Antinociceptive Activity and Redox Profile of the Monoterpenes (+)-Camphene, p-Cymene, and Geranyl Acetate in Experimental Models
Objective. To evaluate antinocicpetive and redox properties of the monoterpenes (+)-camphene, p-cymene, and geranyl acetate in in vivo and in vitro experimental models. Methods. Evaluation of the in vitro antioxidant activity of (+)-camphene, p-cymene, and geranyl acetate using different free radic...
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2013
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pubmed-36584122013-05-30 Antinociceptive Activity and Redox Profile of the Monoterpenes (+)-Camphene, p-Cymene, and Geranyl Acetate in Experimental Models Quintans-Júnior, Lucindo Moreira, José C. F. Pasquali, Matheus A. B. Rabie, Soheyla M. S. Pires, André S. Schröder, Rafael Rabelo, Thallita K. Santos, João P. A. Lima, Pollyana S. S. Cavalcanti, Sócrates C. H. Araújo, Adriano A. S. Quintans, Jullyana S. S. Gelain, Daniel P. Research Article Objective. To evaluate antinocicpetive and redox properties of the monoterpenes (+)-camphene, p-cymene, and geranyl acetate in in vivo and in vitro experimental models. Methods. Evaluation of the in vitro antioxidant activity of (+)-camphene, p-cymene, and geranyl acetate using different free radical-generating systems and evaluation of antinociceptive actions by acetic acid-induced writhing and formalin-induced nociception tests in mice. Results. p-Cymene has the strongest antinociceptive effect, but (+)-camphene and geranyl acetate also present significant activity at high doses (200 mg/kg). (+)-Camphene had the strongest antioxidant effect in vitro at TBARS and TRAP/TAR assays and also had the highest scavenging activities against different free radicals, such as hydroxyl and superoxide radicals. Sodium nitroprussiate-derived NO production was enhanced by (+)-camphene. Geranyl acetate and p-cymene also presented some antioxidant effects, but with a varying profile according the free radical-generating system studied. Conclusion. (+)-Camphene, p-cymene, and geranyl acetate may present pharmacological properties related to inflammation and pain-related processes, being potentially useful for development of new therapeutic strategies, with limited possibilities for p-cymene and geranyl acetate. Hindawi Publishing Corporation 2013-01-14 /pmc/articles/PMC3658412/ /pubmed/23724298 http://dx.doi.org/10.1155/2013/459530 Text en Copyright © 2013 Lucindo Quintans-Júnior 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. |
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Open Access Journal |
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US National Center for Biotechnology Information |
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NCBI PubMed |
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Online Access |
language |
English |
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Online |
author |
Quintans-Júnior, Lucindo Moreira, José C. F. Pasquali, Matheus A. B. Rabie, Soheyla M. S. Pires, André S. Schröder, Rafael Rabelo, Thallita K. Santos, João P. A. Lima, Pollyana S. S. Cavalcanti, Sócrates C. H. Araújo, Adriano A. S. Quintans, Jullyana S. S. Gelain, Daniel P. |
spellingShingle |
Quintans-Júnior, Lucindo Moreira, José C. F. Pasquali, Matheus A. B. Rabie, Soheyla M. S. Pires, André S. Schröder, Rafael Rabelo, Thallita K. Santos, João P. A. Lima, Pollyana S. S. Cavalcanti, Sócrates C. H. Araújo, Adriano A. S. Quintans, Jullyana S. S. Gelain, Daniel P. Antinociceptive Activity and Redox Profile of the Monoterpenes (+)-Camphene, p-Cymene, and Geranyl Acetate in Experimental Models |
author_facet |
Quintans-Júnior, Lucindo Moreira, José C. F. Pasquali, Matheus A. B. Rabie, Soheyla M. S. Pires, André S. Schröder, Rafael Rabelo, Thallita K. Santos, João P. A. Lima, Pollyana S. S. Cavalcanti, Sócrates C. H. Araújo, Adriano A. S. Quintans, Jullyana S. S. Gelain, Daniel P. |
author_sort |
Quintans-Júnior, Lucindo |
title |
Antinociceptive Activity and Redox Profile of the Monoterpenes (+)-Camphene, p-Cymene, and Geranyl Acetate in Experimental Models |
title_short |
Antinociceptive Activity and Redox Profile of the Monoterpenes (+)-Camphene, p-Cymene, and Geranyl Acetate in Experimental Models |
title_full |
Antinociceptive Activity and Redox Profile of the Monoterpenes (+)-Camphene, p-Cymene, and Geranyl Acetate in Experimental Models |
title_fullStr |
Antinociceptive Activity and Redox Profile of the Monoterpenes (+)-Camphene, p-Cymene, and Geranyl Acetate in Experimental Models |
title_full_unstemmed |
Antinociceptive Activity and Redox Profile of the Monoterpenes (+)-Camphene, p-Cymene, and Geranyl Acetate in Experimental Models |
title_sort |
antinociceptive activity and redox profile of the monoterpenes (+)-camphene, p-cymene, and geranyl acetate in experimental models |
description |
Objective. To evaluate antinocicpetive and redox properties of the monoterpenes (+)-camphene, p-cymene, and geranyl acetate in in vivo and in vitro experimental models. Methods. Evaluation of the in vitro antioxidant activity of (+)-camphene, p-cymene, and geranyl acetate using different free radical-generating systems and evaluation of antinociceptive actions by acetic acid-induced writhing and formalin-induced nociception tests in mice. Results. p-Cymene has the strongest antinociceptive effect, but (+)-camphene and geranyl acetate also present significant activity at high doses (200 mg/kg). (+)-Camphene had the strongest antioxidant effect in vitro at TBARS and TRAP/TAR assays and also had the highest scavenging activities against different free radicals, such as hydroxyl and superoxide radicals. Sodium nitroprussiate-derived NO production was enhanced by (+)-camphene. Geranyl acetate and p-cymene also presented some antioxidant effects, but with a varying profile according the free radical-generating system studied. Conclusion. (+)-Camphene, p-cymene, and geranyl acetate may present pharmacological properties related to inflammation and pain-related processes, being potentially useful for development of new therapeutic strategies, with limited possibilities for p-cymene and geranyl acetate. |
publisher |
Hindawi Publishing Corporation |
publishDate |
2013 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658412/ |
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1611979180947275776 |