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Antinociceptive Activity of Trichilia catigua Hydroalcoholic Extract: New Evidence on Its Dopaminergic Effects

Trichilia catigua is a native plant of Brazil; its barks are used by some local pharmaceutical companies to prepare tonic drinks, such as Catuama. The present study was addressed to evaluate the effects of T. catigua hydroalcoholic extract in mouse nociception behavioral models, and to evaluate the...

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Autores principales: Viana, Alice F., Maciel, Izaque S., Motta, Emerson M., Leal, Paulo C., Pianowski, Luiz, Campos, Maria M., Calixto, João B.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095233/
https://www.ncbi.nlm.nih.gov/pubmed/19815648
http://dx.doi.org/10.1093/ecam/nep144
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author Viana, Alice F.
Maciel, Izaque S.
Motta, Emerson M.
Leal, Paulo C.
Pianowski, Luiz
Campos, Maria M.
Calixto, João B.
author_facet Viana, Alice F.
Maciel, Izaque S.
Motta, Emerson M.
Leal, Paulo C.
Pianowski, Luiz
Campos, Maria M.
Calixto, João B.
author_sort Viana, Alice F.
collection PubMed
description Trichilia catigua is a native plant of Brazil; its barks are used by some local pharmaceutical companies to prepare tonic drinks, such as Catuama. The present study was addressed to evaluate the effects of T. catigua hydroalcoholic extract in mouse nociception behavioral models, and to evaluate the possible mechanisms involved in its actions. Male Swiss mice were submitted to hot-plate, writhing and von Frey tests, after oral treatment with T. catigua extract (200 mg kg(−1), p.o.). The extract displayed antinociceptive effect in all three models. For characterization of the mechanisms involved in the antinociceptive action of the extract, the following pharmacological treatments were done: naloxone (2.5 mg kg(−1), s.c.), SR141716A (10 mg kg(−1), i.p.), SCH23390 (15 μg kg(−1), i.p.), sulpiride (50 mg kg(−1), i.p.), prazosin (1 mg kg(−1), i.p.), bicuculline (1 mg kg(−1), i.p.) or dl-p-chlorophenylalanine methyl ester (PCPA, 100 mg kg(−1), i.p.). In these experiments, the action of T. catigua extract was evaluated in the hot-plate test. The treatment with SCH23390 completely prevented the antinociceptive effect, while naloxone partially prevented it. The possible involvement of the dopaminergic system in the actions of T. catigua extract was substantiated by data showing the potentiation of apomorphine-induced hypothermia and by the prevention of haloperidol-induced catalepsy. In conclusion, the antinociceptive effects of T. catigua extract seem to be mainly associated with the activation of dopaminergic system and, to a lesser extent, through interaction with opioid pathway.
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spelling pubmed-30952332011-05-23 Antinociceptive Activity of Trichilia catigua Hydroalcoholic Extract: New Evidence on Its Dopaminergic Effects Viana, Alice F. Maciel, Izaque S. Motta, Emerson M. Leal, Paulo C. Pianowski, Luiz Campos, Maria M. Calixto, João B. Evid Based Complement Alternat Med Original Article Trichilia catigua is a native plant of Brazil; its barks are used by some local pharmaceutical companies to prepare tonic drinks, such as Catuama. The present study was addressed to evaluate the effects of T. catigua hydroalcoholic extract in mouse nociception behavioral models, and to evaluate the possible mechanisms involved in its actions. Male Swiss mice were submitted to hot-plate, writhing and von Frey tests, after oral treatment with T. catigua extract (200 mg kg(−1), p.o.). The extract displayed antinociceptive effect in all three models. For characterization of the mechanisms involved in the antinociceptive action of the extract, the following pharmacological treatments were done: naloxone (2.5 mg kg(−1), s.c.), SR141716A (10 mg kg(−1), i.p.), SCH23390 (15 μg kg(−1), i.p.), sulpiride (50 mg kg(−1), i.p.), prazosin (1 mg kg(−1), i.p.), bicuculline (1 mg kg(−1), i.p.) or dl-p-chlorophenylalanine methyl ester (PCPA, 100 mg kg(−1), i.p.). In these experiments, the action of T. catigua extract was evaluated in the hot-plate test. The treatment with SCH23390 completely prevented the antinociceptive effect, while naloxone partially prevented it. The possible involvement of the dopaminergic system in the actions of T. catigua extract was substantiated by data showing the potentiation of apomorphine-induced hypothermia and by the prevention of haloperidol-induced catalepsy. In conclusion, the antinociceptive effects of T. catigua extract seem to be mainly associated with the activation of dopaminergic system and, to a lesser extent, through interaction with opioid pathway. Hindawi Publishing Corporation 2011 2011-04-14 /pmc/articles/PMC3095233/ /pubmed/19815648 http://dx.doi.org/10.1093/ecam/nep144 Text en Copyright © 2011 Alice F. Viana 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 Original Article
Viana, Alice F.
Maciel, Izaque S.
Motta, Emerson M.
Leal, Paulo C.
Pianowski, Luiz
Campos, Maria M.
Calixto, João B.
Antinociceptive Activity of Trichilia catigua Hydroalcoholic Extract: New Evidence on Its Dopaminergic Effects
title Antinociceptive Activity of Trichilia catigua Hydroalcoholic Extract: New Evidence on Its Dopaminergic Effects
title_full Antinociceptive Activity of Trichilia catigua Hydroalcoholic Extract: New Evidence on Its Dopaminergic Effects
title_fullStr Antinociceptive Activity of Trichilia catigua Hydroalcoholic Extract: New Evidence on Its Dopaminergic Effects
title_full_unstemmed Antinociceptive Activity of Trichilia catigua Hydroalcoholic Extract: New Evidence on Its Dopaminergic Effects
title_short Antinociceptive Activity of Trichilia catigua Hydroalcoholic Extract: New Evidence on Its Dopaminergic Effects
title_sort antinociceptive activity of trichilia catigua hydroalcoholic extract: new evidence on its dopaminergic effects
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095233/
https://www.ncbi.nlm.nih.gov/pubmed/19815648
http://dx.doi.org/10.1093/ecam/nep144
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