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The effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain

BACKGROUND: General anesthetics induce neuronal apoptosis in the immature brain. Regional anesthesia using local anesthetics can be an alternative to general anesthesia. Therefore, this study investigated the possible effect of lidocaine on neuronal apoptosis. METHODS: Fifty-one 7-day-old C57BL6 mic...

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Autores principales: Lee, Ji-Hyun, Park, Yong-Hee, Song, Hyun-Gul, Park, Hee-Pyoung, Kim, Hee-Soo, Kim, Chong-Sung, Kim, Jin-Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Anesthesiologists 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4252346/
https://www.ncbi.nlm.nih.gov/pubmed/25473463
http://dx.doi.org/10.4097/kjae.2014.67.5.334
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author Lee, Ji-Hyun
Park, Yong-Hee
Song, Hyun-Gul
Park, Hee-Pyoung
Kim, Hee-Soo
Kim, Chong-Sung
Kim, Jin-Tae
author_facet Lee, Ji-Hyun
Park, Yong-Hee
Song, Hyun-Gul
Park, Hee-Pyoung
Kim, Hee-Soo
Kim, Chong-Sung
Kim, Jin-Tae
author_sort Lee, Ji-Hyun
collection PubMed
description BACKGROUND: General anesthetics induce neuronal apoptosis in the immature brain. Regional anesthesia using local anesthetics can be an alternative to general anesthesia. Therefore, this study investigated the possible effect of lidocaine on neuronal apoptosis. METHODS: Fifty-one 7-day-old C57BL6 mice were allocated into control (group C), lidocaine (group L), lidocaine plus midazolam (group LM) and isoflurane (group I) groups. Group C received normal saline administration. Groups L and LM were injected with lidocaine (4 mg/kg, subcutaneously) only and the same dose of lidocaine plus midazolam (9 mg/kg, subcutaneously). Group I was exposed to 0.75 vol% isoflurane for 6 h. After 6 h, apoptotic neurodegeneration was assessed using caspase-3 immunostaining and terminal deoxynucleotidyl transferase dUTP nick-end labelling (TUNEL) staining. RESULTS: For the entire brain section, neuronal cells exhibiting caspase-3 activation were observed more frequently in group I than in group C (P < 0.001). In the thalamus, apoptosis of group L was more frequent than that of group C (P < 0.001), but less freqent than that of groups LM and I (P = 0.0075 and P < 0.001, respectively). In the cortex, group I experienced more apoptosis than group L and C (all Ps < 0.001). On TUNEL staining, the difference in apoptosis between the lidocaine and control groups was marginal (P = 0.05). CONCLUSIONS: Lidocaine induced minimal apoptosis in the developing brain compared with isoflurane and lidocaine plus midazolam. However, we cannot fully exclude the possible adverse effect of subcutaneously administered lidocaine on the developing brain.
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spelling pubmed-42523462014-12-03 The effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain Lee, Ji-Hyun Park, Yong-Hee Song, Hyun-Gul Park, Hee-Pyoung Kim, Hee-Soo Kim, Chong-Sung Kim, Jin-Tae Korean J Anesthesiol Experimental Research Article BACKGROUND: General anesthetics induce neuronal apoptosis in the immature brain. Regional anesthesia using local anesthetics can be an alternative to general anesthesia. Therefore, this study investigated the possible effect of lidocaine on neuronal apoptosis. METHODS: Fifty-one 7-day-old C57BL6 mice were allocated into control (group C), lidocaine (group L), lidocaine plus midazolam (group LM) and isoflurane (group I) groups. Group C received normal saline administration. Groups L and LM were injected with lidocaine (4 mg/kg, subcutaneously) only and the same dose of lidocaine plus midazolam (9 mg/kg, subcutaneously). Group I was exposed to 0.75 vol% isoflurane for 6 h. After 6 h, apoptotic neurodegeneration was assessed using caspase-3 immunostaining and terminal deoxynucleotidyl transferase dUTP nick-end labelling (TUNEL) staining. RESULTS: For the entire brain section, neuronal cells exhibiting caspase-3 activation were observed more frequently in group I than in group C (P < 0.001). In the thalamus, apoptosis of group L was more frequent than that of group C (P < 0.001), but less freqent than that of groups LM and I (P = 0.0075 and P < 0.001, respectively). In the cortex, group I experienced more apoptosis than group L and C (all Ps < 0.001). On TUNEL staining, the difference in apoptosis between the lidocaine and control groups was marginal (P = 0.05). CONCLUSIONS: Lidocaine induced minimal apoptosis in the developing brain compared with isoflurane and lidocaine plus midazolam. However, we cannot fully exclude the possible adverse effect of subcutaneously administered lidocaine on the developing brain. The Korean Society of Anesthesiologists 2014-11 2014-11-26 /pmc/articles/PMC4252346/ /pubmed/25473463 http://dx.doi.org/10.4097/kjae.2014.67.5.334 Text en Copyright © the Korean Society of Anesthesiologists, 2014 http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Experimental Research Article
Lee, Ji-Hyun
Park, Yong-Hee
Song, Hyun-Gul
Park, Hee-Pyoung
Kim, Hee-Soo
Kim, Chong-Sung
Kim, Jin-Tae
The effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain
title The effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain
title_full The effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain
title_fullStr The effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain
title_full_unstemmed The effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain
title_short The effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain
title_sort effect of lidocaine on apoptotic neurodegeneration in the developing mouse brain
topic Experimental Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4252346/
https://www.ncbi.nlm.nih.gov/pubmed/25473463
http://dx.doi.org/10.4097/kjae.2014.67.5.334
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