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Lipid emulsions attenuate the inhibition of carnitine acylcarnitine translocase induced by toxic doses of local anesthetics in rat cardiomyoblastsopen access

Authors
Ok, Seong-HoKang, DawonLee, Soo HeeKim, Hyun-JinAhn, Seung HyunSohn, Ju-Tae
Issue Date
5-Jan-2022
Publisher
SAGE PUBLICATIONS LTD
Keywords
lipid emulsion; carnitine palmitoyltransferase; carnitine acylcarnitine translocase; local anesthetic; levobupivacaine; bupivacaine; ropivacaine; reactive oxygen species
Citation
HUMAN & EXPERIMENTAL TOXICOLOGY, v.41
Indexed
SCIE
SCOPUS
Journal Title
HUMAN & EXPERIMENTAL TOXICOLOGY
Volume
41
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/1755
DOI
10.1177/09603271211065978
ISSN
0960-3271
Abstract
The aim of this study was to examine the effects of lipid emulsions on carnitine palmitoyltransferase I (CPT-I), carnitine acylcarnitine translocase (CACT), carnitine palmitoyltransferase II (CPT-II), and the mitochondrial dysfunctions induced by toxic doses of local anesthetics in H9c2 rat cardiomyoblasts. The effects of local anesthetics and lipid emulsions on the activities of CPT-I, CACT, and CPT-II, and concentrations of local anesthetics were examined. The effects of lipid emulsions, N-acetyl-L-cysteine (NAC), and mitotempo on the bupivacaine-induced changes in cell viability, reactive oxygen species (ROS) levels, mitochondrial membrane potential (MMP), and intracellular calcium levels were examined. CACT, without significantly altering CPT-I and CPT-II, was inhibited by toxic concentration of local anesthetics. The levobupivacaine- and bupivacaine-induced inhibition of CACT was attenuated by all concentrations of lipid emulsion, whereas the ropivacaine-induced inhibition of CACT was attenuated by medium and high concentrations of lipid emulsion. The concentration of levobupivacaine was slightly attenuated by lipid emulsion. The bupivacaine-induced increase of ROS and calcium and the bupivacaine-induced decrease of MMP were attenuated by ROS scavengers NAC and mitotempo, and the lipid emulsion. Collectively, these results suggested that the lipid emulsion attenuated the levobupivacaine-induced inhibition of CACT, probably through the lipid emulsion-mediated sequestration of levobupivacaine.
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