.authorÖzarda, Yesim
dc.contributor.buuauthorKOCATÜRK, MERİÇ
dc.contributor.buuauthorCANSEV, MEHMET
dc.contributor.buuauthorYILMAZ, ZEKİ
dc.contributor.departmentVeteriner Fakültesi
dc.contributor.departmentİç Hastalıkları Ana Bilim Dalı.
dc.contributor.departmentFarmakoloji Ana Bilim Dalı.
dc.contributor.researcheridV-5578-2017
dc.contributor.researcheridM-9071-2019
dc.date.accessioned2025-02-14T07:42:22Z
dc.date.available2025-02-14T07:42:22Z
dc.date.issued2024-03-13
dc.description.abstractSepsis/endotoxemia associates with coagulation abnormalities. We showed previously that exogenous choline treatment reversed the changes in platelet count and function as well as prevented disseminated intravascular coagulation (DIC) in endotoxemic dogs. The aim of this follow-up study was to evaluate the effect of treatment with choline or cytidine-5 ' -diphosphocholine (CDP-choline), a choline donor, on endotoxin-induced hemostatic alterations using thromboelastography (TEG). Dogs were randomized to six groups and received intravenously (iv) saline, choline (20 mg/kg) or CDP-choline (70 mg/kg) in the control groups, whereas endotoxin (0.1 mg/kg, iv) was used alone or in combination with choline or CDP-choline at the same doses in the treatment groups. TEG variables including R- and K -time (clot formation), maximum amplitude (MA) and alpha-angle (clot stability), G value (clot elasticity), and EPL, A, and LY30 (fibrinolysis), as well as overall assessment of coagulation (coagulation index - CI), were measured before and at 0.5 -48 h after the treatments. TEG parameters did not change significantly in the control groups, except for CI parameter after choline administration. Endotoxemia resulted in increased R -time and A value ( P < 0.05), decreased K -time (P < 0.05), alpha-angle ( P < 0.001) and CI values ( P < 0.01) at different time points. Treatment with either choline or CDP-choline attenuated or prevented completely the alterations in TEG parameters in endotoxemic dogs with CDP-choline being more effective. These results confirm and extend the effectiveness of choline or CDP-choline in endotoxemia by further demonstrating their efficacy in attenuating or preventing the altered viscoelastic properties of blood clot measured by TEG.
dc.description.sponsorshipTurkish Academy of Sciences (TUBA)
dc.identifier.doi10.1016/j.rvsc.2024.105205
dc.identifier.issn0034-5288
dc.identifier.scopus2-s2.0-85187575409
dc.identifier.urihttps://doi.org/10.1016/j.rvsc.2024.105205
dc.identifier.urihttps://hdl.handle.net/11452/50407
dc.identifier.volume171
dc.identifier.wos001222500800001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherElsevier Sci Ltd
dc.relation.journalResearch In Veterinary Science
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.relation.tubitak109O660
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPlatelet closure times
dc.subjectActivated thromboelastography
dc.subjectAcetylcholine synthesis
dc.subjectTyrosine-hydroxylase
dc.subjectVagus nerve
dc.subjectWhole-blood
dc.subjectRelease
dc.subjectRat
dc.subjectInvolvement
dc.subjectParameters
dc.subjectThromboelastography
dc.subjectSepsis
dc.subjectEndotoxemia
dc.subjectHemostasis
dc.subjectCoagulation
dc.subjectCholine
dc.subjectDogs
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectVeterinary sciences
dc.titleThromboelastographic evaluation of the effectiveness of choline or cdp-choline treatment on endotoxin-induced hemostatic alterations in dogs
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentVeteriner Fakültesi/İç Hastalıkları Ana Bilim Dalı.
local.contributor.departmentVeteriner Fakültesi/Farmakoloji Ana Bilim Dalı.
local.indexed.atWOS
local.indexed.atScopus
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relation.isAuthorOfPublication162b5961-162a-4862-89cd-97b30e2a2552
relation.isAuthorOfPublicationf5c45ca8-95ff-4f54-8b7d-67fa0acfe53f
relation.isAuthorOfPublication.latestForDiscoverye5873878-33c6-4ae4-89e6-5c1c62fd4768

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