Preventive effect of nimesulide on ketamine induced cardiotoxicity and the useful interaction of nimesulide with ketamine

ArticleAçık Erişim

Özet

The increased production of endogenous adrenaline (ADR) with ketamine is responsible for ketamine cardiotoxicity and the short duration of anaesthesia. The aim of this study was to investigate the effect of nimesulide on ketamine cardiotoxicity, anaesthesia duration and analgesic activity. Oxidant and anti-oxidant parameters were studied in the heart tissues, while ADR, creatine kinase-MB (CK-MB) and troponin-I (TP I) levels were measured in the blood. Malondialdehide (MDA), 8-hydroxyguanine (8-OH/Gua), CK-MB, TP I, and ADR levels in the heart tissue of the ketamine group were increased and the total glutathione (tGSH) level was decreased as compared to the healthy and nimesulide groups. However, it was found that the same parameters in the ketamine-administered adrenalectomised animals were almost identical to those of the healthy animals. Nimesulide may be useful in the reduction of ketamine cardiotoxicity, providing potent analgesia and extending the duration of anaesthesia. © 2019, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/14021Resmi atıflarda kullanılan kalıcı adres
Tam Kayıt
AlanDeğerDil
dc.contributor.authorMammadov, Renad
dc.contributor.authorAkpinar, Erol
dc.contributor.authorCoskun, Resit
dc.contributor.authorSuleyman, Halis
dc.contributor.authorGul, Mehmet A.
dc.contributor.authorKuyrukluyildiz, Ufuk
dc.date.accessioned2026-10-18T20:28:49.112463599Z
dc.date.available2026-10-18T20:28:49.112463599Z
dc.date.issued2019
dc.description.abstractThe increased production of endogenous adrenaline (ADR) with ketamine is responsible for ketamine cardiotoxicity and the short duration of anaesthesia. The aim of this study was to investigate the effect of nimesulide on ketamine cardiotoxicity, anaesthesia duration and analgesic activity. Oxidant and anti-oxidant parameters were studied in the heart tissues, while ADR, creatine kinase-MB (CK-MB) and troponin-I (TP I) levels were measured in the blood. Malondialdehide (MDA), 8-hydroxyguanine (8-OH/Gua), CK-MB, TP I, and ADR levels in the heart tissue of the ketamine group were increased and the total glutathione (tGSH) level was decreased as compared to the healthy and nimesulide groups. However, it was found that the same parameters in the ketamine-administered adrenalectomised animals were almost identical to those of the healthy animals. Nimesulide may be useful in the reduction of ketamine cardiotoxicity, providing potent analgesia and extending the duration of anaesthesia. © 2019, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.
dc.identifier.endpage72
dc.identifier.issn0326-2383
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85060998233
dc.identifier.startpage63
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14021
dc.identifier.volume38
dc.language.isoen
dc.publisherColegio de Farmaceuticos de la Provincia de Buenos Aires
dc.relation.ispartofLatin American Journal of Pharmacy
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAdrenaline
dc.subjectAnaesthesia
dc.subjectAnalgesic
dc.subjectCardiotoxicity
dc.subjectKetamine
dc.subjectNimesulide
dc.subject8 hydroxyguanine
dc.subjectcreatine kinase MB
dc.subjectglutathione
dc.subjectmalonaldehyde
dc.subjectnoradrenalin
dc.subjectreactive oxygen metabolite
dc.subjecttroponin I
dc.subjectadrenalectomy
dc.subjectanalgesia
dc.subjectanalgesic activity
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectDNA damage
dc.subjectfluorescent antibody technique
dc.subjectheart tissue
dc.subjecthigh performance liquid chromatography
dc.subjecthistopathology
dc.subjectnonhuman
dc.subjectoxidative stress
dc.subjectrat
dc.titlePreventive effect of nimesulide on ketamine induced cardiotoxicity and the useful interaction of nimesulide with ketamine
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.source.indexSCOPUS