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Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models

The objective of the present study was to evaluate the antinociceptive effects of phytol using chemical and thermal models of nociception in mice and to assess its antioxidant effects in vitro. Phytol was administered intraperitoneally (i.p.) to mice at doses of 25, 50, 100, and 200 mg/kg. In the ac...

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Autores principales: Santos, Camila Carolina de Menezes Patrício, Salvadori, Mirian Stiebbe, Mota, Vanine Gomes, Costa, Luciana Muratori, de Almeida, Antonia Amanda Cardoso, de Oliveira, Guilherme Antônio Lopes, Costa, Jéssica Pereira, de Sousa, Damião Pergentino, de Freitas, Rivelilson Mendes, de Almeida, Reinaldo Nóbrega
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437258/
https://www.ncbi.nlm.nih.gov/pubmed/26317107
http://dx.doi.org/10.1155/2013/949452
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author Santos, Camila Carolina de Menezes Patrício
Salvadori, Mirian Stiebbe
Mota, Vanine Gomes
Costa, Luciana Muratori
de Almeida, Antonia Amanda Cardoso
de Oliveira, Guilherme Antônio Lopes
Costa, Jéssica Pereira
de Sousa, Damião Pergentino
de Freitas, Rivelilson Mendes
de Almeida, Reinaldo Nóbrega
author_facet Santos, Camila Carolina de Menezes Patrício
Salvadori, Mirian Stiebbe
Mota, Vanine Gomes
Costa, Luciana Muratori
de Almeida, Antonia Amanda Cardoso
de Oliveira, Guilherme Antônio Lopes
Costa, Jéssica Pereira
de Sousa, Damião Pergentino
de Freitas, Rivelilson Mendes
de Almeida, Reinaldo Nóbrega
author_sort Santos, Camila Carolina de Menezes Patrício
collection PubMed
description The objective of the present study was to evaluate the antinociceptive effects of phytol using chemical and thermal models of nociception in mice and to assess its antioxidant effects in vitro. Phytol was administered intraperitoneally (i.p.) to mice at doses of 25, 50, 100, and 200 mg/kg. In the acetic acid-induced writhing test, phytol significantly reduced the number of contortions compared to the control group (P < 0.001). In the formalin test, phytol reduced significantly the amount of time spent in paw licking in both phases (the neurogenic and inflammatory phases), this effect being more pronounced in the second phase (P < 0.001). Phytol also provoked a significant increase in latency in the hot plate test. These antinociceptive effects did not impaire the motor performance, as shown in the rotarod test. Phytol demonstrated a strong antioxidant effect in vitro in its capacity to remove hydroxyl radicals and nitric oxide as well as to prevent the formation of thiobarbituric acid reactive substances (TBARS). Taken as a whole, these results show the pronounced antinociceptive effects of phytol in the nociception models used, both through its central and peripheral actions, but also its antioxidant properties demonstrated in the in vitro methods used.
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spelling pubmed-44372582015-08-27 Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models Santos, Camila Carolina de Menezes Patrício Salvadori, Mirian Stiebbe Mota, Vanine Gomes Costa, Luciana Muratori de Almeida, Antonia Amanda Cardoso de Oliveira, Guilherme Antônio Lopes Costa, Jéssica Pereira de Sousa, Damião Pergentino de Freitas, Rivelilson Mendes de Almeida, Reinaldo Nóbrega Neurosci J Research Article The objective of the present study was to evaluate the antinociceptive effects of phytol using chemical and thermal models of nociception in mice and to assess its antioxidant effects in vitro. Phytol was administered intraperitoneally (i.p.) to mice at doses of 25, 50, 100, and 200 mg/kg. In the acetic acid-induced writhing test, phytol significantly reduced the number of contortions compared to the control group (P < 0.001). In the formalin test, phytol reduced significantly the amount of time spent in paw licking in both phases (the neurogenic and inflammatory phases), this effect being more pronounced in the second phase (P < 0.001). Phytol also provoked a significant increase in latency in the hot plate test. These antinociceptive effects did not impaire the motor performance, as shown in the rotarod test. Phytol demonstrated a strong antioxidant effect in vitro in its capacity to remove hydroxyl radicals and nitric oxide as well as to prevent the formation of thiobarbituric acid reactive substances (TBARS). Taken as a whole, these results show the pronounced antinociceptive effects of phytol in the nociception models used, both through its central and peripheral actions, but also its antioxidant properties demonstrated in the in vitro methods used. Hindawi Publishing Corporation 2013 2013-06-11 /pmc/articles/PMC4437258/ /pubmed/26317107 http://dx.doi.org/10.1155/2013/949452 Text en Copyright © 2013 Camila Carolina de Menezes Patrício Santos et al. https://creativecommons.org/licenses/by/3.0/ 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
Santos, Camila Carolina de Menezes Patrício
Salvadori, Mirian Stiebbe
Mota, Vanine Gomes
Costa, Luciana Muratori
de Almeida, Antonia Amanda Cardoso
de Oliveira, Guilherme Antônio Lopes
Costa, Jéssica Pereira
de Sousa, Damião Pergentino
de Freitas, Rivelilson Mendes
de Almeida, Reinaldo Nóbrega
Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models
title Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models
title_full Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models
title_fullStr Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models
title_full_unstemmed Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models
title_short Antinociceptive and Antioxidant Activities of Phytol In Vivo and In Vitro Models
title_sort antinociceptive and antioxidant activities of phytol in vivo and in vitro models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437258/
https://www.ncbi.nlm.nih.gov/pubmed/26317107
http://dx.doi.org/10.1155/2013/949452
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