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Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extract

BACKGROUND: Tabebuia avellanedae is a tree from the Bignoniaceae family. Commonly know as "pau d'arco" in Brazil, its inner bark is used as analgesic, anti-inflammatory, antineoplasic and diuretic at the Brazilian northeast. A validation of the plant usage has not been previously perf...

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Autores principales: de Miranda, Fábio Guilherme Gonçalves, Vilar, Jeane Carvalho, Alves, Ivana Andréa Nunes, Cavalcanti, Sócrates Cabral de Holanda, Antoniolli, Ângelo Roberto
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC56902/
https://www.ncbi.nlm.nih.gov/pubmed/11574048
http://dx.doi.org/10.1186/1471-2210-1-6
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author de Miranda, Fábio Guilherme Gonçalves
Vilar, Jeane Carvalho
Alves, Ivana Andréa Nunes
Cavalcanti, Sócrates Cabral de Holanda
Antoniolli, Ângelo Roberto
author_facet de Miranda, Fábio Guilherme Gonçalves
Vilar, Jeane Carvalho
Alves, Ivana Andréa Nunes
Cavalcanti, Sócrates Cabral de Holanda
Antoniolli, Ângelo Roberto
author_sort de Miranda, Fábio Guilherme Gonçalves
collection PubMed
description BACKGROUND: Tabebuia avellanedae is a tree from the Bignoniaceae family. Commonly know as "pau d'arco" in Brazil, its inner bark is used as analgesic, anti-inflammatory, antineoplasic and diuretic at the Brazilian northeast. A validation of the plant usage has not been previously performed. RESULTS: Antinociceptive and antiedematogenic effects of Tabebuia avellanedae Lor. ex Griseb. inner bark were measured by nociceptive experimental models in mice. A rat paw edema test induced by carrageenan (1%) was also performed in rats to access the plant's antiedematogenic effect. The inner bark aqueous extract, administered via oral in three different concentration, namely 100, 200 and 400 mg/Kg, reduced the nociception produced by acetic acid (0.6% in water, i.p.) by 49.9%, 63.7% and 43.8%, respectively. The aqueous extract (200 and 400 mg/Kg, p.o.) reduced formalin (1%) effects only at the second phase of the experiment by 49.3% and 53.7%, respectively. Naloxone (5 mg/Kg, i.p.) was not able to revert the extract effect, however caffeine (10 mg/Kg, i.p.) reverted its effect by 19.8% at the second phase of the formalin test. The aqueous extract (200 mg/Kg, p.o.) inhibited edema by 12.9% when we used the rat paw edema model. The acute toxicity was low in mice. CONCLUSION: The T. avellanedae inner bark aqueous extract presented antinociceptive and antiedematogenic activities at the used models, with a possible antinociceptive effect associated to the adenosine system.
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spelling pubmed-569022001-10-01 Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extract de Miranda, Fábio Guilherme Gonçalves Vilar, Jeane Carvalho Alves, Ivana Andréa Nunes Cavalcanti, Sócrates Cabral de Holanda Antoniolli, Ângelo Roberto BMC Pharmacol Research Article BACKGROUND: Tabebuia avellanedae is a tree from the Bignoniaceae family. Commonly know as "pau d'arco" in Brazil, its inner bark is used as analgesic, anti-inflammatory, antineoplasic and diuretic at the Brazilian northeast. A validation of the plant usage has not been previously performed. RESULTS: Antinociceptive and antiedematogenic effects of Tabebuia avellanedae Lor. ex Griseb. inner bark were measured by nociceptive experimental models in mice. A rat paw edema test induced by carrageenan (1%) was also performed in rats to access the plant's antiedematogenic effect. The inner bark aqueous extract, administered via oral in three different concentration, namely 100, 200 and 400 mg/Kg, reduced the nociception produced by acetic acid (0.6% in water, i.p.) by 49.9%, 63.7% and 43.8%, respectively. The aqueous extract (200 and 400 mg/Kg, p.o.) reduced formalin (1%) effects only at the second phase of the experiment by 49.3% and 53.7%, respectively. Naloxone (5 mg/Kg, i.p.) was not able to revert the extract effect, however caffeine (10 mg/Kg, i.p.) reverted its effect by 19.8% at the second phase of the formalin test. The aqueous extract (200 mg/Kg, p.o.) inhibited edema by 12.9% when we used the rat paw edema model. The acute toxicity was low in mice. CONCLUSION: The T. avellanedae inner bark aqueous extract presented antinociceptive and antiedematogenic activities at the used models, with a possible antinociceptive effect associated to the adenosine system. BioMed Central 2001-09-13 /pmc/articles/PMC56902/ /pubmed/11574048 http://dx.doi.org/10.1186/1471-2210-1-6 Text en Copyright © 2001 de Miranda et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
de Miranda, Fábio Guilherme Gonçalves
Vilar, Jeane Carvalho
Alves, Ivana Andréa Nunes
Cavalcanti, Sócrates Cabral de Holanda
Antoniolli, Ângelo Roberto
Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extract
title Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extract
title_full Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extract
title_fullStr Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extract
title_full_unstemmed Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extract
title_short Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extract
title_sort antinociceptive and antiedematogenic properties and acute toxicity of tabebuia avellanedae lor. ex griseb. inner bark aqueous extract
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC56902/
https://www.ncbi.nlm.nih.gov/pubmed/11574048
http://dx.doi.org/10.1186/1471-2210-1-6
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