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

Author:

Ok Seong-Ho123,Kang Dawon4,Lee Soo Hee12ORCID,Kim Hyun-Jin56,Ahn Seung Hyun7,Sohn Ju-Tae38ORCID

Affiliation:

1. Department of Anesthesiology and Pain Medicine, Gyeongsang National University, Changwon-si, Republic of Korea

2. Department of Anesthesiology and Pain Medicine, Gyeongsang National University College of Medicine, Jinju-si, Republic of Korea

3. Institute of Health Sciences, Gyeongsang National University, Jinju-si, Republic of Korea

4. Department of Physiology, Gyeongsang National University College of Medicine, Jinju-si, Republic of Korea

5. Division of Applied Life Sciences (BK21 four), Gyeongsang National University, Gyeongsang, Republic of Korea

6. Department of Food Science & Technology, Institute of Agriculture and Life Science, Gyeongsang National University, Gyeongsang, Republic of Korea

7. Department of Anesthesiology and Pain Medicine, Gyeongsang National University Hospital, Jinju-si, Republic of Korea

8. Department of Anesthesiology and Pain Medicine, Gyeongsang National University College of Medicine, Gyeongsang National University Hospital, Jinju-si, Republic of Korea

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.

Funder

National Research Foundation of Korea(NRF) grant funded by the Korea government

Biomedical research institute fund from the Gyeongsang National University Hospital

Publisher

SAGE Publications

Subject

Health, Toxicology and Mutagenesis,Toxicology,General Medicine

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