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Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve

The racemate linalool and its levogyrus enantiomer [(−)-LIN] are present in many essential oils and possess several pharmacological activities, such as antinociceptive and anti-inflammatory. In this work, the effects of essential oil obtained from the cultivation of the Ocimum basilicum L. (EOOb) de...

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Autores principales: Medeiros Venancio, Antonio, Ferreira-da-Silva, Francisco Walber, da Silva-Alves, Kerly Shamyra, de Carvalho Pimentel, Hugo, Macêdo Lima, Matheus, Fraga de Santana, Michele, Barreto Alves, Péricles, Batista da Silva, Givanildo, Leal-Cardoso, José Henrique, Marchioro, Murilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944029/
https://www.ncbi.nlm.nih.gov/pubmed/27446227
http://dx.doi.org/10.1155/2016/9012605
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author Medeiros Venancio, Antonio
Ferreira-da-Silva, Francisco Walber
da Silva-Alves, Kerly Shamyra
de Carvalho Pimentel, Hugo
Macêdo Lima, Matheus
Fraga de Santana, Michele
Barreto Alves, Péricles
Batista da Silva, Givanildo
Leal-Cardoso, José Henrique
Marchioro, Murilo
author_facet Medeiros Venancio, Antonio
Ferreira-da-Silva, Francisco Walber
da Silva-Alves, Kerly Shamyra
de Carvalho Pimentel, Hugo
Macêdo Lima, Matheus
Fraga de Santana, Michele
Barreto Alves, Péricles
Batista da Silva, Givanildo
Leal-Cardoso, José Henrique
Marchioro, Murilo
author_sort Medeiros Venancio, Antonio
collection PubMed
description The racemate linalool and its levogyrus enantiomer [(−)-LIN] are present in many essential oils and possess several pharmacological activities, such as antinociceptive and anti-inflammatory. In this work, the effects of essential oil obtained from the cultivation of the Ocimum basilicum L. (EOOb) derived from Germplasm Bank rich in (−)-LIN content in the excitability of peripheral nervous system were studied. We used rat sciatic nerve to investigate the EOOb and (−)-LIN effects on neuron excitability and the extracellular recording technique was used to register the compound action potential (CAP). EOOb and (−)-LIN blocked the CAP in a concentration-dependent way and these effects were reversible after washout. EOOb blocked positive amplitude of 1st and 2nd CAP components with IC(50) of 0.38 ± 0.2 and 0.17 ± 0.0 mg/mL, respectively. For (−)-LIN, these values were 0.23 ± 0.0 and 0.13 ± 0.0 mg/mL. Both components reduced the conduction velocity of CAP and the 2nd component seems to be more affected than the 1st component. In conclusion EOOb and (−)-LIN inhibited the excitability of peripheral nervous system in a similar way and potency, revealing that the effects of EOOb on excitability are due to the presence of (−)-LIN in the essential oil.
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spelling pubmed-49440292016-07-21 Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve Medeiros Venancio, Antonio Ferreira-da-Silva, Francisco Walber da Silva-Alves, Kerly Shamyra de Carvalho Pimentel, Hugo Macêdo Lima, Matheus Fraga de Santana, Michele Barreto Alves, Péricles Batista da Silva, Givanildo Leal-Cardoso, José Henrique Marchioro, Murilo Evid Based Complement Alternat Med Research Article The racemate linalool and its levogyrus enantiomer [(−)-LIN] are present in many essential oils and possess several pharmacological activities, such as antinociceptive and anti-inflammatory. In this work, the effects of essential oil obtained from the cultivation of the Ocimum basilicum L. (EOOb) derived from Germplasm Bank rich in (−)-LIN content in the excitability of peripheral nervous system were studied. We used rat sciatic nerve to investigate the EOOb and (−)-LIN effects on neuron excitability and the extracellular recording technique was used to register the compound action potential (CAP). EOOb and (−)-LIN blocked the CAP in a concentration-dependent way and these effects were reversible after washout. EOOb blocked positive amplitude of 1st and 2nd CAP components with IC(50) of 0.38 ± 0.2 and 0.17 ± 0.0 mg/mL, respectively. For (−)-LIN, these values were 0.23 ± 0.0 and 0.13 ± 0.0 mg/mL. Both components reduced the conduction velocity of CAP and the 2nd component seems to be more affected than the 1st component. In conclusion EOOb and (−)-LIN inhibited the excitability of peripheral nervous system in a similar way and potency, revealing that the effects of EOOb on excitability are due to the presence of (−)-LIN in the essential oil. Hindawi Publishing Corporation 2016 2016-06-30 /pmc/articles/PMC4944029/ /pubmed/27446227 http://dx.doi.org/10.1155/2016/9012605 Text en Copyright © 2016 Antonio Medeiros Venancio et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Medeiros Venancio, Antonio
Ferreira-da-Silva, Francisco Walber
da Silva-Alves, Kerly Shamyra
de Carvalho Pimentel, Hugo
Macêdo Lima, Matheus
Fraga de Santana, Michele
Barreto Alves, Péricles
Batista da Silva, Givanildo
Leal-Cardoso, José Henrique
Marchioro, Murilo
Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve
title Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve
title_full Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve
title_fullStr Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve
title_full_unstemmed Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve
title_short Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve
title_sort essential oil of ocimum basilicum l. and (−)-linalool blocks the excitability of rat sciatic nerve
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944029/
https://www.ncbi.nlm.nih.gov/pubmed/27446227
http://dx.doi.org/10.1155/2016/9012605
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