Cardioprotective effect of intravenous lipid emulsion in bupivacaine- induced experimental cardiac toxicity

The intravenous lipid emulsion (ILE) therapy is known to alleviate clinical symptoms in cases of bupivacaine-induced cardiac toxicity. However, there is insufficient information regarding histopathological damage. This study aimed to investigate whether the use of ILE therapy in rats with experiment...

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Main Authors: Nezir YILMAZ, Mevlüt DOĞUKAN, Ahmet TÜRK, Fadime TOSUN
Format: Article
Language:English
Published: Kafkas University, Faculty of Veterinary Medicine 2023-10-01
Series:Kafkas Universitesi Veteriner Fakültesi Dergisi
Subjects:
Online Access:https://vetdergikafkas.org/pdf.php?id=3038
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author Nezir YILMAZ
Mevlüt DOĞUKAN
Ahmet TÜRK
Fadime TOSUN
author_facet Nezir YILMAZ
Mevlüt DOĞUKAN
Ahmet TÜRK
Fadime TOSUN
author_sort Nezir YILMAZ
collection DOAJ
description The intravenous lipid emulsion (ILE) therapy is known to alleviate clinical symptoms in cases of bupivacaine-induced cardiac toxicity. However, there is insufficient information regarding histopathological damage. This study aimed to investigate whether the use of ILE therapy in rats with experimentally induced bupivacaine-related cardiac toxicity can ameliorate histopathological damage. 28 Wistar albino rats were divided into four groups: control (A), lipid (B), bupivacaine (C), and bupivacaine + lipid (D). After providing monitoring in all groups, group B received 1.5 mL ILE + 0.25 μg/kg/min ILE infusion, group C received 3 μg/kg/min bupivacaine infusion, and group D received 3 μg/kg/min bupivacaine infusion followed by 1.5 mL ILE + 0.25 μg/kg/min ILE infusion after observing cardiac toxicity. Heart rate and respiratory rate were recorded. Blood samples were collected post-procedure to measure LDH, CK-MB, and troponin levels. Cardiac tissue samples were obtained for histopathological examination. There was no significant difference in baseline heart rate and respiratory rate among the groups (P>0.05). However, in the second measurements, heart rate and respiratory rate were higher in group D compared to group C (P<0.05). LDH and CK-MB levels were higher in group C compared to the other groups (P<0.05). Irisin and asprosin scores were higher in group D compared to the other groups (P<0.05). ILE was found to have a cardioprotective effect in the treatment of bupivacaine-induced cardiac toxicity, as it improved both clinical and laboratory parameters. However, histologically, cardiac damage persisted.
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spelling doaj.art-c36f884a8bfa42aa834857541416bf642023-12-05T21:27:26ZengKafkas University, Faculty of Veterinary MedicineKafkas Universitesi Veteriner Fakültesi Dergisi1309-22512023-10-0129668368810.9775/kvfd.2023.301773038Cardioprotective effect of intravenous lipid emulsion in bupivacaine- induced experimental cardiac toxicityNezir YILMAZ0Mevlüt DOĞUKAN1Ahmet TÜRK2Fadime TOSUN3AdıyamanUniversity, Faculty of Medicine, Anesthesiology and Reanimation Department, TR-02100 Adıyaman - TÜRKİYEAdıyamanUniversity, Faculty of Medicine, Anesthesiology and Reanimation Department, TR-02100 Adıyaman - TÜRKİYEAdıyamanUniversity, Faculty of Medicine, Histology and Embryology Department, TR-02100 Adıyaman - TÜRKİYEAdıyamanUniversity, Faculty of Medicine, Anesthesiology and Reanimation Department, TR-02100 Adıyaman - TÜRKİYEThe intravenous lipid emulsion (ILE) therapy is known to alleviate clinical symptoms in cases of bupivacaine-induced cardiac toxicity. However, there is insufficient information regarding histopathological damage. This study aimed to investigate whether the use of ILE therapy in rats with experimentally induced bupivacaine-related cardiac toxicity can ameliorate histopathological damage. 28 Wistar albino rats were divided into four groups: control (A), lipid (B), bupivacaine (C), and bupivacaine + lipid (D). After providing monitoring in all groups, group B received 1.5 mL ILE + 0.25 μg/kg/min ILE infusion, group C received 3 μg/kg/min bupivacaine infusion, and group D received 3 μg/kg/min bupivacaine infusion followed by 1.5 mL ILE + 0.25 μg/kg/min ILE infusion after observing cardiac toxicity. Heart rate and respiratory rate were recorded. Blood samples were collected post-procedure to measure LDH, CK-MB, and troponin levels. Cardiac tissue samples were obtained for histopathological examination. There was no significant difference in baseline heart rate and respiratory rate among the groups (P>0.05). However, in the second measurements, heart rate and respiratory rate were higher in group D compared to group C (P<0.05). LDH and CK-MB levels were higher in group C compared to the other groups (P<0.05). Irisin and asprosin scores were higher in group D compared to the other groups (P<0.05). ILE was found to have a cardioprotective effect in the treatment of bupivacaine-induced cardiac toxicity, as it improved both clinical and laboratory parameters. However, histologically, cardiac damage persisted.https://vetdergikafkas.org/pdf.php?id=3038bupivacainecardiac toxicityhistopathologylipid emulsion
spellingShingle Nezir YILMAZ
Mevlüt DOĞUKAN
Ahmet TÜRK
Fadime TOSUN
Cardioprotective effect of intravenous lipid emulsion in bupivacaine- induced experimental cardiac toxicity
Kafkas Universitesi Veteriner Fakültesi Dergisi
bupivacaine
cardiac toxicity
histopathology
lipid emulsion
title Cardioprotective effect of intravenous lipid emulsion in bupivacaine- induced experimental cardiac toxicity
title_full Cardioprotective effect of intravenous lipid emulsion in bupivacaine- induced experimental cardiac toxicity
title_fullStr Cardioprotective effect of intravenous lipid emulsion in bupivacaine- induced experimental cardiac toxicity
title_full_unstemmed Cardioprotective effect of intravenous lipid emulsion in bupivacaine- induced experimental cardiac toxicity
title_short Cardioprotective effect of intravenous lipid emulsion in bupivacaine- induced experimental cardiac toxicity
title_sort cardioprotective effect of intravenous lipid emulsion in bupivacaine induced experimental cardiac toxicity
topic bupivacaine
cardiac toxicity
histopathology
lipid emulsion
url https://vetdergikafkas.org/pdf.php?id=3038
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AT ahmetturk cardioprotectiveeffectofintravenouslipidemulsioninbupivacaineinducedexperimentalcardiactoxicity
AT fadimetosun cardioprotectiveeffectofintravenouslipidemulsioninbupivacaineinducedexperimentalcardiactoxicity